update version to 1.9, and date to today.

[jalview-manual.git] / TheJalviewTutorial.tex

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\title{Jalview 2.5: A manual and introductory tutorial }
\author{David Martin, James Procter, Andrew Waterhouse, Saif Shehata, Nancy Giang,Suzanne Duce and Geoff Barton}
\date{Manual version 1.2.3 6th May 2011}

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\begin{document}


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\begin{center}

{\Huge
 
Jalview 2.10.1}
\vspace{0.5in}
{\huge 

Manual and  Introductory Tutorial }

\vspace{2.2in}

{\large

David Martin, James Procter 

Andrew Waterhouse, Saif Shehata, Nancy Giang 

Mungo Carstairs, Charles Ofoegbu, Kira Mour\~{a}o

Suzanne Duce and Geoff Barton 

}

\vspace{0.9in}

School of Life Sciences, University of Dundee

Dundee, Scotland DD1 5EH, UK

\vspace{2in}
Manual Version 1.9

% for CLS lifesci course 2017 & St Andrews course
%  Remaining items are AACon, RNA visualization/editing and Protein disorder analysis exercises.
20th February 2017

\end{center}

%\newpage

\clearemptydoublepage

% ($Revision$) 11th October 2010.}
% TODO revise for 2.6

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\tableofcontents 
%\clearemptydoublepage
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% \newpage
% \listoftables 
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\chapter{Basics}
\label{jalviewbasics}
\section{Introduction}
\subsection{Jalview}
Jalview is a multiple sequence alignment viewer, editor and analysis tool.
Jalview is designed to be platform independent (running on Mac, MS Windows, Linux
and any other platforms that support Java). Jalview is capable of editing and
analysing large alignments (thousands of sequences) with minimal degradation in
performance, and able to show multiple integrated views of the alignment and
other data. Jalview can read and write many common sequence formats including
FASTA, Clustal, MSF(GCG) and PIR.


There are two types of Jalview program. The {\bf Jalview Desktop} is a standalone 
application that provides powerful editing, visualization, annotation and
analysis capabilities. The {\bf JalviewLite} applet has the same core
visualization, editing and analysis capabilities as the desktop, without the
desktop's webservice and figure generation capabilities. It is designed to be
embedded in a web page,\footnote{A demonstration version of Jalview (Jalview Micro
Edition) also runs on a mobile phone but the functionality is limited to sequence
colouring.} and includes a javascript API to allow customisable display of
alignments for web sites such as Pfam.\footnote{\url{http://pfam.xfam.org}}


The Jalview Desktop in this version
provides access to protein and nucleic acid sequence, alignment and structure
databases, and includes the Jmol\footnote{ Provided under the LGPL licence at
\url{http://www.jmol.org}} viewer for molecular structures, and the VARNA\footnote{Provided under GPL licence at \url{http://varna.lri.fr}} program for the visualization of 
RNA secondary structure. It also
provides a graphical user interface for the multiple sequence alignment, conservation analysis 
and protein disorder prediction methods provided as {\bf Ja}va {\bf B}ioinformatics
{\bf A}nalysis {\bf W}eb {\bf S}ervices (JABAWS). JABAWS\footnote{released under GPL at \url{http://www.compbio.dundee.ac.uk/jabaws}} is a system for 
running bioinformatics programs that you can download and run on your own machine or cluster, or install on compute clouds.

\subsection{Jalview's Capabilities}
% TODO add references to appropriate sections for each capability described here.
Figure \ref{jvcapabilities} gives an overview of the main features of the
Jalview desktop application. Its primary function is the editing and
visualization of sequence alignments, and their interactive analysis. Tree
building, principal components analysis, physico-chemical property conservation
and sequence consensus analyses are built into the program. Web services enable
Jalview to access online alignment and secondary structure prediction programs,
as well as to retrieve protein and nucleic acid sequences, alignments, protein structures and sequence annotation. 
Sequences, alignments, trees, structures, features and alignment annotation may also be exchanged with the local filesystem. 
Multiple visualizations of an alignment may be worked on simultaneously, and the user interface provides a comprehensive set of controls for colouring and layout. 
Alignment views are dynamically linked with Jmol and UCSF Chimera\footnote{UCSF Chimera needs to be installed separately. It is available free for academic use from \url{https://www.cgl.ucsf.edu/chimera/download.html}.} structure displays,
a tree viewer and spatial cluster display, facilitating interactive exploration of the alignment's structure. The application provides its own Jalview project file format in order 
to store the current state of an alignment and analysis windows. Jalview also provides WYSIWIG\footnote{WYSIWIG: What You See Is What You Get.} style
 figure generation capabilities for the preparation of alignments for publication.
\begin{figure}[htbp]
\begin{center}
\includegraphics[width=5.8in]{images/jvcapabilities.pdf}
\caption{{\bf Capabilities of the Jalview Desktop.} The Jalview Desktop Application provides a stable environment for the creation, editing and analysis of alignments and the generation of figures.}
\label{jvcapabilities}
\end{center}
\end{figure}

\subsubsection{Jalview History}
Jalview was initially developed in 1996 by Michele Clamp, James Cuff, Steve
Searle and Geoff Barton at the University of Oxford and then the European
Bioinformatics Institute. Development of Jalview 2 was made possible with
eScience funding from the BBSRC\footnote{Biotechnology and Biological Sciences
Research Council grant  {\sl ``VAMSAS: Visualization and Analysis of Molecules,
Sequence Alignments and Structures"}, a joint project to enable interoperability
between Jalview, TOPALi and AstexViewer.} in 2004, enabling Andrew Waterhouse and
Jim Procter to re-engineer the original program to introduce contemporary developments
in bioinformatics and take advantage of the latest web and Java technology.
Jalview's development has been supported from 2009
onwards by BBSRC funding, and since 2014 by a
Wellcome Trust Biomedical Resource grant\footnote{Wellcome grant number 101651/Z/13/Z}. In 2010, 2011, and 2012, Jalview benefitted from the
\href{http://code.google.com/soc/}{Google Summer of Code}, when Lauren Lui and Jan Engelhardt introduced new features for handling RNA alignments and secondary structure annotation, in collaboration with Yann Ponty.\footnote{\url{http://www.lix.polytechnique.fr/~ponty/}}

 
%TODO describe future plans in history ? not a good idea.
% Jalview continues to be one of the worlds most popular\footnote{and in the authors opinion, the best.} sequence alignment and analysis tools.

\subsubsection{Citing Jalview}
If you use Jalview in your work you should cite:\newline
{\sl "Jalview Version 2 - a multiple sequence alignment editor and analysis
workbench"}\newline Waterhouse, A.M., Procter, J.B., Martin, D.M.A, Clamp, M. and Barton, G. J. (2009) \newline {\sl Bioinformatics}  doi: 10.1093/bioinformatics/btp033

This paper supersedes the original Jalview publication:\newline {\sl "The
Jalview Java alignment editor"} \newline Michele Clamp, James Cuff, Stephen M. Searle and Geoffrey J. Barton (2004) \newline {\sl Bioinformatics} {\bf 20} 426-427. 

  
\subsection{About this Tutorial }

This tutorial is written in a manual format with short exercises where
appropriate, typically at the end of each section. The first few sections concerns the
basic operation of Jalview and should be sufficient for those who want to
launch Jalview (Section \ref{startingjv}), open an alignment (Section
\ref{loadingseqs}), perform basic editing (Section
\ref{selectingandediting}), colouring (Section \ref{colours}), and produce
publication and presentation quality graphical output (Section \ref{layoutandoutput}).

The remaining sections of the manual cover the visualization and
analysis techniques available in Jalview. These include working
with the embedded Jmol molecular structure viewer (or UCSF Chimera), building
and viewing trees and Principal Components Analysis (PCA) plots, and using
trees for sequence conservation analysis. An overview of
the Jalview Desktop's webservices is given in Section \ref{jvwebservices}, and
the alignment and secondary structure prediction services are described
in detail in Sections \ref{msaservices} and \ref{protsspredservices}
respectively.
Section \ref{featannot} details the creation and visualization of sequence and alignment annotation. Section \ref{workingwithnuc} discusses
specific features of use when working with nucleic acid sequences, such as translation and linking to protein
coding regions, and the display and analysis of RNA secondary structure.

%^Chapter \ref{jalviewadvanced} The third chapter covers the detail^ of Jalview and is aimed at the user who is
%already familiar with Jalview operation but wants to get more out of their
%Jalview experience.

\subsubsection{Typographic Conventions}

Keystrokes using the special non-symbol keys are represented in the tutorial by
enclosing the pressed keys with square brackets ({\em e.g.} [RETURN] or [CTRL]).

Keystroke combinations are denoted with a `-' symbol ({\em
e.g.} [CTRL]-C means press [CTRL] and the `C' key simultaneously).

Menu options are given as a path from the menu
that contains them - for example {\sl File $\Rightarrow$ Input Alignment
$\Rightarrow$ From URL} means to select the `From URL' option from the `Input
Alignment' submenu of a window's `File' dropdown menu.

\section{Launching the Jalview Desktop Application}
\label{startingjv}
\begin{figure}[htbp]
\begin{center}
\includegraphics[width=4.5in]{images/download.pdf}
\caption{\bf Download page on the Jalview web site at www.jalview.org.}
\label{download}
\end{center}
\end{figure}

This tutorial is based on the Jalview
Desktop application. Much of the information will also be useful for users of
the JalviewLite applet, which has the same core editing, analysis and visualization capabilities (see the
\href{http://www.jalview.org/examples/applets.html}{JalviewLite Applet Examples}
page for examples). The Jalview Desktop, however, is much more powerful, and
includes additional support for interaction with external web services, and
production of publication quality graphics.

The Jalview Desktop can be run in two ways; as an application launched from the
web {\sl via} Java webstart, or as an application loaded onto your hard drive. 
The webstart version is launched from the pink `Launch Jalview Desktop
button' at the top right hand side of pages of the website 
\href{http://www.jalview.org}{(www.jalview.org)}.
To download the locally installable version, follow the links on the download
page
\href{http://www.jalview.org/download}{(www.jalview.org/download) }
 (Figure \ref{download}).
These links will launch the latest stable release of Jalview.\par

%% this paragraph needs to be rewritten for the new signed certificate from Certum.

When the application is launched with webstart, two dialogs may appear before
the application starts. If your browser is not set up to handle webstart, then
clicking the launch link may download a file that needs to be opened
manually, or prompt you to select the program to handle the webstart
file. If that is the case, then you will need to locate the {\bf javaws} program
on your system\footnote{The file that is downloaded will have a type of {\bf
application/x-java-jnlp-file} or {\bf .jnlp}. The {\bf javaws} program that can run
this file is usually found in the {\bf bin} directory of your Java
installation}. Once java webstart has been launched, you may also be prompted to
accept a security certificate signed by the Barton Group.\footnote{On some
systems, the certificate may be signed by 'UNKNOWN'. In this case, clicking
through the dialogs to look at the detailed information about the certificate
should reveal it to be a Barton group certificate.} You can always trust us, so
click trust or accept as appropriate. The splash screen (Figure \ref{splash})
gives information about the version and build date that you are running,
information about later versions (if available), and the paper to cite in your
publications. This information is also available on the Jalview web site at 
\url{http://www.jalview.org}.

%[fig 2] 
\begin{figure}[htbp]

\begin{center}
\includegraphics[width=4.5in]{images/splash.pdf}
\caption{{\bf Jalview splash screen.}}
\label{splash}
\end{center}
\end{figure}

When Jalview starts it will automatically load an example alignment from the
Jalview site. This behaviour can be switched off in the Jalview Desktop
preferences dialog  by unchecking the open file option.
This alignment will look like the one in Figure \ref{startpage} (taken
from Jalview version 2.10.1).

%[figure 3 ]
\begin{figure}[htbp]
\begin{center}
\includegraphics[width=4in]{images/start.pdf}
\caption{{\bf Default startup for Jalview.}}
\label{startpage}
\end{center}
\end{figure}


\subsubsection{Jalview News RSS Feed}

Announcements are made available to users of the
Jalview Desktop {\sl via} the Jalview Newsreader. This window will open
automatically when new news is available, and can also be accessed {\sl via} the
Desktop's {\sl Tools $\Rightarrow$ Show Jalview News} menu entry. 

\begin{figure}[htbp]
\begin{center}
\includegraphics[height=3in]{images/jvrssnews.pdf}
\caption{{\bf The Jalview News Reader.} The newsreader opens automatically
when new articles are available from the Jalview Desktop's news channel.}
\label{jalviewrssnews}
\end{center}
\end{figure}


\exercise{Launching Jalview from the Jalview Website}{
\label{start}
\exstep{Open the Jalview web site
\href{http://www.jalview.org}{(www.jalview.org)}
in your web browser. Launch Jalview by clicking on the
pink `Launch Jalview' Desktop button in the top right hand corner. This
will download and open a jalview.jnlp webstart file.}
\exstep {Dialog boxes
will open and ask if you want to open the jalview.jnlp file as the file is an application downloaded from the
Internet, click {\sl Open}. (Note you may be asked to update Java, if you agree
then it will automatically update the Java software). As Jalview opens, four demo
Jalview windows automatically load.}
\exstep {If
you are having trouble, it may help changing the browser you are using, as the browsers and
its version may affect this process.}
\exstep{To deactivate the opening of the 4 demo sequences during the launch, go
to the {\sl Tools $\Rightarrow$
Preferences...} menu on the desktop. A `Preference'
dialog box opens, untick the box adjacent to the `Open file' entry in the
`Visual' preferences tab.
Click {\sl OK} to save the preferences.}
\exstep{Launch another Jalview workbench from the web site by clicking on the
pink Launch button.
The example alignment should not be loaded as Jalview starts up.}
\exstep{To reload the original demo file select the
{\em File$\Rightarrow$ From URL} entry in the Desktop menu. Click on
the URL history button (a downward arrow on the right hand side of the dialog
box) to view the files, select exampleFile\_2\_7.jar, then click {\sl OK}.}
{\bf Note:} Should you want to load your own
sequence during the launch process, then go
to the {\sl Tools $\Rightarrow$
Preferences...} menu on the desktop. The tick the `Open file' entry of `Visual'
preferences tab, type in the URL of the sequence you want to load.


As the jalview.jnlp file launches Jalview on your desktop, you
may want to move this from the downloads folder to another folder.
Opening from the jnlp file will allow Jalview to be launched offline.

{\bf See the video at:
\url{http://www.jalview.org/Help/Getting-Started}.}
 }

\subsection{Getting Help}
\label{gettinghelp}
\subsubsection{Built in Documentation}
Jalview has comprehensive on-line help documentation. Select  {\sl Help
$\Rightarrow$ Documentation} from the main window menu and a new window will
open (Figure \ref{help}). The appropriate topic can then be selected from the
navigation panel on the left hand side. To search for a specific topic, click
the `search' tab and enter keywords in the box which appears.


\begin{figure}[htbp]
\begin{center}
\parbox[c]{2in}{\centerline{\includegraphics[width=2.75in]{images/help1.pdf}}}
\parbox[c]{4in}{\includegraphics[width=4in]{images/help2.pdf}}
\caption{{\bf Accessing the built in Jalview documentation.}}
\label{help}
\end{center}
\end{figure}

\subsubsection{Email Lists}

The Jalview Discussion list {\tt jalview-discuss@jalview.org} provides a forum
for Jalview users and developers to raise problems and exchange ideas - any
problems, bugs, and requests for help should be raised here. The {\tt
jalview-announce@jalview.org} list can also be subscribed to if you wish to be
kept informed of new releases and developments. 

Archives and mailing list
subscription details can be found in the Jalview web site's \href{http://www.jalview.org/community}{community section}.


\section{Navigation}
\label{jvnavigation}
The major features of the Jalview Desktop are illustrated in Figure \ref{anatomy}. The alignment window is the primary window for editing and visualization, and can contain several independent views of the alignment being worked with. The other windows (Trees, Structures, PCA plots, etc) are linked to a specific alignment view. Each area of the alignment window has a separate context menu accessed by clicking the right mouse button.  

 Jalview has two navigation and editing modes: {\bf normal mode}, where
 editing and navigation is performed using the mouse, and {\bf cursor mode}
 where editing and navigation are performed using the keyboard. The {\bf F2 key}
 is used to switch between these two modes. 
 
 {\em Note:} On MacBooks and other laptops with compact keyboards, you may need
 to press the {\bf function key [Fn]} when pressing any of the numbered function
 keys. So to toggle between keyboard and normal mode, press [Fn]-[F2].
 

\begin{figure}[htb]
\begin{center}
\includegraphics[width=6.5in]{images/jalview_anatomy.pdf}
\caption{{\bf The anatomy of Jalview.} The major features of the Jalview Desktop Application are labeled.}
% TODO: modify text labels to be clearer - black on grey and black border for clarity
\label{anatomy}
\end{center}
\end{figure}

\subsection{Navigation in Normal Mode}

Jalview always starts up in Normal mode, where the mouse is used to interact
with the displayed alignment view. You can move about the alignment by clicking
and dragging the ruler scroll bar to move horizontally, or by clicking and
dragging the alignment scroll bar to the right of the alignment to move
vertically.  If all the rows or columns in the alignment are displayed, the
scroll bars will not be visible.

 Each alignment view shown in the alignment window presents a window onto the
 visible regions of the alignment. This means that with anything more than a few
 residues or sequences, alignments can become difficult to visualize on the
 screen because only a small area can be shown at a time. It can help,
 especially when examining a large alignment, to have an overview of the whole
 alignment. Select {\sl View $\Rightarrow$ Overview Window} from the Alignment
 window menu bar (Figure \ref{overview}\footnote{the menu shown in this figure
 is from Jalview 2.2, later versions have more options.}).
% (Figure4)
\begin{figure}[htbp]
\begin{center}
\includegraphics[width=4.5in]{images/overview.pdf}
\caption{{\bf Alignment Overview Window.} The overview window for a view is opened from the {\em View} menu.}
\label{overview}
\end{center}
\end{figure}

The red box in the overview window shows the current view in the alignment
window. A percent identity histogram is plotted below the alignment overview.
Shaded parts indicate rows and columns of the alignment that are hidden (in this
case, a single row at the bottom of the alignment - see Section
\ref{hidingregions}). You can navigate around the alignment by dragging the red
box. 

%Try this now and see how the view in the alignment window changes.

\parbox[c]{3in}{Alignment and analysis windows are closed by clicking on the
usual `close' icon (indicated by arrows on Mac OS X). If you want to close all
the alignments and analysis windows at once, then use the {\sl Window
$\Rightarrow$ Close All} option from the Jalview desktop.

{\bf \em{Warning: Make sure you have saved your work because this cannot be
undone!}} }
\parbox[c]{3in}{\centerline{\includegraphics[width=2.5in]{images/start_closeall.pdf}
}}

\subsection{Navigation in Cursor Mode}
\label{cursormode}
\parbox[c]{5in}{Cursor mode navigation enables the user to quickly
and precisely navigate, select and edit parts of an alignment. On pressing F2 to
enter cursor mode the position of the cursor is indicated by a black background
and white text. The cursor can be placed using the mouse or moved by pressing
the arrow keys ($\uparrow$, $\downarrow$, $\leftarrow$, $\rightarrow$).
}\parbox[c]{1.25in}{\centerline{\includegraphics[width=0.8in]{images/cursor1.pdf}}}

Rapid movement to specific positions is accomplished as listed below:
\begin{list}{$\circ$}{}
\item {\bf Jump to Sequence {\sl n}:} Type a number {\sl n} then press [S] to
move to sequence (row) {\sl n}.
\item {\bf Jump to Column {\sl n}:} Type a number {\sl n} then press [C] to move to column {\sl n} in the alignment.  
\item {\bf Jump to Residue {\sl n}:} Type a number {\sl n} then press [P] to move to residue number {\sl n} in the current sequence.  
\item {\bf Jump to  column {\sl m} row {\sl n}:} Type the column number {\sl m}, a comma, the row number {\sl n} and press [RETURN]. 
\end{list}
\subsection{The Find Dialog Box}
\label{searchfunction}
A further option for navigation is to use the {\sl Select $\Rightarrow$
Find\ldots} function. This opens a dialog box into which can be entered regular
expressions for searching sequences and sequence IDs, or sequence numbers.
Hitting the [Find next] button will highlight the first (or next) occurrence of
that pattern in the sequence ID panel or the alignment, and will adjust the view
in order to display the highlighted region. The Jalview Help provides
comprehensive documentation for this function, and a quick guide to the regular
expressions that can be used with it.
%TODO insert a figure for the Find dialog box

\exercise{Navigation}{
Jalview has two navigation and editing modes: {\bf normal} mode (where editing
and navigation are via the mouse) and the {\bf cursor} mode (where editing and
navigation are via the keyboard).
The {\bf F2 key} is used to switch between these two modes. With a Mac, the key
combination {\bf Fn key and F2} is needed, as button is
often assigned to screen brightness. Jalview always starts up in normal mode.

\exstep{Load an example alignment from its URL
(\url{http://www.jalview.org/examples/exampleFile_2_7.jar}) via the Desktop
using {\sl File $\Rightarrow$ Input Alignment $\Rightarrow$ From URL} dialog
box.
(The URL should be stored in its history and clicking on the {\sl down arrow}
on the dialog box is an easy way to access it.)}
\exstep{Scroll around the alignment using the alignment (vertical) and ruler (horizontal) scroll bars.}
\exstep{Find the Overview Window, {\sl Views
$\Rightarrow$ Overview Window} and open it. Move around the
alignment by clicking and dragging the red box in the overview window.}
\exstep{Return to the alignment window, look at the status bar (lower left
hand corner of the alignment window) as you move the mouse over the alignment. It indicates information about the
sequence and residue under the cursor.}
\exstep{Press [F2] key, or [Fn]-[F2] on Mac, to enter Cursor mode. Use
the direction keys to move the cursor around the alignment.}
\exstep{Move to sequence 7 by pressing {\bf 7 S}. Move to column 18 by pressing
{\bf 1 8 C}. Move to residue 18 by pressing {\bf 1 8 P}. Note that these can be
two different positions if gaps are inserted into the sequence. Move to sequence 5,
column 13 by typing {\bf 1 3 , 5} [RETURN].}

{\bf Note:} To view Jalview's comprehensive on-line help documentations select
{\sl Help} in desktop menu, clicking on {\sl Documentation} will open a
Documentation window. Select topic from the navigation panel on the left hand side or use the
Search tab to select specific key words.

{\sl\bf See the video at: 
\url{http://www.jalview.org/Help/Getting-Started}.}
}

\section{Loading Sequences and Alignments}
\label{loadingseqs}
%Jalview provides many ways to load your own sequences. %For this section of the
% tutorial you will need to download the file http://www.jalview.org/tutorial/alignment.fa to a suitable location on your hard drive.
\subsection{Drag and Drop}
        In most operating systems you can just drag a file icon from a file browser
        window and drop it on an open Jalview application window. The file will then be opened as a new alignment window. %You can try this with the tutorial file you have downloaded. When you have opened the file, close it again by selecting the close control on the window. If you drop an alignment file onto an open alignment window it will be appended.
        Drag and drop also works when loading data from a URL -
simply drag the link or url from the address panel of your browser on to an
alignment or the Jalview desktop background and Jalview will load data from the
URL directly.
%  (Figure \ref{drag})
% %[fig 5]
% \begin{figure}[htbp]
% \begin{center}
% \includegraphics[width=2in]{images/drag2.pdf}
% \includegraphics[width=2in]{images/drag3.pdf}
% \caption{{\bf An alignment can be opened by dragging the file onto the Jalview window. }}
% \label{drag}
% \end{center}
% \end{figure}
% 
% %\includegraphics[width=2in]{images/drag1.pdf}


\subsection{From a File}
Jalview can read sequence alignments from a sequence alignment file. This is a
text file, {\bf not} a word processor document. For entering sequences from a
wordprocessor document see Cut and Paste  (Section \ref{cutpaste}) below. Select
{\sl File $\Rightarrow$ Input Alignment $\Rightarrow$ From File} from the main
menu (Figure \ref{loadfile}). You will then get a file selection window where
you can choose the file to open. Remember to select the appropriate file type.
Jalview can automatically identify some sequence file formats.

%[fig 6]
\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2in]{images/loadfilebox.pdf}
%\includegraphics[width=2in]{images/loadfilebox2.pdf}
\includegraphics[width=3in]{images/loadfileboxdrop.pdf}
\caption{{\bf Opening an alignment from a file saved on disk. }}
\label{loadfile}
\end{center}
\end{figure}

\subsection{From a URL}
Jalview can read sequence alignments directly from a URL. Please note that the
files must be in a sequence alignment format - an HTML alignment or graphics
file cannot be read by Jalview.
Select {\sl File $\Rightarrow$ Input Alignment $\Rightarrow$ From URL} from the
main menu and a window will appear asking you to enter the URL (Figure
\ref{loadurl}). Jalview will attempt to automatically discover the file format.

%[fig 7]
\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2in]{images/menuloadurl.pdf}
\includegraphics[width=3in]{images/loadurlbox.pdf}
\caption{{\bf Opening an alignment from a URL. }}
\label{loadurl}
\end{center}
\end{figure}

\subsection{Cut and Paste}
\label{cutpaste}
Documents such as those produced by Microsoft Word cannot be readily understood
by Jalview. The way to read sequences from these documents is to select the
data from the document and copy it to the clipboard. There are two ways to
do this. One is to right-click on the desktop background, and select the
`Paste to new window' option in the menu that appears. The other is to select
{\sl File $\Rightarrow$ Input Alignment $\Rightarrow$ From Textbox} from the
main menu, paste the sequences into the text window that will appear, and select
{\sl New Window} (Figure \ref{loadtext}). In both cases, presuming that they are
in the right format, Jalview will happily read them into a new alignment window.
%[fig 8]

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2in]{images/menuloadtext.pdf}
\includegraphics[width=3in]{images/loadtextbox.pdf}
\caption{{\bf Opening an alignment from pasted text. }}
\label{loadtext}
\end{center}
\end{figure}


\subsection{From a Public Database}
\label{fetchseq}
Jalview can retrieve sequences and sequence alignments from the public databases
housed at the European Bioinformatics Institute, including Uniprot, Pfam, Rfam
and the PDB. Jalview's sequence fetching capabilities allow you to avoid having to
manually locate and save sequences from a web page before loading them into
Jalview. It also allows Jalview to gather additional metadata provided by the
source, such as annotation and database cross-references.
Select {\sl File $\Rightarrow$ Fetch Sequence(s) \ldots} from the main menu and
a window will appear (Figure \ref{loadseq}). Pressing the database selection
button in the dialog box opens a new window showing all the database sources
Jalview can access (grouped by the type of database). Once you've selected the
appropriate database, hit OK close the database selection window, and then enter
one or several database IDs or accession numbers separated by a semicolon and
press OK. Jalview will then attempt to retrieve them from the chosen database.
Example queries are provided for some databases to test that a source is
operational, and can also be used as a guide for the type of accession numbers
understood by the source.
% [fig 9]
\begin{figure}[htbp]
\begin{center}
\includegraphics[width=5in]{images/fetchseq.pdf}
\caption{{\bf Retrieving sequences from a public database.}}
\label{loadseq}
\end{center}
\end{figure}
 
\subsection{Memory Limits}
\label{memorylimits}
Jalview is a Java program. One unfortunate implication of this is that Jalview
cannot dynamically request additional memory from the operating system. It is
important, therefore, that you ensure that you have allocated enough memory to
work with your data. On most occasions, Jalview will warn you when you have
tried to load an alignment that is too big to fit in to memory (for instance,
some of the PFAM alignments are {\bf very} large). You can find out how much
memory is available to Jalview with the desktop window's {\sl $\Rightarrow$
Tools $\Rightarrow$ Show Memory Usage} function, which enables the display of
the currently available memory at the bottom left hand side of the Desktop
window's background. Should you need to increase the amount of memory available
to Jalview, full instructions are given in the built in documentation (opened by
selecting {\sl Help $\Rightarrow$ Documentation}) and on the JVM memory
parameters page (\url{http://www.jalview.org/jvmmemoryparams.html}).

\exercise{Loading Sequences}{
\label{load}
\exstep{Use {\sl Window $\Rightarrow$ Close All} from the Desktop window menu to
close all windows.}
\exstep{{\bf Loading sequences from URL:} Selecting File {\sl $\Rightarrow$
Input Alignment $\Rightarrow$ From URL} from the Desktop and enter \textsf{http://www.jalview.org/tutorial/alignment.fa} in the box.

Click {\sl OK} to load the alignment.}
\exstep{{\bf Loading sequences from a file:} Close all windows using the
{\sl Window $\Rightarrow$ Close All} menu option from the Desktop.
Then type the same URL (\url{http://www.jalview.org/tutorial/alignment.fa}) into
your web browser and save the file to your desktop.
Open the file you have just saved in Jalview by selecting {\sl File
$\Rightarrow$ Input Alignment $\Rightarrow$ From File} from the desktop menu and
selecting this file.
Click {\sl OK} to load.}
\exstep{{\bf Loading sequences by `Drag and Drop' / `Cut and Paste':}

(i) Select {\sl Desktop $\Rightarrow$ Window
$\Rightarrow$ Close All}. Then drag the alignment.fa file from the desktop and
drop it onto the Jalview window, the alignment should open.

(ii) Test the differences
between (a) dragging the sequence onto the Jalview desktop  and (b)
dragging the sequence onto an existing alignment window.

(iii) Open \url{http://www.jalview.org/tutorial/alignment.fa} in a
web browser. Drag the URL directly from browser onto Jalview desktop. (If
the URL is downloaded, then locate the file in your
download directory and open it in a text editor.)}

\exstep{{\bf The text editor:} (i) Open the alignment.fa file using text editor.
Copy the sequence text from the file into the clipboard and paste it into the desktop
background by right-clicking and selecting the {\sl Paste to New Window} menu
option.

(ii) In the text editor, copy the sequence text from
alignment.fa  into the clipboard (usually {\sl via} the browser's {\sl Edit
$\Rightarrow$ Copy} menu option). 

(iii) In the Desktop menu, select {\sl File
$\Rightarrow$ Input Alignment $\Rightarrow$ From Textbox}.
Paste the clipboard into the large window using the {\sl Edit $\Rightarrow$
Paste} text box menu option. Click {\sl New Window} and the alignment will be
loaded.}

\exstep{{\bf Loading sequences from Public Database:} (i) Select {\sl File
$\Rightarrow$ Fetch Sequence(s)...} from the Desktop. The {\sl Select Database
Retrieval Source} dialog will open showing all the database sources. Select the
{\bf PFAM seed} database and click {\sl OK}.

(ii)Once a source has been selected, the {\sl New
Sequence Fetcher} window will open. Enter the accession number {\bf PF03460}
and click {\sl OK}.
An alignment of about 174 sequences should load.}
\exstep{These can be viewed using the Overview window accessible from {\sl View
$\Rightarrow$ Overview Window.}
Several database IDs can be loaded by using semicolons to separate them.}
{\bf See the video at:
\url{http://www.jalview.org/Help/Getting-Started}} }

\section{Saving Sequences and Alignments}
\label{savingalignments} 
\subsection{Saving Alignments} Jalview allows alignments to be saved to file
in a variety of formats so they can be restored at a later date, passed to
colleagues or analysed in other programs. From the alignment window menu select {\sl File $\Rightarrow$ Save As} and a dialog box
will appear (Figure \ref{savealign}). You can navigate to an appropriate
directory in which to save the alignment. Jalview will remember the last filename
and format used to save (or load) the alignment, enabling you to quickly save
the file during or after editing by using the {\sl File $\Rightarrow$ Save}
entry. The {\sl File $\Rightarrow$ Output To Textbox} menu option allows the alignment to be copied and pasted into
other documents or web servers.

Jalview offers several different formats in which an alignment can be saved.
Of these, only the jalview project format (.jar or .jvp) will preserve the colours, groupings and other additional information in the alignment. The other formats
produce text files containing just the sequences with no visualization information, although some
allow limited annotation and sequence features to be stored (e.g. AMSA).
Unfortunately, as far as we are aware only Jalview can read Jalview
project files.

%[fig 10]
\begin{figure}[htbp]
\begin{center}
\parbox[c]{1.0in}{
\includegraphics[width=1.0in]{images/saveas.pdf}
}
\parbox[c]{4in}{
\includegraphics[width=4in]{images/saveas2.pdf}
}
\caption{{\bf Saving alignments in Jalview to disk.}}
\label{savealign}
\end{center}
\end{figure}

\subsection{Jalview Projects}
\parbox[c]{4in}{If you wish to save a complete Jalview session rather than
just a single alignment (e.g. because you have calculated trees or multiple
different alignments) then save your work as a Jalview Project
file (.jvp).\footnote{Tip: Ensure that you have allocated plenty of memory to
Jalview when working with large alignments in Jalview projects. See Section 
\ref{memorylimits} for how to do this.}
From the main menu select {\sl File $\Rightarrow$ Save Project} and a file save
dialog box will appear. Loading a project will restore Jalview to exactly the
view at which the file was saved, complete with all alignments, trees,
annotation and displayed structures rendered appropriately.
} \parbox[c]{2in}{ \centerline {
\includegraphics[width=1.5in]{images/saveproj.pdf} }}

\exercise{Saving Alignments}{
\label{save}
\exstep{Launch Jalview afresh, or use {\sl Desktop $\Rightarrow$ Window
$\Rightarrow$ Close all }.}
\exstep{Load the ferredoxin
alignment ({\bf PF03460}) from {\bf PFAM (seed)} (see Exercise
\ref{load}).
} \exstep{

Select {\sl File $\Rightarrow$ Save As} from the alignment window menu. Choose a
location into which to save the alignment and select your preferred format. All
formats except {\sl  Jalview } jvp can be viewed in a normal text editor (e.g.
Notepad) or in a web browser.
Enter a file name and click {\sl Save}.}
\exstep{Check this file by closing all windows and opening it with Jalview, or by
browsing to it with your web browser.}
\exstep{Repeat the previous steps saving the files in different file formats.}
\exstep{Select {\sl File $\Rightarrow$ Output to Textbox $\Rightarrow$ FASTA}.
Select and copy this alignment to the clipboard using the textbox menu options
{\sl Edit $\Rightarrow$ Select All} followed by {\sl Edit $\Rightarrow$ Copy}.
The alignment can then be pasted into any application of choice, e.g. a word processor or web form.
}
\exstep{Ensure at least one alignment window is active in Jalview. Open the
overview window {\sl View $\Rightarrow$ Overview Window}
 and scroll red box to any part of the alignment.
Select {\sl File
$\Rightarrow$ Save Project} from the main menu and save the project in a
suitable folder.}

\exstep{Close all windows and then load the project {\sl via} the {\sl File
$\Rightarrow$ Load Project} menu option. Observe how all the windows and
positions are exactly as they were when they were saved. } 
{\bf See the video at: \url{http://www.jalview.org/Help/Getting-Started}.}
}


\chapter{Selecting and Editing Sequences }
\label{jalviewediting}

\label{selectingandediting} 
Jalview makes extensive use of selections - most of the commands available from
its menus operate on the {\sl currently selected region} of the alignment, either to
change their appearance or perform some kind of analysis. This section
illustrates how to make and use selections and groups.

\section{Selecting Parts of an Alignment}
Selections can be of arbitrary regions in an alignment, one or more complete columns, or one or 
more complete sequences.
A selected region can be copied and pasted as a new alignment 
using the {\sl Edit $\Rightarrow$ Copy} and {\sl Edit $\Rightarrow$ Paste $\Rightarrow$ To New 
Alignment}  in the alignment window menu options.
{\bf To clear (unselect)  the selection press the [ESC] (escape) key.}

\subsection{Selecting Arbitrary Regions}
To select part of an alignment, place the mouse at the top left corner of the region you wish to select. Press and hold the mouse button and drag the mouse to the bottom right corner of the chosen region then release the mouse button. 
A dashed red box appears around the selected region (Figure \ref{select}). 
%[fig 12]

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=4in]{images/select1.pdf}
\caption{{\bf Selecting a region in an alignment.}}
\label{select}
\end{center}
\end{figure}

\subsection{Selecting Columns}
To select the same residues in all sequences, click and drag along the alignment ruler.
This selects the entire column of the alignment. Ranges of positions from the
alignment ruler can also be selected by clicking on the first position and then
holding down the [SHIFT] key whilst clicking the other end of the selection.
Discontinuous regions can be selected by holding down [CTRL] and clicking on
positions to add to the column selection. Note that each [CTRL]-Click (PC) or
[CMD]-Click (Mac) changes the current selected sequence region to that column,
but adds to the column selection.
Selected columns are indicated by red highlighting in the ruler bar (Figure \ref{selectcols}).
%[fig 13]

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=4in]{images/select2.pdf}
\caption{{\bf Selecting multiple columns in an alignment.} The red highlighting
on the alignment ruler marks the selected columns. Note that only the most
recently selected column has a dashed-box around it to indicate a region
selection. }
\label{selectcols}
\end{center}
\end{figure}

\subsection{Selecting Sequences}

\begin{figure}[htb]
\begin{center}
\includegraphics[width=4in]{images/select3.pdf}
\caption{{\bf Selecting multiple sequences in an alignment.} Use [CTRL] or [SHIFT] to select many sequences at once.}
\label{selectrows}
\end{center}
\end{figure}

To select multiple complete sequences, click and drag the mouse down the
sequence ID panel. The same techniques as used for columns (above) can be used
with [SHIFT]-Click for continuous and [CTRL]-Click to select discontinuous
ranges of sequences (Figure \ref{selectrows}).
%[fig 14]

\subsection{Making Selections in Cursor Mode}

To define a selection in cursor mode (which is enabled by pressing [F2] when the alignment window is selected),
navigate to the top left corner of the proposed selection (using the mouse, the arrow keys, or the keystroke
commands described in Section \ref{cursormode}). Pressing the [Q] key marks this as the
corner. A red outline appears around the cursor (Figure \ref{cselect}).

Navigate to the bottom right corner of the proposed selection and press the [M] key. This marks the bottom right corner of the selection. The selection can then be treated in the same way as if it had been created in normal mode.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=1.5in]{images/csel1.pdf}
\includegraphics[width=1.5in]{images/csel2.pdf}
\includegraphics[width=1.5in]{images/csel3.pdf}
\includegraphics[width=1.5in]{images/csel4.pdf}
\caption{{\bf Making a selection in cursor mode.} Navigate to the top left
corner (left), press [Q], navigate to the bottom right corner and press [M] (right).}
\label{cselect}
\end{center}
\end{figure}

\begin{figure}
\begin{center}
\includegraphics[width=3in]{images/group1.pdf}
\includegraphics[width=1.5in]{images/newgroup.pdf}
\caption{{\bf Creating a new group from a selection.}}
\label{makegroup}
\end{center}
\end{figure}

\subsection{Inverting the Current Selection}
The current sequence or column selection can be inverted, using  {\sl Select
$\Rightarrow$ Invert Sequence/Column Selection} in the alignment window.
Inverting the selection is useful when selecting large regions in an alignment, 
simply select the region that is to be kept unselected, and then invert the selection.
This may also be useful when hiding large regions in an alignment (see Section \ref{hidingregions} 
below).
Instead of selecting the columns and rows that are to be hidden, simply select the 
region that is to be kept
visible, invert the selection, then select {\sl View $\Rightarrow$ Hide
$\Rightarrow$ Selected Region}.

\section{Creating Groups}
Selections are lost as soon as a different region is selected. Groups can be
created which are labeled regions of the alignment. To create a group, first
select the region which is to comprise the group. Then click the right mouse
button on the selection to bring up a context menu. Select {\sl Selection
$\Rightarrow$ Group $\Rightarrow$ Edit name and description of
current group}\footnote{In earlier versions of Jalview, this entry was variously
`Group', `Edit Group Name', or `JGroupXXXXX' (Where XXXXX was some serial
number).} then enter a name for the group in the dialog box which appears.

By default the new group will have a box drawn around it. The appearance of the group can be changed (see Section \ref{colours} below). This group will stay defined even when the selection is removed.

\exercise{Making Selections and Groups}{
\label{exselect}
\exstep{Close windows.

Load the ferredoxin alignment ({\bf PF03460} from {\bf PFAM (seed)}).
}
\exstep{Selecting an arbitrary region. Choose a residue and place the mouse
cursor on it (residue information will show in alignment window status
bar).
Click and drag the mouse to the bottom-right to create a selection. As you drag,
a red box will `rubber band' out to 
show the extent of the selection.
Release the mouse
button and a red box borders the selected region.
Press [ESC] to clear this.}
\exstep{ Select one sequence by clicking on
the sequence ID panel. Note that the sequence ID takes on a highlighted
background and a red box appears around the selected sequence. 
Hold down [SHIFT] and click another sequence ID a few positions above or below. 
Note how the selection expands to include all the sequences between the two positions on which you clicked.
Hold down [CTRL] and then click on several sequences' IDs - both selected and
unselected. Note how unselected IDs are individually added to the selection and previously selected IDs are 
individually deselected.}
\exstep{ Select columns by clicking on the Alignment Ruler. Note
that the selected column is marked with a red box.
Hold down [SHIFT] and click a column beyond. Note the selection expands to
include all the sequences between the two positions on which you clicked.}

\exstep{Enter Cursor mode using [F2], or [Fn]-F2 for Macs.
Navigate to column 59, row 1 by pressing {\bf 5 9 , 1 [RETURN]}.
Press {\bf Q} to mark this position.
Navigate to column 65, row 8 by pressing {\bf 6 5 , 8 [RETURN]}. Press {\bf M}
to complete the selection. Note to clear the selection press the [ESC]
key.}
\exstep{To create a group from the selected the region, click the
right mouse button when mouse is on the selection, this opens a
context menu in the alignment window.

Open the {\sl Selection $\Rightarrow$ Edit New Group $\Rightarrow$ Group Colour
} menu and select {\sl Percentage Identity}.
This will turn the selected region into a group and colour it accordingly.}
\exstep{Hold down [CTRL] and use the mouse to select and deselect sequences in
the alignment by clicking on their Sequence ID label. Note how the group expands
to include newly selected sequences, and the Percentage Identity colouring changes. }
\exstep{ Another way to resize the group is by using the mouse to click and drag
the right-hand edge of the selected group.}

\exstep{The current selection can be exported and saved by right clicking the
mouse when on the text area to open the Sequence ID context menu. Follow the
menus and pick an output format (eg BLC) from the {\sl Selection $\Rightarrow$ Output to Textbox
\ldots} submenu.
}
\exstep{In the Alignment output window that opens, try manually editing the
alignment before clicking the {\sl New Window} button. This opens the
edited alignment in a new alignment window.} {\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
% more? change colouring style. set border colour.
}

\section{Exporting the Current Selection}
The current selection can be copied to the clipboard (in PFAM format). It can
also be output to a textbox using the output functions in the pop-up menu
obtained by right clicking the current selection. The textbox enables quick
manual editing of the alignment prior to importing it into a new window (using
the {\sl New Window} button) or saving to a file with the {\sl File
$\Rightarrow$ Save As } pulldown menu option from the text box.

\section{Reordering an Alignment}
Sequence reordering is simple. Highlight the sequences to be moved then press the up or down arrow keys as appropriate (Figure \ref{reorder}). If you wish to move a sequence up past several other sequences it is often quicker to select the group past which you want to move it and then move the group rather than the individual sequence.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=3in]{images/move1.pdf}
\includegraphics[width=3in]{images/move2.pdf}
\caption{{\bf Reordering the alignment.} The selected sequence moves up one
position on pressing the $\uparrow$ key.}
\label{reorder}
\end{center}
\end{figure}

\exercise{Reordering the Alignment}{
\exstep{Close windows.

Load the ferredoxin alignment ({\bf PF03460} from {\bf PFAM (seed)}).
}
\exstep{Select one of the sequence in the sequence ID panel, use the up and down
arrow keys to alter the sequence's position in the alignment. (Note that
this will not work in cursor mode)}
\exstep{To select and move multiple
sequences, use hold [SHIFT], and select two sequences separated by
one or more un-selected sequences, repeat using the [CTRL] key. Note how
multiple sequences are grouped together when they are re-ordered using the up and down arrow keys.}
{\bf See the video at: \url{http://www.jalview.org/training/Training-Videos}.}
}


\section{Hiding Regions}
\label{hidingregions}
It is sometimes convenient to exclude some sequences or residues in the alignment without actually deleting them. Jalview allows sequences or alignment columns within a view to be hidden, and this facility has been used to create the several different views in the example alignment file that is loaded when Jalview is first started (See Figure \ref{startpage}).

To hide a set of sequences, select them and right-click the mouse on the
selected sequence IDs to bring up the context pop-up menu. Select {\sl Hide
Sequences} and the sequences will be concealed, with a small blue triangle indicating their position (Figure \ref{hideseq}). To unhide (reveal) the sequences, right click on the triangle and select {\sl Reveal Sequences} from the context menu.


 \begin{figure}[htbp]
\begin{center}
\includegraphics[width=1.5in]{images/hide1.pdf}
\includegraphics[width=2.5in]{images/hide2.pdf}
\includegraphics[width=1.75in]{images/hide3.pdf}
\caption{{\bf Hiding Sequences} Hidden sequences are represented by a small blue
triangle in the sequence ID panel.}
\label{hideseq}
\end{center}
\end{figure}

A similar mechanism applies to columns (Figure \ref{hidecol}). Selected columns
(indicated by a red marker) can be hidden and revealed in the same way {\sl via}
the context pop-up menu by right clicking on the ruler bar. The hidden column
selection is indicated by a small blue triangle in the ruler bar.

 \begin{figure}[htbp]
\begin{center}
\includegraphics[width=2in]{images/hide4.pdf}
\includegraphics[width=3in]{images/hide5.pdf}
\includegraphics[width=1in]{images/hide6.pdf}
\caption{{\bf Hiding Columns} Hidden columns are represented by a small blue
triangle in the ruler bar.}
\label{hidecol}
\end{center}
\end{figure}

It is often easier to select the region that you intend to work with, rather
than the regions that you want to hide. In this case, select the required region and use the {\sl View $\Rightarrow$ Hide
$\Rightarrow$ All but Selected Region } menu entry, or press [Shift]+[Ctrl]+H
to hide the unselected region.

\subsection{Representing a Group with a Single Sequence}

Instead of hiding a group completely, it is sometimes useful to work with just one representative sequence. The {\sl $<$Sequence ID$>$ $\Rightarrow$ Represent group with $<$Sequence ID$>$ } option from the sequence ID pop-up menu enables this variant of the hidden groups function. The remaining representative sequence can be visualized and manipulated like any other. However, any alignment edits that affect the sequence will also affect the whole sequence group. 

\exercise{Hiding and Revealing Regions}{
\exstep{Close windows.

Load the ferredoxin alignment ({\bf PF03460} from {\bf PFAM (seed)}).
}
\exstep{Select a contiguous set of sequences by clicking and dragging on the sequence ID panel.
Right click on the selected sequence IDs to bring up the sequence ID context
menu, select {\sl Hide Sequences}.
}
\exstep{
Right click on the blue triangle indicating hidden sequences and select {\sl
Reveal Sequences} in the panel. (If you have hidden all sequences then you will
need to use the alignment window menu option {\sl View $\Rightarrow$ Show $\Rightarrow$ 
All Sequences.}) }
\exstep{
Repeat the process but use a non-contiguous set of sequences. Note that when
multiple regions are hidden you can select either {\sl
Reveal Sequences} to reveal the hidden sequences that were clicked, or {\sl
Reveal All}.
}
\exstep{Repeat the above using columns to hide and reveal columns
instead of sequences.}
\exstep{Select a region of the alignment, and experiment with the {\sl Hide all
but selected region} option in {\sl View $\Rightarrow$ Hide $\Rightarrow$ All
but selected region.}} \exstep{Select some sequences, pick one to represent the rest by hovering
the mouse over this sequence. Bring up the Sequence ID context menu by right
clicking and select {\sl (Sequence ID name) $\Rightarrow$ Represent group
with (Sequence ID name )}. To reveal these hidden sequences, right click on the
Sequence ID and in the context menu select {\sl Reveal All}.}
{\bf See the video at:  \url{http://www.jalview.org/training/Training-Videos}.}
}


\begin{figure}[htb]
\begin{center}
\includegraphics[width=3in]{images/edit1.pdf}
\includegraphics[width=3in]{images/edit2.pdf}
\caption{{\bf Introducing gaps in a single sequence.} Gaps are introduced as the
selected sequence is dragged to the right while pressing and holding [SHIFT].}
\label{gapseq}
\end{center}
\end{figure}

\begin{figure}[htb]
\begin{center}
\includegraphics[width=3in]{images/edit3.pdf}
\includegraphics[width=3in]{images/edit4.pdf}
\caption{{\bf Introducing gaps in a group.} Gaps are introduced as the selected
group is dragged to the right with [CTRL] pressed.}
\label{gapgroup}
\end{center}
\end{figure}

\section{Introducing and Removing Gaps}
The alignment view provides an interactive editing interface, allowing gaps to be inserted or deleted to the left of any position in a sequence or sequence group. Alignment editing can only be performed whilst in keyboard editing mode (entered by pressing [F2]) or by clicking and dragging residues with the mouse when [SHIFT] or [CTRL] is held down (which differs from earlier versions of Jalview).


\subsection{Undoing Edits}
Alignment edits can be undone {\sl via} the {\sl Edit $\Rightarrow$ Undo Edit}
alignment window menu option, or CTRL-Z. An edit, if undone, may be re-applied
with {\sl Edit $\Rightarrow$ Redo Edit}, or CTRL-Y. Note, however, that the
{\sl Undo} function only works for edits to the alignment or sequence ordering.
Colouring of the alignment, showing and hiding of sequences or modification of
annotation that only affect the alignment's display cannot
be undone.

\subsection{Locked Editing}
\label{lockededits}
The Jalview alignment editing model is different to that used in other alignment
editors. Because edits are restricted to the insertion and deletion of gaps to the left of a particular sequence position, 
editing has the effect of shifting the rest of the sequence(s) being edited down or up-stream with respect to the rest of 
alignment. The {\sl Edit $\Rightarrow$ Pad Gaps} option can be enabled to eliminate `ragged edges' at the end of the alignment, 
but does not avoid the `knock-on' effect which is sometimes undesirable. 
However, its effect can be limited by performing the edit within a selected region. 
In this case, gaps will only be removed or inserted within the selected region. 
Edits are similarly constrained when they occur adjacent to a hidden column.

\subsection{Introducing Gaps in a Single Sequence}
To introduce a gap, first select the sequence in the sequence ID panel and
then place the cursor on the residue to the immediate right of where the gap
should appear. Hold down the SHIFT key and the left mouse button, then drag the sequence to the right until the required number of gaps has been inserted.

One common error is to forget to hold down [SHIFT]. This results in a selection which is one sequence high and one residue long. Gaps cannot be inserted in such a selection. The selection can be cleared and editing enabled by pressing the [ESC] key.

\subsection{Introducing Gaps in all Sequences of a Group}
To insert gaps in all sequences in a selection or group, select the
required sequences in the sequence ID panel and then place the mouse cursor on
any residue in the selection or group to the immediate right of the position in which a gap should appear. Hold down the CTRL key and the left mouse button, then drag the sequences to the right until the required number of gaps has appeared.

Gaps can be removed by dragging the residue to the immediate right of the gap
leftwards whilst holding down [SHIFT] (for single sequences) or [CTRL] (for a group of sequences).

\newpage

\exercise{Editing Alignments}
  %\label{mousealedit}
% TODO: VERIFY FOR 2.6.1 and 2.7 - NUMBERING/INSTRUCTIONS APPEAR OFF
{You are going to manually reconstruct part of the example Jalview
alignment available at
 \href{http://www.jalview.org/examples/exampleFile.jar}
 {http://www.jalview.org/examples/exampleFile.jar}.

{\sl {\bf Mac Users:} Please use the Apple or [CMD] key in place of [CTRL]
for key combinations such as [CTRL]-A. }

Remember to use [CTRL]-Z to undo an edit, or the {\sl File $\Rightarrow$
 Reload } function to revert the alignment back to the original version if you
 want to start again.

\exstep{ Load the URL
\textsf{http://www.jalview.org/tutorial/unaligned.fa} which contains part of the
ferredoxin alignment from PF03460.}

\exstep{ Select the first 7 sequences, and press H to hide them (or right click
on the sequence IDs to open the sequence ID context menu, and select {\sl Hide
Sequences}).}

\exstep{ Select FER3\_RAPSA and FER\_BRANA. Slide the sequences to
the right so the initial residue A lies at column 57 using the $\Rightarrow$
key.}

\exstep{ Select FER1\_SPIOL, FER1\_ARATH, FER2\_ARATH, Q93Z60\_ARATH and
O80429\_MAIZE

{\sl Hint: you can do this by pressing [CTRL]-I to invert the sequence selection and then
deselect FER1\_MAIZE), and use the $\Rightarrow$ key to slide them to so they
begin at column 5 of the alignment view.}} 

\exstep{ Select all the visible
sequences (those not hidden) in the block by pressing [CTRL]-A.
Insert a single
gap in all selected sequences at column 38 of the alignment by holding [CTRL]
and clicking on the R at column 38 in the FER1\_SPIOL, then drag one
column to right.
Insert another gap at column 47 in all sequences in the same way.}

\exstep{ Correct the ferredoxin domain alignment for FER1\_SPIOL by
inserting two additional gaps after the gap at column 47. First press [ESC] to
clear the selection, then hold [SHIFT] and click and drag on the G and move it
two columns to the right.}

\exstep{ Now complete the
alignment of FER1\_SPIOL with a locked edit by pressing [ESC] and select
columns 47 to 57 of the FER1\_SPIOL row. Move the mouse onto the G at column 50,
hold [SHIFT] and drag the G in column 47 of FER1\_SPIOL to the left by one
column to insert a gap at column 57.}

\exstep{ In the next two steps you will complete the alignment of the last two 
sequences.

Select the last two sequences (FER1\_MAIZE and O80429\_MAIZE), then press [SHIFT]
and click and drag the initial methionine of O80429\_MAIZE 5 columns to the right
so it lies at column 10.

Keep holding [SHIFT] and click and drag to insert
another gap at the proline at column 25 (25C in cursor mode). Remove the gap at
column 44, and insert 4 gaps at column 47 (after AAPM).}

\exstep{ Hold [SHIFT] and drag the I at column 39 of FER1\_MAIZE 2 columns to the
right. Remove the gap at FER1\_MAIZE column 49 by [SHIFT]-click and drag left by
one column. Press [ESC] to clear the selection, and then insert three gaps in
FER1\_MAIZE at column 47 by holding [SHIFT] and click and drag the S in FER1\_MAIZE to the right by three columns. Finally,
remove the gap in O80429\_MAIZE at column 56 using [SHIFT]-drag to the left on
56C.}

\exstep{ Use the
{\sl Edit $\Rightarrow$ Undo Edit} and {\sl Edit $\Rightarrow$ Redo Edit} menu
option, or their keyboard shortcuts ([CTRL]-Z and [CTRL]-Y) to step 
backwards and replay the edits you have made.}
}

\subsection{Sliding Sequences}
Pressing the [$\leftarrow$] or [$\rightarrow$] arrow keys when one or more
sequences are selected will ``slide'' the entire selected sequences to the left
or right (respectively). Slides occur regardless of the region selection -
which, for example, allows you to easily reposition misaligned subfamilies
within a larger alignment.
% % better idea to introduce hiding sequences, and use the invert selection, hide
% others, to simplify manual alignment construction

\subsection{Editing in Cursor mode}
Gaps can be easily inserted when in cursor mode (toggled with [F2]) by
pressing [SPACE]. Gaps will be inserted at the cursor, shifting the residue
under the cursor to the right. To insert {\sl n} gaps type {\sl n} and then
press [SPACE]. To insert gaps into all sequences of a group, use [CTRL]-[SPACE]
or [SHIFT]-[SPACE] (both keys held down together).

Gaps can be removed in cursor mode by pressing [BACKSPACE]. First make sure you
have everything unselected by pressing ESC. The gap under the cursor will be
removed. To remove {\sl n} gaps, type {\sl n} and then press [BACKSPACE]. Gaps
will be deleted up to the number specified. To delete gaps from all sequences of
a group, press [CTRL]-[BACKSPACE] or [SHIFT]-[BACKSPACE] (both keys held down
together). Note that the deletion will only occur if the gaps are in the same
columns in all sequences in the selected group, and those columns are to the
right of the selected residue.


\exercise{Keyboard Edits}
{This continues on from the previous exercise, and recreates the final part of the example ferredoxin
alignment from the unaligned sequences using Jalview's keyboard editing mode.

{\bf Window users:} Please {\em only use} [SHIFT]-[SPACE] in this
exercise.

{\bf Mac users:} [CTRL]-[SPACE] can also be used instead of [SHIFT]-[SPACE].

\exstep{Load the sequence alignment at
\textsf{http://www.jalview.org/tutorial/unaligned.fa}, or continue using the
edited alignment.  If you continue from the
previous exercise, first right click on the sequence ID panel and select
{\sl Reveal All}. Enter cursor mode by pressing [F2].}
% TODO: BACKSPACE or DELETE WHEN SEQS ARE SELECTED WILL DELETE ALL SEQS JAL-783

\exstep{Insert 58 gaps at the start of the sequence 1 (FER\_CAPAA). Press
{\sl 58} then {\sl [SPACE]}. }

\exstep{Go down one sequence and select rows 2-5 as a block. Click on the second sequence ID (FER\_CAPAN).
 Hold down shift and click on the fifth (FER1\_PEA). }

\exstep{Insert 6 gaps at the start of this group. Go to column 1 row 2 by typing
{\sl 1,2} then press {\sl [RETURN]}. Now insert 6 gaps in all the sequences.
Type {\sl 6} then hold down {\sl [SHIFT]} and press {\sl [SPACE]}.}
\exstep{Now insert one gap at column 34 and another at 38. Insert 3 gaps at 47.
Press {\sl 34C} then {\sl [SHIFT]-[SPACE]}.  Press {\sl 38C} then
[SHIFT]-[SPACE].
Press {\sl 47C} then {\sl 3 [SHIFT-SPACE]} the first through fourth sequences
are now aligned.}
\exstep{The fifth sequence (FER1\_PEA) is poorly aligned. We will delete some gaps and add some new ones. Press {\sl [ESC]} to clear the selection. Navigate to the start of sequence 5 and delete 3 gaps. Press {\sl 1,5 [RETURN]} then {\sl 3 [BACKSPACE]} to delete three gaps. Go to column 31 and delete the gap. Press {\sl 31C [BACKSPACE]} .}
\exstep{ Similarly delete the gap now at column 34, then insert two gaps at
column 38.
Press {\sl 34C [BACKSPACE]  38C 2 [SPACE]}. Delete three gaps at column 44 and
insert one at column 47 by pressing {\sl 44C 3 [BACKSPACE] 47C [SPACE]}.  The top five sequences are 
now aligned.}}

\chapter{Colouring Sequences and Figure Generation}
\label{colouringfigures}
\section{Colouring Sequences}
\label{colours}

Colouring sequences is a key aspect of alignment presentation. Jalview allows
you to colour the whole alignment, or just specific groups. Alignment and
group colours are rendered
{\sl below} any other colours, such as those arising from sequence features
(these are described in Section \ref{featannot}). This means that if you
try to apply one of the colourschemes described in this section, and nothing
appears to happen, it may be that you have sequence feature annotation
displayed, and you may have to disable it using the {\sl View $\Rightarrow$
Show Features} option before you can see your colourscheme.

There are two main types of colouring styles: {\bf simple static residue}
colourschemes and {\bf dynamic schemes} which use conservation and consensus
analysis to control colouring. {\bf Hybrid colouring} is also possible, where
static residue schemes are modified using a dynamic scheme. The individual schemes are described in Section \ref{colscheme} below.

\subsection{Colouring the Whole Alignment}

\parbox[c]{3.75in}{The alignment can be coloured {\sl via} the {\sl Colour} menu option in the alignment window. Selecting the colour scheme causes all residues to be coloured. The menu is divided into three sections. The first section gives options for the behaviour of the menu options, the second lists static and dynamic colourschemes available for selection. The last gives options for making hybrid colourschemes using conservation shading or colourscheme thresholding. 

}\parbox[c]{3in}{
\centerline {
\includegraphics[width=2.5in]{images/colour2.pdf}
}
}

\subsection{Colouring a Group or Selection}

Selections or groups can be coloured in two ways. The first is {\sl via} the Alignment Window's {\sl Colour} menu as stated above,
 after first ensuring that the {\sl Apply Colour To All Groups} flag is {\bf
 not} selected.
 This must be turned {\sl off} specifically as it is {\sl on} by default. 
 When unticked, selections from the Colours menu will only change the colour for residues in the current selection, 
 or the alignment view's ``background colourscheme'' when no selection exists.

The second method is to select sequences and right click mouse to open pop-up
menu and select {\sl Selection $\Rightarrow$ Edit New Group $\Rightarrow$ Group
Colour} from context menu options
(Figure \ref{colgrp}). This only changes the colour of the current selection or group.

\begin{figure}[htbp]
\begin{center}
%TODO update group_col.pdf to show latest jalview group edit submenu
\includegraphics[width=4in]{images/group_col.pdf}
\caption{{\bf Colouring a group via the context menu.}}
\label{colgrp}
\end{center}
\end{figure}

\subsection{Shading by Conservation}
For many colour schemes, the intensity of the colour in a column can be scaled
by the degree of amino acid property conservation. Selecting {\sl Colour
$\Rightarrow$ By Conservation} enables this mode, and {\sl Modify
Conservation Threshold...} brings up a selection box (the {\sl Conservation
Colour Increment} dialog box) allowing the alignment colouring to be modified.
Selecting a higher value limits colouring to more highly conserved columns (Figure \ref{colcons}).

 \begin{figure}[htbp]
\begin{center}
\includegraphics[width=2in]{images/colourcons1.pdf}
\includegraphics[width=2in]{images/colourcons3.pdf}
\includegraphics[width=2in]{images/colourcons5.pdf}
\caption{{\bf Conservation Shading} The density of the ClustalX style residue colouring is controlled by the conservation threshold. The effect of 0\% (left), 50\% (center) and 100\% (right) thresholds are shown.
}
\label{colcons}
\end{center}
\end{figure}

\subsection{Thresholding by Percentage Identity}

`Thresholding' is another hybrid colour model where a residue is only coloured
if it is not excluded by an applied threshold. Selecting {\sl Colour $\Rightarrow$ Above Identity Threshold} brings up a selection box with a slider controlling the minimum percentage identity threshold to be applied. Selecting a higher threshold (by sliding to the right) limits the colouring to columns with a higher percentage identity (as shown by the Consensus histogram in the annotation panel).

\subsection{Colouring by Annotation}
\label{colourbyannotation}
\parbox[c]{3.2in}{
Any of the {\bf quantitative} annotations shown on an alignment can be used to
threshold or shade the whole alignment.\footnote{Please remember to turn off
Sequence Feature display to see the shading} 

The {\sl Colour $\Rightarrow$ By
Annotation} option opens a dialog which allows you to select which annotation
to use, the minimum and maximum shading colours or whether the original
colouring should be thresholded (the `Use original colours' option).

Default settings for minimum and maximum colours can be set in the Jalview
Desktop's preferences.  
}\parbox[c]{3in}{
\centerline{\includegraphics[width=2.8in]{images/col_byannot.pdf}}}

The {\bf per Sequence} option in the {\bf Colour By Annotation} dialog
allows each sequence to be shaded according to sequence associated annotation
rows, such as protein disorder scores. This functionality is described further
in Section \ref{protdisorderpred}.

\subsection{Colour Schemes} 

\label{colscheme}
Full details on each colour scheme can be found in the Jalview on-line help. A brief description of each one is provided below:

\subsubsection{ClustalX}


 \parbox[c]{3.5in}{This is an emulation of the default colourscheme used for alignments in ClustalX, a graphical interface for the ClustalW multiple sequence alignment program. Each residue in the alignment is assigned a colour if the amino acid profile of the alignment at that position meets some minimum criteria specific for the residue type. }
\parbox[c]{3in}{\includegraphics[width=2.75in]{images/col_clustalx.pdf}}

\subsubsection{Blosum62}

\parbox[c]{3.5in}{Gaps are coloured white. If a residue matches the consensus sequence residue at that position it is coloured dark blue. If it does not match the consensus residue but the Blosum62 matrix gives a positive score, it is coloured light blue.}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_blosum62.pdf}
}

\subsubsection{Percentage Identity}
\parbox[c]{3.5in}{
The Percent Identity option colours the residues (boxes and/or text) according to the percentage of the residues in each column that agree with the consensus sequence. Only the residues that agree with the consensus residue for each column are coloured.
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_percent.pdf}
}

\subsubsection{Zappo}
\parbox[c]{3.5in}{
The residues are coloured according to their physicochemical properties. The physicochemical groupings are Aliphatic/hydrophobic, Aromatic, Positive, Negative, Hydrophillic, conformationally special, and Cyst(e)ine.
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_zappo.pdf}
}

\subsubsection{Taylor}

\parbox[c]{3.5in}{
This colour scheme was devised by Willie Taylor and an entertaining description of its origin can be found in Protein Engineering, 
Vol 10 , 743-746 (1997).
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_taylor.pdf}
}

\subsubsection{Hydrophobicity}
\parbox[c]{3.5in}{
Residues are coloured according to the hydrophobicity table of Kyte, J., and Doolittle, R.F., J. Mol. Biol. 1157, 105-132, 1982. The most hydrophobic residues are coloured red and the most hydrophilic ones are coloured blue.
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_hydro.pdf}
}

\subsubsection{Helix Propensity}

\parbox[c]{3.5in}{
The residues are coloured according to their Chou-Fasman\footnote{\label{chou-fasman}Chou, PY and Fasman, GD. Annu Rev Biochem. 1978;47:251-76.} helix propensity. The highest propensity is magenta, the lowest is green.
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_helix.pdf}
}

\subsubsection{Strand Propensity}

\parbox[c]{3.5in}{
The residues are coloured according to their Chou-Fasman\textsuperscript{\ref{chou-fasman}} Strand propensity. The highest propensity is Yellow, the lowest is blue.
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_strand.pdf}
}



\subsubsection{Turn Propensity}
\parbox[c]{3.5in}{
The residues are coloured according to their Chou-Fasman\textsuperscript{\ref{chou-fasman}} turn propensity. The highest propensity is red, the lowest is cyan.
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_turn.pdf}
}

\subsubsection{Buried Index}
\parbox[c]{3.5in}{
The residues are coloured according to their Chou-Fasman\textsuperscript{\ref{chou-fasman}} burial propensity. The highest propensity is blue, the lowest is green.
}
\parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_buried.pdf}
}
 

\subsubsection{Nucleotide}
\parbox[c]{3.5in}{ Residues are coloured with four colours corresponding to the
four nucleotide bases. All non ACTG residues are uncoloured. See Section
\ref{workingwithnuc} for further information about working with nucleic acid
sequences and alignments.
} \parbox[c]{3in}{ \includegraphics[width=2.75in]{images/col_nuc.pdf} }

\subsubsection{Purine Pyrimidine}
\parbox[c]{3.5in}{ Residues are coloured according to whether the corresponding
nucleotide bases are purine (magenta) or pyrimidine (cyan) based. All non ACTG
residues are uncoloured. For further information about working with nucleic acid
sequences and alignments, see Section \ref{workingwithnuc}.
%and Section \ref{workingwithrna}

} \parbox[c]{3in}{ \includegraphics[width=2.75in]{images/col_purpyr.pdf} }

\subsubsection{RNA Helix Colouring}
\parbox[c]{3.5in}{ Columns are coloured according to their assigned RNA helix as
defined by a secondary structure annotation line on the alignment. Colours for
each helix are randomly assigned, and option only available when an RNA
secondary structure row is present on the alignment. 
% For more details see Section \ref{workingwithrna} 
} \parbox[c]{3in}{
\includegraphics[width=2.75in]{images/col_rnahelix.pdf} }

\subsubsection{User Defined}
This dialog allows the user to create any number of named colour schemes at
will. Any residue may be assigned any colour. The colour scheme can then be
named. If you save the colour scheme, this name will appear on the Colour menu
(Figure \ref{usercol}).


\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2.5in]{images/col_user1.pdf}
\includegraphics[width=2in]{images/col_user2.pdf}
\includegraphics[width=1.75in]{images/col_user3.pdf}
\caption{{\bf Creation of a user defined colour scheme.} Residue types are assigned colours (left). The profile is saved (center) and can then be accessed {\sl via} the {\sl Colour} menu (right).}
\label{usercol}
\end{center}
\end{figure}

\exercise{Colouring Alignments}{
\label{color}
Note: Before you begin this exercise, ensure that the {\sl Apply Colour
To All Groups} flag is not selected in {\sl Colour} menu in the alignment window.
% patch needed for 2.10 This must be turned {\sl off} specifically as it is on
% by default.

\exstep{Open a sequence alignment, for example the PFAM domain PF03460 in PFAM
seed database. Select the alignment menu option {\sl Colour $\Rightarrow$
ClustalX} and note the colour change. Now try all the other colour schemes in the {\sl Colour} menu. 
Note that some colour schemes do not colour all residues.}
\exstep{Colour the alignment using {\sl Colour  $\Rightarrow$ Blosum62}. Select a group
of around 4 similar sequences. Use the context menu (right click on the group)
option {\sl Selection $\Rightarrow$ Edit New Group $\Rightarrow$ Group Colour
$\Rightarrow$ Blosum62} to colour the selection. Notice how some residues which
were not coloured are now coloured. The calculations performed for dynamic
colouring schemes like Blosum62 are based on the selected group,
not the whole alignment (this also explains the colouring changes observed in exercise
\ref{exselect} during the group selection step).}
\exstep{Keeping the same selection as before, colour the complete alignment except
the group using {\sl Colour  $\Rightarrow$ Taylor}.
Select the menu option  {\sl Colour  $\Rightarrow$ By Conservation}. 
Slide the selector in the Conservation Colour Increment dialog box from side
to side and observe the changes in the alignment colouring in the selection and in the complete alignment.}
Note: Feature colours overlay residue colouring. The features colours can be
toggled off by going to {\sl View  $\Rightarrow$ Show Sequence Features}.

{\bf See the video at: \url{http://www.jalview.org/training/Training-Videos}.}
}


\exercise{User Defined Colour Schemes}{
\exstep{Load a sequence alignment. Select the alignment menu option {\sl Colour $\Rightarrow$ User Defined}. A dialog window will open.}
\exstep{Click on an amino acid button, then select a colour for that amino acid. Repeat till all amino acids are coloured to your liking.}
\exstep{ Insert a name for the colourscheme in the appropriate field and click {\sl Save Scheme}. You will be prompted for a file name in which to save the colour scheme. The dialog window can now be closed.}
\exstep{The new colour scheme appears in the list of colour schemes in the {\sl Colour} menu and can be selected in future Jalview sessions.

{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}} }

\section{Formatting and Graphics Output}
\label{layoutandoutput}
Jalview is a WYSIWIG alignment editor. This means that for most kinds of graphics output, 
the layout that is seen on screen will be the same as what is outputted in an
exported graphics file.
It is therefore important to pick the right kind of display layout prior to generating figures. 

\subsection{Multiple Alignment Views}

Jalview is able to create multiple independent visualizations of the same underlying alignment - these are called {\sl Views}. Because each view displays the same underlying data, any edits performed in one view will update the alignment or annotation visible in all views.

\parbox[c]{4in}{Alignment views are created using the {\sl View $\Rightarrow$ New View} option of the alignment window or by Pressing [CTRL]-T. This will create a new view with the same groups, alignment layout and display options as the current one. Pressing G will gather together Views as named tabs on the alignment window, and pressing X will expand gathered Views so they can be viewed simultaneously in their own separate windows. To delete a group, press [CTRL]-W.}\parbox[c]{2.75in}{
\begin{center}\centerline{
\includegraphics[width=2.5in]{images/mulv_tabs.pdf}}
\end{center}
}

% JBPNote make an excercise on views ?

\subsection{Alignment Layout}
Jalview provides two screen layout modes, unwrapped (the default) where the alignment is in one long line across the window, and wrapped, where the alignment is on multiple lines, each the width of the window. Most layout options are controlled by the Format menu option in the alignment window, and control the overall look of the alignment in the view (rather than just a selected region).

\subsubsection{Wrapped Alignments}
Wrapped alignments can be toggled on and off using the {\sl Format $\Rightarrow$ Wrap} menu option (Figure \ref{wrap}). Note that the annotation lines are also wrapped. Wrapped alignments are great for publications and presentations but are of limited use when working with large numbers of sequences. 

If annotations are not all visible in wrapped mode, expand the alignment window to view them. Note that alignment annotation (see Section \ref{featannot}) cannot be interactively created or edited in wrapped mode, and selection of large regions is difficult. 
\begin{figure}[htbp]
\begin{center}
\parbox[c]{2in}{\includegraphics[width=2in]{images/wrap1.pdf}}
\parbox[c]{4in}{\includegraphics[width=4in]{images/wrap2.pdf}}
\caption{{\bf Wrapping the alignment.}}
\label{wrap}
\end{center}
\end{figure}


\subsubsection{Fonts}

\parbox[c]{4in}{The text appearance in a view can be modified {\sl via} the {\sl Format $\Rightarrow$ Font\ldots} alignment window menu. This setting applies for all alignment and annotation text except for that displayed in tool-tips. Additionally, font size and spacing can be adjusted rapidly by clicking the middle mouse button and dragging across the alignment window.}
\parbox[c]{2in}{\centerline{\includegraphics[width=1.75in]{images/font.pdf}}}

\subsubsection{Numbering and Label Justification}
Options in the {\sl Format} menu are provided to control the alignment view, and provide a range of options to control the display of sequence and alignment numbering, the justification of sequence IDs and annotation row column labels on the annotation rows shown below the alignment.

\subsubsection{Alignment and Group Colouring and Appearance}
The display of hidden row/column markers and gap characters can be turned off with {\sl Format $\Rightarrow$ Hidden Markers} and {\sl Format $\Rightarrow$ Show Gaps}, respectively. The {\sl Text} and {\sl Colour Text} option controls the display of sequence text and the application of alignment and group colouring to it. {\sl Boxes } controls the display of the background area behind each residue that is coloured by the applied coloursheme.  

\subsubsection{Highlighting Nonconserved Symbols}
The alignment layout and group sub-menu both contain an option to hide
conserved symbols from the alignment display ({\sl Format $\Rightarrow$ Show
nonconserved } in the alignment window or {\sl Selection $\Rightarrow$ Group
$\Rightarrow$ Show Nonconserved} by right clicking on a group). This mode is useful when working with
alignments that exhibit a high degree of homology, because Jalview will only
display gaps or sequence symbols that differ from the consensus for each
column, and render all others with a `.'.
%TODO add a graphic to illustrate this.
\subsection{Annotation Ordering and Display}
% TODO: describe consensus, conservation, quality user preferences, and group
% annotation preferences.
The annotation lines which appear below the sequence alignment are described in
detail in Section \ref{featannot}. They can be hidden by toggling the {\sl View
$\Rightarrow$ Show Annotations} menu option. Additionally, each annotation line
can be hidden and revealed in the same way as sequences {\sl via} the
pop-up context menu on the annotation name panel (Figure \ref{annot}).
Annotations can be reordered by dragging the annotation line label on the annotation label panel. Placing the
mouse over the top annotation label brings up a resize icon on the left. When this is
displayed, Click-dragging up and down provides more space in the alignment window for viewing the annotations, and less space for the sequence alignment.

\begin{figure}
\begin{center}
\includegraphics[width=2.5in]{images/annot1.pdf}
\includegraphics[width=2.5in]{images/annot2.pdf}
\caption{{\bf Hiding Annotations} Annotations can either be hidden from the {\sl
View} menu (left) or individually from the context menu (right).}
\label{annot}
\end{center}
\end{figure}

\exercise{Alignment Layout}{
\label{exscreen}
\exstep{Start Jalview and open the URL \textsf{http://www.jalview.org/examples/exampleFile.jar}. 
Select {\sl Format $\Rightarrow$ Wrap} from the alignment window menu. 
Experiment with the various options from the {\sl Format} menu, for example adjust the ruler placement, 
sequence ID format and so on. }
\exstep{Hide all the annotation rows by toggling {\sl Annotations $\Rightarrow$
Show Annotations} from the alignment window menu. Reveal the annotations by selecting the same menu option.} \exstep{Deselect {\sl Format $\Rightarrow$ Wrap}. Right click on the
annotation row labels to bring up the context menu, then select {\sl
Hide This Row}. Bring up the context menu again and select {\sl
Show All Hidden Rows} to reveal them.}
\exstep{Annotations can be reordered by clicking and dragging the row to the desired position. Click on the {\sl Consensus} row and drag it upwards to just 
above {\sl Quality}. The rows should now be reordered. Features and annotations are covered in more detail in Section \ref{featannot}.}
\exstep{Move the mouse to the top left hand corner of the annotation labels - 
a grey up/down arrow symbol should appear - when this is shown, the height of the {\sl Annotation Area} can be changed 
by clicking and dragging this icon up or down.}
}

\subsection{Graphical Output}
\label{figuregen}
\parbox[c]{4in}{Jalview allows alignments figures to be exported in three different formats, each of which is suited to a particular purpose. Image export is {\sl via} the {\sl File $\Rightarrow$ Export Image $\Rightarrow$ \ldots } alignment window menu option. }
\parbox[c]{2in}{\centerline{\includegraphics[width=1.25in]{images/image.pdf}}}

\subsubsection{HTML}

\parbox[c]{3in}{HTML is the format used by web pages. Jalview outputs the alignment as an HTML table with all the colours and fonts as seen. Any additional annotation will also be embedded as sensitive areas on the page, such as URL links for each sequence's ID label. This file can then be viewed directly with any web browser. Each residue is placed in an individual table cell. Unwrapped alignments will produce a very wide page.}
\parbox[c]{3.5in}{\centerline{\includegraphics[width=3in]{images/image_html.pdf}}}

\subsubsection{EPS}
\parbox[c]{3in}{EPS is Encapsulated Postscript. {\bf It is the format of choice
for publications and posters} as it gives the highest quality output of any of
the image types. It can be scaled to any size, so will still look good on an A0
poster.
This format can be read by most good presentation and graphics packages such as Adobe Illustrator or Inkscape.
}
\parbox[c]{3.5in}{\centerline{\includegraphics[width=3in]{images/image_eps.pdf}} \par \centerline{Zoom Detail of EPS image.}}

\subsubsection{PNG}
\parbox[c]{3in}{
PNG is Portable Network Graphics. This output option produces an image that can be easily included in web pages and incorporated in presentations using e.g. Powerpoint or Open Office. It is a bitmap image so does not scale and is unsuitable for use on posters, or in publications.

For submission of alignment figures to journals, please use EPS\footnote{If the journal complains, {\em insist}.}.
}
\parbox[c]{3.5in}{\centerline{\includegraphics[width=3in]{images/image_png.pdf}} \par \centerline{Zoom Detail of PNG image.}}

 \exercise{Graphical Output}{
\exstep{Load the example Jalview Jar file in Exercise \ref{exscreen}. 
Customise it how you wish but leave it unwrapped. 
Select {\sl File $\Rightarrow$ Export Image $\Rightarrow$ HTML} from the alignment menu. 
Save the file and open it in your favoured web browser.  }
\exstep{Wrap the alignment and export the image to HTML again. Compare the two
images. (Note that the exported image matches the format displayed in the
alignment window but {\bf annotations are not exported}).}
\exstep{Export the alignment using the {\sl File $\Rightarrow$ Export Image $\Rightarrow$ PNG} menu option. 
Open the file in an image viewer that allows zooming such as Paint or Photoshop (Windows), or Preview (Mac OS X) and zoom in. 
Notice that the image is a bitmap and it becomes pixelated when zoomed. 
(Note that the {\bf annotation lines are included} in the image.)}
\exstep{Export the alignment using the {\sl File $\Rightarrow$ Export Image
$\Rightarrow$ EPS} menu option. Open the file in a suitable program such as
Photoshop, Illustrator, Inkscape, Ghostview, Powerpoint (Windows), or
Preview (Mac OS X). Zoom in and note that the image has near-infinite
resolution.} 
}

% left out for Glasgow 2016
% \newpage
% 
% \section{Summary - the rest of the manual}
% 
% The first few chapters have covered the basics of Jalview operation: from
% starting the program, importing, exporting, selecting, editing and colouring
% aligments, to the generation of figures for publication, presentation and web
% pages.
% 
% The remaining chapters in the manual cover:
% 
% \begin{list}{$\circ$}{}
% \item{Chapter \ref{featannot} covers the creation, manipulation and visualisation
% of sequence and alignment annotation, and retrieval of sequence and feature data
% from databases.}
% \item {Chapter \ref{msaservices} explores the range of multiple alignment
% programs offered via Jalview's web services, and introduces the use of
% AACon for protein multiple alignment conservation analysis.}
% \item {Chapter \ref{alignanalysis} introduces Jalview's built in tools for
% multiple sequence alignment analysis, including trees, PCA, and alignment
% conservation analysis. }
% \item {Chapter \ref{3Dstructure} demonstrates the structure visualization
% capabilities of Jalview.}
% \item {Chapter \ref{proteinprediction} introduces protein sequence based
% secondary structure and disorder prediction tools, including JPred.}
% \item {Chapter \ref{dnarna} covers the special functions and
% visualization techniques for working with RNA alignments and protein coding
% sequences.}
% \item {Chapter \ref{jvwebservices} provides instructions on the
% installation of your own Jalview web services.}
% \end{list}

\chapter{Annotation and Features}
\label{featannot}
Annotations and features are additional information that is
overlaid on the sequences and the alignment.
Generally speaking, annotations reflect properties of the alignment as a
whole, often associated
with columns in the alignment. Features are often associated with specific
residues in the sequence.

Annotations are shown below the alignment in the annotation panel, the
properties are often based on the alignment.
Conversely, sequence features are properties of the individual sequences, so they do not change with the alignment, 
but are shown mapped on to specific residues within the alignment. 

Features and annotation can be interactively created, or retrieved from external
data sources. Webservices like JPred (see \ref{jpred} above) can be used to
analyse a given sequence or alignment and generate annotation for it.


\section{Conservation, Quality and Consensus Annotation}
\label{annotationintro}
Jalview automatically calculates several quantitative alignment annotations
which are displayed as histograms below the multiple sequence alignment columns. 
Conservation, quality and consensus scores are examples of dynamic
annotation, so as the alignment changes, they change along with it.
The scores can be used in the hybrid colouring options to shade the alignments. 
Mousing over a conservation histogram reveals a tooltip with more information.

These annotations can be hidden and deleted via the context menu linked to the
annotation row; but they are only created on loading an alignment. If they are
deleted then the alignment should be saved and then reloaded to restore them.
Jalview provides a toggle to autocalculate a consensus sequence upon editing. This is normally selected by default, but can be turned off for
large alignments {\sl via} the {\sl Calculate $\Rightarrow$ Autocalculate
Consensus} menu option if the interface is too slow.

\subsubsection{Conservation Annotation}

Alignment conservation annotation is quantitative numerical index reflecting the
conservation of the physico-chemical properties for each column of the alignment. 
The calculation is based on AMAS method of multiple sequence alignment analysis (Livingstone C.D. and Barton G.J. (1993) CABIOS Vol. 9 No. 6 p745-756), 
with identities scoring highest, and amino acids with substitutions in the same physico-chemical class have next highest score. 
The score for each column is shown below the histogram. 
The conserved columns with a score of 11 are indicated by '*'.
Columns with a score of 10 have mutations but all properties are conserved are marked with a '+'.

\subsubsection{Consensus Annotation}

Alignment consensus annotation reflects the percentage of the different residue
per column. By default this calculation includes gaps in columns, gaps can be ignored via the Consensus label context 
menu to the left of the consensus bar chart. 
The consensus histogram can be overlaid
with a sequence logo that reflects the symbol distribution at each column of
the alignment. Right click on the Consensus annotation row and select the {\sl Show
Logo} option to display the Consensus profile for the group or alignment.
Sequence logos can be enabled by default for all new alignments {\sl via} the
Visual tab in the Jalview desktop's preferences dialog box.

\subsubsection{Quality Annotation}

Alignment quality annotation is an ad-hoc measure of the likelihood of observing
the mutations (if any) in a particular column of the alignment. The quality score is calculated for each column in an alignment by summing, 
for all mutations, the ratio of the two BLOSUM 62 scores for a mutation pair and each residue's conserved BLOSUM62 score (which is higher). 
This value is normalised for each column, and then plotted on a scale from 0 to 1.

\subsubsection{Group Associated Annotation}
\label{groupassocannotation}
Group associated consensus and conservation annotation rows reflect the
sequence variation within a particular group. Their calculation is enabled
by selecting the {\sl Group Conservation} or {\sl Group Consensus} options in
the {\sl Annotation $\Rightarrow$ Autocalculated Annotation } submenu of the
alignment window. 

\subsection{Creating User Defined Annotation}

To create a new annotation row, right click on the annotation label panel and select the {\sl Add New Row} menu option (Figure \ref{newannotrow}).
A dialog box appears. Enter the label to use for this row and a new row will appear.

To create a new annotation, first select all the positions to be annotated on the appropriate row. 
Right-clicking on this selection brings up the context menu which allows the insertion of graphics for secondary structure ({\sl Helix} or {\sl Sheet}), 
text {\sl Label} and the colour in which to present the annotation (Figure \ref{newannot}). On selecting {\sl Label} a dialog box will appear, 
requesting the text to place at that position. After the text is entered, the selection can be removed and the annotation becomes clearly 
visible\footnote{When annotating a block of positions, the text can be partly obscured by the selection highlight. Pressing the  [ESC] key clears 
the selection and the label is then visible.}. Annotations can be coloured or deleted as desired.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=1.3in]{images/annots1.pdf}
\includegraphics[width=2in]{images/annots2.pdf}
\caption{{\bf Creating a new annotation row.} Annotation rows can be reordered by dragging them to the desired place.}
\label{newannotrow}
\end{center}
\end{figure}

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2in]{images/annots3.pdf}
\includegraphics[width=2in]{images/annots4.pdf}
\includegraphics[width=2in]{images/annots5.pdf}
\caption{{\bf Creating a new annotation.} Annotations are created from a selection on the annotation row and can be coloured as desired.}
\label{newannot}
\end{center}
\end{figure}

\subsection{Automated Annotation of Alignments and Groups}

On loading a sequence alignment, Jalview will normally\footnote{Automatic
annotation can be turned off in the {\sl Visual } tab in the {\sl Tools
$\Rightarrow$ Preferences } dialog box.} calculate a set of automatic annotation
rows which are shown below the alignment. For nucleotide sequence alignments,
only an alignment consensus row will be shown, but for amino acid sequences,
alignment quality (based on BLOSUM 62) and physicochemical conservation will
also be shown. Conservation is calculated according to Livingstone and
Barton\footnote{{\sl ``Protein Sequence Alignments: A Strategy for the
Hierarchical Analysis of Residue Conservation." } Livingstone C.D. and Barton
G.J. (1993) {\sl CABIOS } {\bf 9}, 745-756}.
Consensus is the modal residue (or {\tt +} where there is an equal top residue).
The inclusion of gaps in the consensus calculation can be toggled by
right-clicking on the Consensus label and selecting {\sl Ignore Gaps in
Consensus} from the pop-up context menu located with consensus annotation row.
Quality is a measure of the inverse likelihood of unfavourable mutations in the alignment. Further details on these
calculations can be found in the on-line documentation.


\exercise{Annotating Alignments}{
  \label{annotatingalignex}
\exstep{Load the alignment at \textsf{http://www.jalview.org/tutorial/alignment.fa}. 
Right-click on the {\sl Conservation} annotation row to
bring up the context menu and select {\sl Add New Row}. A dialog box will
appear asking for {\sl Annotation Name} and {\sl Annotation Description}.
Enter ``Iron binding site" and click {\sl OK}. A new, empty, row appears.
}
\exstep{
Navigate to column 97. Move down and on the new annotation row called
``Iron binding site, select column 97.
Right click at this selection and select {\sl Label} from the context menu.
Enter ``Fe" in the box and click {\sl OK}. Right-click on the selection again
and select {\sl Colour}.
Choose a colour from the colour chooser dialog 
and click {\sl OK}. Press [ESC] to remove the selection.

{\sl Note: depending on your Annotation sort settings, your newly
created annotation row might 'jump' to the top or bottom of the annotation
panel. Just scroll up or down to find it again - the column you marked will
still be selected. }

}
\exstep{ Select columns 70-77 on the annotation row. Right-click and choose {\sl Sheet} from the
 context menu. You will be prompted for a label. Enter ``B" and press {\sl OK}. A new line showing the 
 sheet as an arrow appears. The colour of the label can be changed but not the colour of the sheet 
 arrow. 
}
\exstep{Right click on the title text of annotation row that you just created. 
Select {\sl Export Annotation} in context menu and, in the Export Annotation
dialog box that will open, select the Jalview format and click the {\sl [To Textbox]} button. 

The format for this file is given in the Jalview help. Press [F1] to open it, and find 
the ``Annotations File Format'' entry in the ``Alignment Annotations'' section of the contents 
pane. }

\exstep{Export the file to a text editor and edit the file to change the name of the annotation 
row. Save the file and drag it onto the alignment view.}
\exstep{Add an additional helix somewhere along the row by editing the file and 
re-importing it.

{\sl Hint: Use the Export Annotation function to view what helix annotation looks like in 
a Jalview annotation file.}}
\exstep{Use the {\sl Alignment Window $\Rightarrow$ File $\Rightarrow$ Export Annotations...} 
function to export all the alignment's annotation to a file.}
\exstep{Open the exported annotation in a text editor, and use the Annotation File Format 
documentation to modify the style of the Conservation, Consensus and Quality annotation rows so 
they appear as several lines on a single line graph.

{\sl Hint: You need to change the style of annotation row in the first field of the annotation 
row entry in the file, and create an annotation row grouping to overlay the three quantitative 
annotation rows.}
}
\exstep{{\bf Homework for after you have completed exercise \ref{secstrpredex}:}
\label{viewannotfileex}
      
Recover or recreate the secondary structure predictions that you made from
JPred. Use the {\sl File $\Rightarrow$ Export Annotation} function to view the Jnet secondary structure prediction annotation row.

Note the 
SEQUENCE\_REF statements surrounding the row specifying the sequence association for the 
annotation. 
}}


\section{Importing Features from Databases}
\label{featuresfromdb}
Jalview supports feature retrieval from public databases.
It includes built in parsers for Uniprot and ENA (or EMBL) records retrieved
from the EBI. Sequences retrieved from these sources using the sequence fetcher (see
Section \ref{fetchseq}) will already possess features.

\subsection{Sequence Database Reference Retrieval}
\label{fetchdbrefs}
Jalview maintains a list of external database references for each sequence in
an alignment. These are listed in a tooltip when the mouse is moved over the
sequence ID when the {\sl View $\Rightarrow$ Sequence ID Tooltip $\Rightarrow$
Show Database Refs } option is enabled. Sequences retrieved using the sequence
fetcher will always have at least one database reference, but alignments
imported from an alignment file generally have no database references.

\subsubsection{Database References and Sequence Coordinate Systems}

Jalview displays features in the local sequence's coordinate system which is
given by its `start' and `end'. Any sequence features on the sequence will be
rendered relative to the sequence's start position. If the start/end positions
do not match the coordinate system from which the features were defined, then
the features will be displayed incorrectly.

\subsubsection{Viewing and Exporting a Sequence's Database Annotation}

You can export all the database cross references and annotation terms shown in
the sequence ID tooltip for a sequence by right-clicking and selecting the {\sl
[Sequence ID] $\Rightarrow$ Sequence details \ldots} option from the popup
menu.
A similar option is provided in the {\sl Selection} sub-menu allowing you to
obtain annotation for the sequences currently selected. 

\parbox[l]{3.4in}{
The {\sl Sequence Details
\ldots} option will open a window containing the same text as would be shown in
the tooltip window, including any web links associated with the sequence. The
text is HTML, and options on the window allow the raw code to be copied and
pasted into a web page.}
\parbox[c]{3in}{
\centerline{\includegraphics[width=2.2in]{images/seqdetailsreport.pdf}}}

\subsubsection{Automatically Discovering a Sequence's Database References}
Jalview includes a function to automatically verify and update each sequence's
start and end numbering against any of the sequence databases that the {\sl
Sequence Fetcher} has access to. This function is accessed from the {\sl
Webservice $\Rightarrow$ Fetch DB References} sub-menu in the Alignment
window. This menu allows you to query either the set of {\sl Standard
Databases}, which includes EMBL, Uniprot, the PDB, or just a specific datasource from one of the submenus.
When one of the entries from this menu is selected, Jalview will use the ID
string from each sequence in the alignment or in the currently selected set to
retrieve records from the external source. Any sequences that are retrieved are
matched against the local sequence, and if the local sequence is found to be a
sub-sequence of the retrieved sequence then the local sequence's start/end
numbering is updated.  A new database reference mapping is created, mapping the
local sequence to the external database, and the local sequence inherits any
additional annotation retrieved from the database sequence.

The database retrieval process terminates when a valid mapping is found for a
sequence, or if all database queries failed to retrieve a matching sequence.
Termination is indicated by the disappearance of the moving progress indicator
on the alignment window. A dialog box may be shown once it completes which
lists sequences for which records were found, but the sequence retrieved from
the database did not exactly contain the sequence given in the alignment (the
{\sl ``Sequence not 100\% match'' dialog box}).


\subsubsection{The Fetch Uniprot IDs Dialog Box}
\label{discoveruniprotids}
If any sources are selected which refer to Uniprot coordinates as their reference system, 
then you may be asked if you wish to retrieve Uniprot IDs for your sequence. Pressing OK instructs Jalview to verify the sequences against Uniprot records retrieved using the sequence's ID string. This operates in much the same way as the {\sl Web Service $\Rightarrow$ Fetch Database References } function described in Section \ref{fetchdbrefs}. 
If a sequence is verified, then the start/end numbering will be adjusted to match the Uniprot record. 

\subsubsection{Rate of Feature Retrieval}
Feature retrieval can take some time if a large number of sources are selected
and if the alignment contains a large number of sequences.  
As features are retrieved, they are immediately added to the current alignment view.
The retrieved features are shown on the sequence and can be customised as described previously.


\subsection{Colouring Features by Score or Description
Text}
\label{featureschemes}
Sometimes, you may need to visualize the differences in information carried by
sequence features of the same type. This is most often the case when features
of a particular type are the result of a specific type of database query or calculation. Here, they may also carry information within their textual description, or most commonly for calculations, a score related to the property being investigated. Jalview can shade sequence
features using a graduated colourscheme in order to highlight these variations.
In order to apply a graduated scheme to a feature type, select the `Graduated
colour' entry in the Sequence {\sl Feature Type}'s popup menu, which is opened by
right-clicking the {\sl Feature Type} or {\sl Color} in the {\sl Sequence Feature Settings} dialog box. Two types
of colouring styles are currently supported: the default is quantitative
colouring, which shades each feature based on its score, with the highest
scores receiving the `Max' colour, and the lowest scoring features coloured
with the `Min' colour. Alternately, you can select the `Colour by label'
option to create feature colours according to the description text associated
with each feature. This is useful for general feature types - such as
Uniprot's `DOMAIN' feature - where the actual type of domain is given in the
feature's description.

Graduated feature colourschemes can also be used to exclude low or
high-scoring features from the alignment display. This is done by choosing your
desired threshold type (either above or below), using the drop-down menu in the
dialog box. Then, adjust the slider or enter a value in the text box to set the
threshold for displaying this type of feature.

The feature settings dialog box allows you to toggle between a graduated and
simple feature colourscheme using the pop-up menu for the feature type. When a
graduated scheme is applied, it will be indicated in the colour column for
that feature type - with coloured blocks or text to indicate the colouring
style and a greater than ($>$) or less than ($<$) symbol to indicate when a
threshold has been defined.

\subsection{Using Features to Re-order the Alignment}
\label{featureordering}
The presence of sequence features on certain sequences or in a particular
region of an alignment can quantitatively identify important trends in
the aligned sequences. In this case, it is more useful to
re-order the alignment based on the number of features or their associated scores, rather than simply re-colour the aligned sequences. The sequence feature settings
dialog box provides two buttons: `Seq sort by Density' and `Seq sort by
Score', that allow you to reorder the alignment according to the number of
sequence features present on each sequence, and also according to any scores
associated with a feature. Each of these buttons uses the currently displayed
features to determine the ordering, but
if you wish to re-order the alignment using a single type of feature, then you can do this from the {\sl Feature Type}'s
popup menu. Simply right-click the type's style in the Sequence Feature Settings dialog
box, and select one of the {\sl Sort by Score} and {\sl Sort by Density}
options to re-order the alignment. Finally, if a specific region is selected,
then only features found in that region of the alignment will be used to
create the new alignment ordering.
% \exercise{Shading and Sorting Alignments using Sequence Features}{
% \label{shadingorderingfeatsex}
% 
% This exercise is currently not included in the tutorial because no DAS servers
% currently exist that yield per-residue features for any Uniprot sequence. 
% 
% \exstep{Re-load the alignment from \ref{dasfeatretrexcercise}.
% }
% \exstep{Open the
% feature settings panel, and, after first clearing the current
% selection, press the {\em Seq Sort by Density} button a few times.}
% \exstep{Use the DAS fetcher to retrieve the Kyte and Doolittle Hydrophobicity
% scores for the protein sequences in the alignment.
% {\sl Hint: the nickname for the das source is `KD$\_$hydrophobicity'.}}
% \exstep{Change the feature settings so only the hydrophobicity features are
% displayed. Mouse over the annotation and also export and examine the GFF and
% Jalview features file to better understand how the hydrophobicity measurements
% are recorded.}
% \exstep{Apply a {\sl Graduated Colour} to the hydrophobicity annotation to
% reveal the variation in average hydrophobicity across the alignment.}
% \exstep{Select a range of alignment columns, and use one of the sort by feature buttons to order the alignment according to that region's average
% hydrophobicity.}
% \exstep{Save the alignment as a project, for use in exercise
% \ref{threshgradfeaturesex}.} }
% 
% \exercise{Shading alignments with combinations of graduated feature
% colourschemes}{
% \label{threshgradfeaturesex}
% \exstep{Reusing the annotated alignment from exercise
% \ref{shadingorderingfeatsex}, experiment with the colourscheme threshold to
% highlight the most, or least hydrophobic regions. Note how the {\sl Colour} icon for the {\sl Feature Type} changes when you change the threshold type and press OK.}
% \exstep{Change the colourscheme so
% that features at the threshold are always coloured grey, and the most
% hydrophobic residues are coloured red, regardless of the threshold value
% ({\em hint - there is a switch on the dialog to do this for you}).}
% \exstep{Enable the Uniprot {\em chain} annotation in the feature settings
% display and re-order the features so it is visible under the hydrophobicity
% annotation.}
% \exstep{Apply a {\sl Graduated Colour} to the {\em chain}
% annotation so that it distinguishes the different canonical names associated
% with the mature polypeptide chains.}
% \exstep{Export the alignment's sequence features using the Jalview and GFF file formats, to see how the different types of graduated feature
% colour styles are encoded. }
% }

\subsection{Creating Sequence Features}
Sequence features can be created simply by selecting the area in a sequence (or sequences) to form the feature and selecting {\sl Selection $\Rightarrow$ Create Sequence Feature } from the right-click context menu (Figure \ref{features}). A dialog box allows the user to customise the feature with respect to name, group, and colour. The feature is then associated with the sequence. Moving the mouse over a residue associated with a feature brings up a tool tip listing all features associated with the residue.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2in]{images/feature1.pdf}
\includegraphics[width=2.5in]{images/feature2.pdf}
\includegraphics[width=1.5in]{images/feature3.pdf}
\caption{{\bf Creating sequence features.} Features can readily be created from selections via the context menu and are then displayed on the sequence. }
\label{features}
\end{center}
\end{figure}

Creation of features from a selection spanning multiple sequences results in the creation of one feature per sequence. 
Each feature remains associated with its own sequence.

\subsection{Customising Feature Display}

Feature display can be toggled on or off by selecting the {\sl View
$\Rightarrow$ Show Sequence Features} menu option. When multiple features are
present it is usually necessary to customise the display. Jalview allows the
display, colour, rendering order and transparency of features to be modified
{\sl via} the {\sl View $\Rightarrow$ Feature Settings\ldots} menu option. This
brings up a dialog window (Figure \ref{custfeat}) which allows the
visibility of individual feature types to be selected, colours changed (by
clicking on the colour of each sequence feature type) and the rendering order
modified by dragging feature types to a new position in the list. Dragging the
slider alters the transparency of the feature rendering. The Feature
Settings dialog also includes functions for more advanced feature shading
schemes and buttons for sorting the alignment according to the distribution of
features. These capabilities are described further in sections
\ref{featureschemes} and \ref{featureordering}.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=4in]{images/features4.pdf}
\caption{{\bf Multiple sequence features.} An alignment with JPred secondary structure prediction annotation below it, and many sequence features overlaid onto the aligned sequences. The tooltip lists the features annotating the residue below the mouse-pointer.}
\end{center}
\end{figure}

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=4in]{images/features5.pdf}
\caption{{\bf Customising sequence features.} Features can be recoloured, switched on or off and have the rendering order changed. }
\label{custfeat}
\end{center}
\end{figure}

\subsection{Sequence Feature File Formats}

Jalview supports the widely used GFF tab delimited format\footnote{see
http://www.sanger.ac.uk/resources/software/gff/spec.html} and its own Jalview
Features file format for the import of sequence annotation. Features and
alignment annotation are also extracted from other formats such as Stockholm,
and AMSA. URL links may also be attached to features. See the online
documentation for more details of the additional capabilities of the Jalview
features file.

\exercise{Creating Features}{
\exstep{Open the alignment at \textsf{http://www.jalview.org/tutorial/alignment.fa}. 
We know that the Cysteine residues at columns 97, 102, 105 and 135 are involved in 
iron binding so we will create them as features. Navigate to column 97, sequence 1. 
Select the entire column by clicking in the ruler bar. Then right-click on the selection 
to bring up the context menu and select {\sl Selection $\Rightarrow$ Create Sequence Feature}. 
A dialog box will appear.
}
\exstep{
Enter a suitable Sequence Feature Name  (e.g. ``Iron binding site") in the
appropriate box. Click on the Feature Colour bar to change the colour if
desired, add a short description (``One of four Iron binding Cysteines") and
press {\sl OK}. The features will then appear on the sequences. } \exstep{Roll
the mouse cursor over the new features.
Note that the position given in the tool tip is the residue number, not the column number. 
To demonstrate that there is one feature per sequence, clear all selections by pressing [ESC] then insert a gap in sequence 3 at column 95.
Roll the mouse over the features and you will see that the feature has moved with the sequence. Delete the gap you created.
}
\exstep{
Add a similar feature to column 102. When the feature dialog box appears, clicking the Sequence Feature 
Name box brings up a list of previously described features. Using the same Sequence Feature Name allows the features to be grouped.}
\exstep{Select {\sl View $\Rightarrow$ Feature Settings\ldots} from the
alignment window menu. The Sequence Feature Settings window will appear. Move
this so that you can see the features you have just created. Click the check
box for ``Iron binding site"  under {\sl Display} and note that display of this
feature type is now turned off. Click it again and note that the features are
now displayed. Close the sequence feature settings box by clicking {\sl OK} or
{\sl Cancel}.} }

\chapter{Multiple Sequence Alignment}
\label{msaservices}
Sequences can be aligned using a range of algorithms provided by JABA web
services, including ClustalW\footnote{{\sl ``CLUSTAL W:
improving the sensitivity of progressive multiple sequence alignment through sequence
weighting, position specific gap penalties and weight matrix choice."} Thompson
JD, Higgins DG, Gibson TJ (1994) {\sl  Nucleic Acids Research} {\bf 22},
4673-80}, Muscle\footnote{{\sl ``MUSCLE: a multiple sequence alignment method
with reduced time and space complexity"} Edgar, R.C.
(2004) {\sl BMC Bioinformatics} {\bf 5}, 113},  MAFFT\footnote{{\sl ``MAFFT: a
novel method for rapid multiple sequence alignment based on fast Fourier
transform"}  Katoh, K., Misawa, K., Kuma, K. and Miyata, T. (2002) {\sl Nucleic
Acids Research} {\bf 30}, 3059-3066.  and {\sl ``MAFFT version 5:
improvement in accuracy of multiple sequence alignment"} Katoh, K., Kuma, K.,
Toh, H. and Miyata, T. (2005) {\sl Nucleic Acids Research} {\bf 33}, 511-518.},
ProbCons,\footnote{PROBCONS: Probabilistic Consistency-based Multiple Sequence
Alignment.
Do, C.B., Mahabhashyam, M.S.P., Brudno, M., and Batzoglou, S.
(2005) {\sl Genome Research} {\bf 15} 330-340.} T-COFFEE\footnote{T-Coffee:
A novel method for multiple sequence alignments. (2000) Notredame, Higgins and
Heringa {\sl JMB} {\bf 302} 205-217} and Clustal Omega.\footnote{Fast, scalable
generation of high-quality protein multiple sequence alignments using Clustal
Omega. Sievers F, Wilm A, Dineen DG, Gibson TJ, Karplus K, Li W, Lopez R,
McWilliam H, Remmert M, Soding J, Thompson JD, Higgins DG (2011) {\sl Molecular
Systems Biology} {\bf 7} 539
\href{http://dx.doi.org/10.1038/msb.2011.75}{doi:10.1038/msb.2011.75}} Of these,
T-COFFEE is slow but accurate. ClustalW is historically
the most widely used. Muscle is fast and probably best for
smaller alignments. MAFFT is probably the best for large alignments,
however Clustal Omega, released in 2011, is arguably the fastest and most
accurate tool for protein multiple alignment.

\section{Performing a multiple sequence alignment}
To run an alignment web service, select the appropriate method from the {\sl
Web Service $\Rightarrow$  Alignment $\Rightarrow$ \ldots} submenu (Figure
\ref{webservices}). For each service you may either perform an alignment with
default settings, use one of the available presets, or customise the parameters
with the `{\sl Edit and Run ..}' dialog box. Once the job is submitted, a
progress window will appear giving information about the job and any errors that
occur. After successful completion of the job, a new alignment window is opened
with the results, in this case an alignment. By default, the new alignment will be
ordered in the same way as the input sequences. Note: many alignment
programs re-order the input during their analysis and place homologous
sequences close together, the MSA algorithm ordering can be recovered
using the `Algorithm ordering' entry within the {\sl Calculate $\Rightarrow$
Sort } sub menu.

\subsection{Realignment to add sequences to an existing alignment}
The re-alignment option is currently only supported by Clustal  
Omega and ClustalW. When performing a re-alignment, Jalview submits the
current selection to the alignment service complete with any existing gaps.
Realignment with ClustalW is useful when one wishes to align
additional sequences to an existing alignment without any further optimisation
to the existing alignment. ClustalO's realignment works by generating a
probabilistic model (a.k.a HMM) from the original alignment, and then realigns
{\bf all} sequences to this profile. For a well aligned MSA, this process
will simply reconstruct the original alignment (with additonal sequences), but
in the case of low quality MSAs, some differences may be introduced.

\begin{figure}[htbp]
\begin{center}
\parbox[c]{1.5in}{\includegraphics[width=1.5in]{images/ws1.pdf}}
\parbox[c]{2.5in}{\includegraphics[width=2.5in]{images/ws2.pdf}}
\parbox[c]{2in}{\includegraphics[width=2in]{images/ws3.pdf}}
\caption{{\bf Multiple alignment via web services} The appropriate method is
selected from the menu (left), a status box appears (centre), and the results
appear in a new window (right).}
\label{webservices}
\end{center}
\end{figure}

\subsection{Alignments of Sequences that include Hidden Regions}
If the view or selected region submitted for alignment contains hidden
regions, then {\bf only the visible sequences will be submitted to the service}.
Furthermore, each contiguous segment of sequences will be aligned independently
(resulting in a number of alignment `subjobs' appearing in the status window).
Finally, the results of each subjob will be concatenated with the hidden regions
in the input data prior to their display in a new window. This approach ensures
that 1) hidden column boundaries in the input data are preserved in the
resulting alignment - in a similar fashion to the constraint that hidden columns
place on alignment editing (see Section \ref{lockededits} and 2) hidden
columns can be used to preserve existing parts of an alignment whilst the
visible parts are locally refined.

\subsection{Alignment Service Limits}
Multiple alignment is a computationally intensive calculation. Some JABA server
services and service presets only allow a certain number of sequences to be
aligned. The precise number will depend on the server that you are using to
perform the alignment. Should you try to submit more sequences than a service
can handle, then an error message will be shown informing you of the maximum
number allowed by the server.

\exercise{Multiple Sequence Alignment}{
\exstep{ Close all windows and open the alignment at {\sf
http://www.jalview.org/tutorial/unaligned.fa}.  Select {\sl
Web Service $\Rightarrow$ Alignment $\Rightarrow$ Muscle with Defaults}. 
A window will open giving the job status. After a short time, a second window will open
 with the results of the alignment.} 
 \exstep{Return to the first sequence alignment window by clicking on 
 the window, and repeat using {\sl ClustalO} (Omega) and {\sl MAFFT}, from the
 {\sl Web Service $\Rightarrow$ Alignment} menu, using the same initial
 alignment.
 Compare them and you should notice small differences. }
\exstep{Select the last three sequences in the MAFFT alignment, and de-align them 
with {\sl Edit $\Rightarrow$ Remove All Gaps}. Press [ESC] to deselect these
sequences. Then submit this view for re-alignment with {\sl ClustalO}.}
\exstep{Return to the alignment window in section (c), use [CTRL]-Z (undo) to
recover the alignment of the last three sequences in this MAFFT alignment.
Once the ClustalO re-alignment has completed, compare the results of
re-alignment of the three sequences with their alignment in the original MAFFT result.}
\exstep{Select columns 60 to 125 in the original MAFFT alignment and hide them,
by right clicking the mouse to bring up context menu.
Select {\sl Web Service $\Rightarrow$ Alignment $\Rightarrow$ Mafft with Defaults} to 
submit the visible portion of the alignment to MAFFT. When the web service job pane appears, 
note that there are now two alignment job status panes shown in the window.}
\exstep{When the MAFFT job has finished, compare the alignment of the N-terminal visible 
region in the result with the corresponding region of the original alignment.}
\exstep {If you wish, 
select and hide a few more columns in the N-terminal region, and submit the alignment to the 
service again and explore the effect of local alignment on the non-homologous parts of the 
N-terminal region.}
{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
}

\section{Customising the Parameters used for Alignment}

JABA web services allow you to vary the parameters used when performing a
bioinformatics analysis. For JABA alignment services, this means you are
usually able to modify the following types of parameters:
\begin{list}{$\bullet$}{}
\item{Amino acid or nucleotide substitution score matrix}
\item{Gap opening and widening penalties}
\item{Types of distance metric used to construct guide trees}
\item{Number of rounds of re-alignment or alignment optimisation}  
\end{list}
\begin{figure}[htbc]
\center{
\includegraphics[width=3in]{images/jvaliwsparamsbox.pdf}
\caption{{\bf Jalview's JABA alignment service parameter editing dialog box}.}
\label{jwsparamsdialog} }
\end{figure}

\subsection{Getting Help on the Parameters for a Service}

Each parameter available for a method usually has a short description, which
Jalview will display as a tooltip, or as a text pane that can be opened under
the parameter's controls. In the parameter shown in Figure
\ref{clustalwparamdetail}, the description was opened by selecting the button on the left hand side. Online help for the
service can also be accessed, by right clicking the button and selecting a URL
from the pop-up menu that will open.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2.5in]{images/clustalwparamdetail.pdf}
\caption{{\bf ClustalW parameter slider detail}. From the ClustalW {\sl Clustal $\Rightarrow$ Edit settings and run ...} dialog box. }
\label{clustalwparamdetail}
\end{center}
\end{figure} 

\subsection{Alignment Presets}
The different multiple alignment algorithms available from JABA vary greatly in
the number of adjustable parameters, and it is often difficult to identify what
are the best values for the sequences that you are trying to align. For these
reasons, each JABA service may provide one or more presets -- which are
pre-defined sets of parameters suited for particular types of alignment
problem. For instance, the Muscle service provides the following presets:
\begin{list}{$\bullet$}{}
\item Large alignments (balanced)
\item Protein alignments (fastest speed)
\item Nucleotide alignments (fastest speed)
\end{list}

The presets are displayed in the JABA web services submenu, and can also be
accessed from the parameter editing dialog box, which is opened by selecting
the `{\sl Edit settings and run ...}' option from the web services menu. If you have used
a preset, then it will be mentioned at the beginning of the job status file shown
in the web service job progress window.

\subsection{User Defined Presets}
Jalview allows you to create your own presets for a particular service. To do
this, select the `{\sl Edit settings and run ...}' option for your service,
which will open a parameter editing dialog box like the one shown in Figure
\ref{jwsparamsdialog}.

The top row of this dialog allows you to browse the existing presets, and
when editing a parameter set, allows you to change its nickname. As you
adjust settings, buttons will appear at the top of the parameters dialog that
allow you to Revert or Update the currently selected user preset with your changes, Delete the current preset, or Create a new preset, if none exists with the given name. In addition to the parameter set name, you can also provide a short
description for the parameter set, which will be shown in the tooltip for the
parameter set's entry in the web services menu.

\subsubsection{Saving Parameter Sets}
When creating a custom parameter set, you will be asked for a file name to save
it. The location of the file is recorded in the Jalview user preferences in the
same way as a custom alignment colourscheme, so when Jalview is launched again,
it will show your custom preset amongst the options available for running the
JABA service.

% 
% \exercise{Creating and using user defined presets}{\label{createandusepreseex}
% \exstep{Import the file at
% \textsf{http://www.jalview.org/tutorial/fdx\_unaligned.fa} into jalview.}
% \exstep{Use the `{\slDiscover Database Ids}' function to recover the PDB cross
% references for the sequences.}
% \exstep{Align the sequences using the default ClustalW parameters.}
% \exstep{Use the `{\sl Edit and run..}'
% option to open the ClustalW parameters dialog box, and create a new preset using
% the following settings:
% \begin{list}{$\bullet$}{}
% \item BLOSUM matrix (unchanged)
% \item Gap Opening and End Gap penalties = 0.05
% \item Gap Extension and Separation penalties = 0.05
% \end{list}
% 
% As you edit the parameters, buttons will appear on the dialog box
% allowing you revert your changes or save your settings as a new parameter
% set.
% 
% Before you save your settings, remeber to give them a meaningful name by editing
% the text box at the top of the dialog box.
% }
% \exstep{Repeat the alignment using your new parameter set by selecting it from
% the {\sl ClustalW Presets menu}.} 
% \exstep{These sequences have PDB structures associated with them, so it is
% possible to compare the quality of the alignments.
% 
% Use the {\sl View all {\bf N}
% structures} option to calculate the superposition of 1fdn on 1fxd for both
% alignments (refer to section \ref{superposestructs} for instructions). Which
% alignment gives the best RMSD ? }
% \exstep{Apply the same alignment parameter settings to the example alignment
% (available from \textsf{http://www.jalview.org/examples/uniref50.fa}). 
% 
% Are there differences ? If not, why not ?
% }
% }

\section{Protein Alignment Conservation Analysis}
\label{aacons}
The {\sl Web Service $\Rightarrow$ Conservation} menu controls the computation
of up to 17 different amino acid conservation measures for the current alignment
view. The JABAWS AACon Alignment Conservation Calculation Service, which is used
to calculate these scores, provides a variety of standard measures described by
Valdar in 2002\footnote{Scoring residue conservation. Valdar (2002) {\sl
Proteins: Structure, Function, and Genetics} {\bf 43} 227-241.} as well as an efficient implementation of the SMERFs
score developed by Manning et al. in 2008.\footnote{SMERFS Score Manning et al. {\sl BMC
Bioinformatics} 2008, {\bf 9} 51 \href{http://dx.doi.org/10.1186/1471-2105-9-51}{doi:10.1186/1471-2105-9-51}}

\subsection{Enabling and Disabling AACon Calculations}
When the AACon Calculation entry in the {\sl Web Service $\Rightarrow$
Conservation} menu is ticked, AACon calculations will be performed every time
the alignment is modified. Selecting the menu item will enable or disable
automatic recalculation.

\subsection{Configuring which AACon Calculations are Performed}
The {\sl Web Service $\Rightarrow$ Conservation $\Rightarrow$ Change AACon
Settings ...} menu entry will open a web services parameter dialog for the
currently configured AACon server. Standard presets are provided for quick and
more expensive conservation calculations, and parameters are also provided to
change the way that SMERFS calculations are performed.
AACon settings for an alignment are saved in Jalview projects along with the
latest calculation results.

\subsection{Changing the Server used for AACon Calculations}
If you are working with alignments too large to analyse with the public JABAWS
server, then you will most likely have already configured additional JABAWS
servers. By default, Jalview will chose the first AACon service available from
the list of JABAWS servers available. If available, you can switch to use
another AACon service by selecting it from the {\sl Web Service $\Rightarrow$
Conservation $\Rightarrow$ Switch Server} submenu.

\chapter{Analysis of Alignments}
\label{alignanalysis}
Jalview provides support for sequence analysis in two ways. A number of
analytical methods are `built-in', these are accessed from the {\sl Calculate}
alignment window menu. Computationally intensive analyses are run outside
Jalview {\sl via} web services - and found under the
{\sl Web Service} menu. In this section, we describe the built-in analysis
capabilities common to both the Jalview Desktop and the JalviewLite applet.
 
\section{PCA}
Principal components analysis calculations create a spatial
representation of the similarities within the current selection or the whole alignment if no selection has been made. After
the calculation finishes, a 3D viewer displays each sequence as a point in
3D `similarity space'. Sets of similar sequences tend to lie near each other in
this space.
Note: The calculation is computationally expensive, and may fail for very large
sets of sequences - because the JVM has run out of memory. Memory issues, and
how to overcome them, were discussed in Section \ref{memorylimits}.

\subsubsection{What is PCA?}
Principal components analysis is a technique for examining the structure of
complex data sets. The components are a set of dimensions formed from the
measured values in the data set, and the principal component is the one with the
greatest magnitude, or length. The sets of measurements that differ the most
should lie at either end of this principal axis, and the other axes correspond
to less extreme patterns of variation in the data set.
In this case, the components are generated by an eigenvector decomposition of
the matrix formed from the sum of pairwise substitution scores at each aligned
position between each pair of sequences. The basic method is described in the
1995 paper by {\sl G. Casari, C. Sander} and {\sl A. Valencia} \footnote{{\sl
Nature Structural Biology} (1995) {\bf 2}, 171-8.
PMID: 7749921} and implemented at the SeqSpace server at the EBI.

Jalview provides two different options for the PCA calculation: SeqSpace and
Jalview mode. In SeqSpace mode, PCAs are computed using the identity matrix, and
gaps are treated as 'the unknown residue' (this actually differs from the
original SeqSpace paper, and will be adjusted in a future version of Jalview).
In Jalview mode, PCAs are computed using the chosen score matrix - which for
protein sequences, defaults to BLOSUM 62, and for nucleotides, is the
DNA identity matrix that also treats Us and Ts as identical, to support analysis
of both RNA and DNA alignments. The {\sl Change Parameters} allows the
calculation method and score models to be changed.\footnote{See
\url{http://www.jalview.org/help/html/calculations/pca.html}.}

\subsubsection{The PCA Viewer}

PCA analysis can be launched from the {\sl Calculate $\Rightarrow$ Principal
Component Analysis} menu option. {\bf PCA requires a selection containing at
least 4 sequences}.  A window opens containing the PCA tool (Figure \ref{PCA}).
Each sequence is represented by a small square, coloured by the background
colour of the sequence ID label. The axes can be rotated by clicking and
dragging the left mouse button and zoomed using the $\uparrow$ and $\downarrow$
keys or the scroll wheel of the mouse (if available).  A tool tip appears if the
cursor is placed over a sequence. Sequences can be selected by clicking on them.
[CTRL]-Click can be used to select multiple sequences.

Labels will be shown for each sequence by toggling the {\sl View $\Rightarrow$
Show Labels} menu option, and the plot background colour changed {\sl via} the
{\sl View $\Rightarrow$ Background Colour..} dialog box. A graphical
representation of the PCA plot can be exported as an EPS or PNG image {\sl via}
the {\sl File $\Rightarrow$ Save As $\Rightarrow$ \ldots } submenu.

\exercise{Principal Component Analysis}
{ \exstep{Load the alignment at
\textsf{http://www.jalview.org/tutorial/alignment.fa}.}
\exstep{Select the menu option {\sl Calculate $\Rightarrow$ Principal Component
Analysis}.
A new window will open. Move this window within the desktop so that the tree,
alignment and PCA viewer windows are all visible.
Try rotating the plot by clicking and dragging the mouse on the plot in the PCA window.
Note that clicking on points in the plot will highlight the sequences on the
alignment.
} \exstep{ Select {\sl Calculate $\Rightarrow$ Calculate Tree $\Rightarrow$
Neighbour Joining Using BLOSUM62}. A new tree window will appear.
Place the mouse cursor on the tree window so that the
tree partition location will divide the alignment into a number of groups, each of a different colour.
Note how the colour of the sequence ID label matches both the colour of
the partitioned tree and the points in the PCA plot.} 
{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
}

\begin{figure}[hbtp]
\begin{center}
\includegraphics[width=2in]{images/PCA1.pdf}
\includegraphics[width=3in]{images/PCA3.pdf}
\caption{{\bf PCA Analysis.} }
\label{PCA}
\end{center}
\end{figure}



\subsubsection{PCA Data Export}
Although the PCA viewer supports export of the current view, the plots produced
are rarely suitable for direct publication. The PCA viewer's {\sl File} menu
includes a number of options for exporting the PCA matrix and transformed points
as comma separated value (CSV) files. These files can be imported by tools such
as {\bf R} or {\bf gnuplot} in order to graph the data.

\section{Trees}
\label{trees}
Jalview can calculate and display trees, providing interactive tree-based
grouping of sequences though a tree viewer. All trees are calculated {\sl via}
the {\sl Calculate $\Rightarrow$ Calculate Tree $\Rightarrow$ \ldots} submenu.
Trees can be calculated from distance matrices determined from \% identity or
aggregate BLOSUM 62 score using either {\sl Average Distance} (UPGMA) or {\sl
Neighbour Joining} algorithms. The input data for a tree is either the selected
region or the whole alignment, excluding any hidden regions.

On calculating a tree, a new window opens (Figure \ref{trees1}) which contains
the tree. Various display settings can be found in the tree window {\sl View}
menu, including font, scaling and label display options. The {\sl File
$\Rightarrow$ Save As} submenu contains options for image and Newick file
export. Newick format is a standard file format for trees which allows them to
be exported to other programs.  Jalview can also read in external trees in
Newick format {\sl via} the {\sl File $\Rightarrow$ Load Associated Tree} menu
option. Leaf names on imported trees will be matched to the associated alignment
- unmatched leaves will still be displayed, and can be highlighted using the
{\sl View $\Rightarrow$ Mark Unlinked Leaves} menu option.


\begin{figure}
\begin{center}
\includegraphics[width=2.5in]{images/trees1.pdf}
\includegraphics[width=2.5in]{images/trees2.pdf}
\includegraphics[width=1.25in]{images/trees4.pdf}
\caption{{\bf Calculating Trees} Jalview provides a range of options 
for calculating trees.
Jalview can also load precalculated trees in Newick format (right).}
\label{trees1}
\end{center}
\end{figure}


Clicking on the tree brings up a cursor across the height of the tree. The
sequences are automatically partitioned and coloured (Figure \ref{trees2}). To
group them together, select the {\sl Calculate $\Rightarrow$ Sort $\Rightarrow$
By Tree Order $\Rightarrow$ \ldots} alignment window menu option and choose the
correct tree. The sequences will then be sorted according to the leaf order
currently shown in the tree view. The coloured background to the sequence IDs
can be removed with {\sl Select $\Rightarrow$ Undefine Groups} from the
alignment window menu. Note that tree partitioning will also remove any groups
and colourschemes on a view, so create a new view ([CTRL-T]) if you wish to
preserve these.

\begin{figure}
\begin{center}
\includegraphics[width=5in]{images/trees3.pdf}
\caption{{\bf Interactive Trees} The tree level cutoff can be used to designate
groups in Jalview.}
\label{trees2}
\end{center}
\end{figure}

%\subsubsection{Multiple Views and Input Data recovery from PCA and Tree Viewers}
% move to ch. 3 ?
%Both PCA and Tree viewers are linked analysis windows. This means that their selection and display are linked to a particular alignment, and control and reflect the selection state for a particular view.

\subsubsection{Recovering input Data for a Tree or PCA Plot Calculation}
\parbox[c]{5in}{
The {\sl File $\Rightarrow$ Input Data } option will open a new alignment window containing the original data used to calculate the tree or PCA plot (if available). This function is useful when a tree has been created and then the alignment subsequently changed. 
}
\parbox[c]{1.25in}{\centerline{\includegraphics[width=1.25in]{images/pca_fmenu.pdf}
}}

\subsubsection{Changing the associated View for a Tree or PCA Viewer}
\parbox[c]{4in}{
The {\sl View $\Rightarrow$ Associated Nodes With $\Rightarrow$ .. } submenu is shown when the viewer is associated with an alignment that is involved in multiple views. Selecting a different view does not affect the tree or PCA data, but will change the colouring and display of selected sequences in the display according to the colouring and selection state of the newly associated view. 
} \parbox[c]{3in}{\centerline{
\includegraphics[width=2.5in]{images/pca_vmenu.pdf} }}

\subsection{Tree Based Conservation Analysis}
\label{treeconsanaly}

Trees reflect the pattern of global sequence similarity exhibited by the
alignment, or region within the alignment, that was used for their calculation.
The Jalview tree viewer enables sequences to be partitioned into groups based
on the tree. This is done by clicking within the tree viewer window. Once subdivided, the
conservation between and within groups can be visually compared in order to
better understand the pattern of similarity revealed by the tree and the
variation within the clades partitioned by the grouping. The conservation based
colourschemes and the group associated conservation and consensus annotation
(enabled using the alignment window's {\sl View $\Rightarrow$ Autocalculated
Annotation $\Rightarrow$ Group Conservation} and {\sl Group Consensus} options)
can help when working with larger alignments.

\exercise{Trees}
{Ensure that you have at least 1G memory available in Jalview.

{\sl (Start with link:
\href{http://www.jalview.org/services/launchApp?jvm-max-heap=1G}{http://www.jalview.org/services/launchApp?jvm-max-heap=1G},
or in the Development section of the Jalview web site
(\href{http://www.jalview.org/development/development-builds}{http://www.jalview.org/development/development-builds})
in the table, go to ``latest official build'' row and ``Webstart'' column, click
on ``2G''.)}

\exstep{Open the alignment at \textsf{http://www.jalview.org/tutorial/alignment.fa}. 
Select {\sl Calculate $\Rightarrow$ Calculate Tree $\Rightarrow$ Neighbour
Joining Using BLOSUM62}. A tree window opens.} 
\exstep{Click on the
tree window, a cursor will appear. Note that placing this cursor divides the tree into a number of groups by colour.
Place the cursor to give about 4 groups.}
\exstep{In the alignment window, select
{\sl Calculate $\Rightarrow$ Sort $\Rightarrow$ By Tree Order $\Rightarrow$ Neighbour Joining Tree using BLOSUM62 from... }. The sequences are 
reordered to match the order in the tree and groups are formed implicitly.
Alternatively in the tree window, select {\sl View $\Rightarrow$ Sort Alignment
by Tree}.} 
\exstep{Select {\sl Calculate $\Rightarrow$ Calculate Tree
$\Rightarrow$ Neighbour Joining Using \% Identity}. A new tree window will
appear. The group colouring makes it easy to see the differences between the two
trees calculated by the different methods.}
\exstep{Select from sequence 2
column 60 to sequence 12 column 123. Select  {\sl Calculate $\Rightarrow$ Calculate Tree $\Rightarrow$ Neighbour Joining Using BLOSUM62}.
 A new tree window will appear. The tree contains 11 sequences. It has been coloured according to the already
 selected groups from the first tree and is calculated purely from the residues
 in the selection.}

Comparing the location of individual sequences between the three trees illustrates the importance of selecting appropriate regions of the 
alignment for the calculation of trees.

{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
}

\exercise{Pad Gaps in an Alignment}{
\exstep{Open the alignment at \textsf{http://www.jalview.org/tutorial/alignment.fa}. In alignment window, ensure that the {\sl Edit $\Rightarrow$
Pad Gaps } option is {\sl not} ticked, and insert one gap anywhere in the
alignment.}
\exstep{Select {\sl Calculate $\Rightarrow$ Calculate Tree $\Rightarrow$
Neighbour Joining Using BLOSUM62}.

A warning dialog box {\bf ``Sequences not aligned'' } appears because the sequences input to the tree calculation are of different lengths. }

\exstep{Select {\sl Edit $\Rightarrow$ tick Pad Gaps } and perform the
tree calculation again. This time a new tree should appear - because padding
gaps ensures all the sequences are the same length after editing.}
{\sl Pad Gaps } option
can be set in Preferences using
{\sl Tool $\Rightarrow$ Preference $\Rightarrow$ Editing}.

{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
}

\exercise{Tree Based Conservation Analysis}{
\label{consanalyexerc}
\exstep{Load the PF03460 PFAM seed alignment using the sequence fetcher. 
Select {\sl Colour $\Rightarrow$ Taylor $\Rightarrow$ By Conservation}, set {\sl Conservation} shading threshold at around 20. }
\exstep{Build a Neighbour joining tree using Select {\sl Calculate $\Rightarrow$ Calculate Tree $\Rightarrow$
Neighbour Joining Using BLOSUM62}.}
\exstep{Use the mouse cursor to select a point on the tree to partition the
alignment into several sections.}
\exstep {Select {\sl View $\Rightarrow$ Sort Alignment By Tree} option in the
tree window to re-order the sequences in the alignment using the calculated
tree.
Examine the variation in colouring between different groups of sequences in the alignment
window. }
\exstep {You may find it easier to browse the alignment if you first uncheck the
{\sl Annotations $\Rightarrow$ Show Annotations} option. Open the
Overview Window within the View menu to aid navigation.}

\exstep{Try changing the colourscheme of the residues in the alignment to
BLOSUM62 (whilst ensuring that {\sl Apply Colour to All Groups} is selected).}
{\sl Note: You may want to save the alignment and tree as a project file, since
it is used in the next set of exercises. }

{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
}


\subsection{Redundancy Removal}

The redundancy removal dialog box is opened using the {\sl Edit $\Rightarrow$ Remove Redundancy\ldots} option in the alignment menu. As its menu option placement suggests, this is actually an alignment editing function, but it is convenient to describe it here. The redundancy removal dialog box presents a percentage identity slider which sets the redundancy threshold. Aligned sequences which exhibit a percentage identity greater than the current threshold are highlighted in black. The [Remove] button can then be used to delete these sequences from the alignment as an edit operation\footnote{Which can usually be undone. A future version of Jalview may allow redundant sequences to be hidden, or represented by a chosen sequence, rather than deleted.}.
\begin{figure}
\begin{center}
\includegraphics[width=5.5in]{images/redundancy.pdf}
\end{center}
\label{removeredundancydialog}
\caption{The Redundancy Removal dialog box opened from the edit menu. Sequences that exceed the current percentage identity threshold and are to be removed are highlighted in black.}
\end{figure}


\subsection{Subdividing the Alignment According to Specific Mutations}

It is often necessary to explore variations in an alignment that may correlate
with mutations observed in a particular region; for example, sites exhibiting
single nucleotide polymorphism, or residues involved in substrate recognition in
an enzyme. One way to do this would be to calculate a tree using the specific
region, and subdivide it in order to partition the alignment.
However, calculating a tree can be slow for large alignments, and the tree may
be difficult to partition when complex mutation patterns are being analysed. The
{\sl Select $\Rightarrow$ Make groups for selection } function was introduced to
make this kind of analysis easier. When selected, it will use the characters in
the currently selected region to subdivide the alignment. For example, if a
single column is selected, then the alignment (or each group defined on the
alignment) will be divided into groups based on the residue or nucleotide found
at that position. These new groups are annotated with the characters in the
selected region, and Jalview's group based conservation analysis annotation and
colourschemes can then be used to reveal any associated pattern of sequence
variation across the whole alignment.


% These annotations can be hidden and deleted via the context menu linked to the
% annotation row; but they are only created on loading an alignment. If they are
% deleted then the alignment should be saved and then reloaded to restore them.
% Jalview provides a toggle to autocalculate a consensus sequence upon editing.
% This is normally selected by default, but can be turned off for large alignments {\sl via} the {\sl Calculate $\Rightarrow$ Autocalculate
% Consensus} menu option if the interface is too slow.

% \subsubsection{Group Associated Annotation}
% \label{groupassocannotation}
% Group associated consensus and conservation annotation rows reflect the
% sequence variation within a particular group. Their calculation is enabled
% by selecting the {\sl Group Conservation} or {\sl Group Consensus} options in
% the {\sl Annotation $\Rightarrow$ Autocalculated Annotation } submenu of the
% alignment window. 

% \subsubsection{Alignment and Group Sequence Logos}
% \label{seqlogos}

% The consensus annotation row that is shown below the alignment can be overlaid
% with a sequence logo that reflects the symbol distribution at each column of
% the alignment. Right click on the Consensus annotation row and select the {\sl
% Show Logo} option to display the Consensus profile for the group or alignment.
% Sequence logos can be enabled by default for all new alignments {\sl via} the
% Visual tab in the Jalview desktop's preferences dialog box.

\section{Pairwise Alignments}
Jalview can calculate optimal pairwise alignments between arbitrary 
sequences {\sl via} the {\sl Calculate $\Rightarrow$ Pairwise Alignments\ldots} menu option. 
Global alignments of all pairwise combinations of the selected sequences are performed and the results returned in a text box.



\exercise{Remove Redundant Sequences}{

\exstep{Using the alignment generated in the previous exercise (exercise
\ref{consanalyexerc}).
In the alignment window, you may need to deselect groups using Esc key.}

\exstep{In the {\sl Edit} menu select {\sl Remove Redundancy} to open the
Redundancy threshold selection dialog. Adjust the redundancy threshold value, start
at 50 and increase the value to 65. Sequences selected will change colour in the Sequence ID panel. Select ``Remove'' to
remove the sequences that are more than 65\% similar under this alignment.}

\exstep{From the tree window, select {\sl View $\Rightarrow$
Mark Unlinked Leaves} option, and note that the removed sequences are now prefixed with a * in the tree view.} \exstep{Use the [Undo] button in the Redundancy threshold selection dialog box
to recover the sequences. Note that the * symbols disappear from the tree display.}
\exstep{Experiment with the redundancy removal and observe the relationship between the percentage identity threshold and the pattern of unlinked nodes in the tree display.}
}

\exercise{Group Conservation Analysis}{
\exstep{Re-use or recreate the alignment and tree which you worked with in the
tree based conservation analysis exercise (exercise \ref{consanalyexerc}).} 
\exstep{In the {\sl View} menu in the alignment window, select {\sl New View} to
create a new view. Ensure the annotation panel is displayed ({\sl Show annotation} in {\sl Annotations} menu). Enable the
display of {\sl Group Consensus} option by checking {\sl Group Consensus} in the {\sl Annotation $\Rightarrow$
Autocalculated Annotation } submenu in the alignment window.}
\exstep{Displaying the sequence 
logos will make it easier to see the different residue populations within each
group. Activate the logo by right clicking on the Consensus annotation row to
open the context menu and select the {\sl Show Logo} option.} 
\exstep{In the column alignment ruler, select a column exhibiting about 50\%
conservation that lies within the central conserved region of the alignment.
(Column 74 is used in \href{https://youtu.be/m-PjynicXRg}{the Tree video}).} 
\exstep{Subdivide the alignment
according to this selection using {\sl Select $\Rightarrow$ Make groups for selection}.}
\exstep{Re-order the alignment according to the new groups that have been
defined by selecting {\sl Calculate $\Rightarrow$ Sort $\Rightarrow$
By Group}.

Click on the group annotation row IDs to select groups exhibiting a
specific mutation.}
\exstep{Select another column exhibiting about 50\% conservation
overall, and subdivide the alignment further. Note that the new groups
inherit the names of the original groups, allowing you to identify the
combination of mutations that resulted in the subdivision.}
\exstep{Clear the groups, and try to subdivide the alignment using two
non-adjacent columns.

{\sl Hint: You may need to hide the intervening columns before you can select
both of the columns that you wish to use to subdivide the alignment.}}
\exstep{Switch back to the original view, and experiment with subdividing
the tree groups made in the previous exercise.}
{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
}

\begin{figure}[]
\begin{center}
\includegraphics[width=4in]{images/pairwise.pdf}
\caption{{\bf Pairwise alignment of sequences.} Pairwise alignments of three selected sequences are shown in a textbox.}
\label{pairwise}
\end{center}
\end{figure}


% To review, Chapter \ref{featannot} describes the mechanisms provided by
% Jalview for interactive creation of sequence and alignment annotation, and how
% they can be displayed, imported and exported and used to reorder the alignment. Chapter
% \ref{featuresfromdb} discusses the retrieval of database references and
% establishment of sequence coordinate systems for the retrieval and display of
% features from databases and DAS annotation services.
% Chapter \ref{msaservices} describes how to use the range of multiple alignment
% programs provided by JABAWS, and Chapter \ref{aacons} introduces JABAWS AACon
% service for protein multiple alignment conservation analysis.
%  In Chapter \ref{alignanalysis}, you will find
% descriptions and exercises on building and displaying trees, PCA analysis,
% alignment redundancy removal, pairwise alignments and alignment conservation
% analysis. 
% Chapter \ref{wkwithstructure} introduces the structure visualization
% capabilities of Jalview.
% Chapter \ref{protsspredservices} explains how to perform protein secondary
% structure predictions with JPred, and JABAWS protein disorder prediction
% services are introduced in Chapter \ref{protdisorderpred}.
% Chapter \ref{workingwithnuc} describes functions and visualization techniques
% relevant to working with nucleotide sequences, coding region annotation and nucleotide
% sequence alignments.
% Chapter \ref{jvwebservices} introduces the various web based services
% available to Jalview users, and Chapter \ref{jabaservices} explains how to
% configure the Jalview Desktop for access to new JABAWS servers.


% and Section \ref{workingwithrna} covers the visualization,
% editing and analysis of RNA secondary structure.

\chapter{Working with 3D structures}
\label{3Dstructure}
\label{wkwithstructure}
Jalview facilitates the use of 3D structure data for the analysis of alignments
by providing a linked view of structures associated with the aligned sequences.
It also allows sequence, secondary structure and B-factor data to be imported
from structure files, and supports the use of the EMBL-EBI's SIFTS database to
construct accurate mappings between UniProt protein sequences and structures
retrieved from the PDB.

\section{Molecular graphics systems supported by Jalview}
Jalview can interactively view 3D structure using Jmol, a Java based molecular
viewing program\footnote{See the Jmol homepage \url{http://www.jmol.org} for
more information.} integrated with Jalview.\footnote{Earlier
versions of Jalview included MCView - a simple main chain structure viewer.
Structures are visualized as an alpha carbon trace and can be viewed, rotated
and coloured using the sequence alignment.} It also supports the use of UCSF
Chimera, a powerful molecular graphics system that needs separate installation.
Jalview can also read PDB and mmCIF format files directly to extract sequences
and secondary structure information, and retrieve records from the European
Protein Databank (PDBe) using the Sequence Fetcher (see \ref{fetchseq}).

\subsection{Configuring the default structure viewer}
\label{configuring3dviewer}
To configure which viewer is used when creating a new
structure view, open the Structures preferences window {\sl via} {\sl Tools $\Rightarrow$ Preferences\ldots} and
select either JMOL or CHIMERA as the default viewer. If you select Chimera,
Jalview will search for the installed program, and if it cannot be found,
you will be prompted to locate the Chimera binary, or alternately, open the UCSF
Chimera download page to obtain the software.

\section{Automatic Association of PDB Structures with Sequences}
Jalview will attempt to automatically determine which structures are associated
with a sequence via its ID, and any associated database references. To do this
for a particular sequence or the current selection, open the Sequence ID popup
menu and select {\sl View 3D Structure}, to open the 3D Structure Chooser. 
%(Figure\ref{auto}). 

When the structure chooser is first opened, if no database identifiers are
available, Jalview will automatically perform a database reference
retrieval (See \ref{fetchdbrefs}) to discover identifiers for the
sequences to use to search the PDB. This can take a
few seconds for each sequence and will be performed for all selected
sequences.\footnote{After this is done, you can can see the added database
references in a tool tip by mousing over the sequence ID. You can use the {\sl
View $\Rightarrow$ Sequence ID Tooltip $\Rightarrow$ Show Db References }
submenu option to enable or disable these data in the tooltip.}

Once the retrieval has finished, the structure chooser dialog will show any
available PDB entries for the selected sequences.

% 
% \begin{figure}[htbp]
% \begin{center}
% %TODO fix formatting
% \begin{center} 
% \includegraphics[width=3.5in]{images/pdbstructurechooser.pdf}
% \end{center}
% 
% 
% \caption{{\bf The PDB Structure Chooser dialog.} }
% \label{auto}
% \end{center}
% \end{figure}

\subsection{Drag-and-Drop Association of PDB Files with Sequences by Filename
Match}
\label{multipdbfileassoc}
If you have PDB files stored on your computer named the same way as the
sequences in the alignment, then you can drag them from their location on the
file browser onto an alignment window. Jalview will search the alignment for
sequences with IDs that match any of the files, and offer a dialog like the one
in Figure \ref{multipdbfileassocfig}.

If no associations are made, then sequences extracted
from the structure will be simply added to the alignment. However, if only
some of the PDB files are associated, Jalview will raise another dialog box
giving you the option to add any remaining sequences from the PDB structure files not present in
the alignment. This allows you to easily decorate sequences in a newly imported
alignment with any corresponding structures you've already collected in a directory
accessible from your computer.\footnote{We plan to extend this facility in
future so Jalview will automatically search for PDB files matching your
sequence within a local directory. Check out 
\href{http://issues.jalview.org/browse/JAL-801}{Jalview issue 801}}

After associating sequences with PDB files, you can view the PDB structures by
opening the Sequence ID popup
menu and selecting {\sl View 3D Structure}. The PDB files you loaded will be
shown in the {\bf Cached Structures} view, after selecting it from the drop down
menu in the dialog box. 

% there is no mention of the other footnote (#3) that appears saying: Tip: The sequence ID tooltip can often become large for heavily cross-referenced sequence IDs. Use the ...
% JBP: yes there is - under 'Discovery of ' subsection.
\begin{figure}[htbp]
\begin{center}
\includegraphics[]{images/pdbdragdropassoc.pdf}

\caption{{\bf Associating PDB files with sequences by drag-and-drop.} Dragging
PDB files onto an alignment of sequences with names matching the dragged files
names (A), results in a dialog box (B) that gives the option to associate each
file with any sequences with matching IDs. }
\label{multipdbfileassocfig}
\end{center}
\end{figure}


\section{Viewing Structures}
\label{structurechooser}
The structure viewer is launched via the Sequence ID context
menu. To view structures associated with a sequence or a selected set of
sequences in the alignment, simply right click the mouse to open the context
menu, and select {\sl 3D Structure data \ldots} to open the Structure Chooser
dialog box. 

If any of
the {\bf currently selected} sequences have structures in the PDB, 
they will appear in the Structure Chooser dialog box. The structures can be ranked by
different parameters, but are by default ordered according to their PDB
quality score. 

To view one or more structures, simply click {\sl
View} to open a structure viewer containing the structures selected in the
dialog. If several structures were picked, these will be shown
superposed according to the alignment.
You may find Jalview has already picked the best structure - using one of the
criteria shown in the dropdown menu (e.g. 'Best Quality', which is picked by
default). However, you are free to select your own.

The structure(s) to be displayed will be downloaded or loaded from
the local file system, and shown as a ribbon diagram coloured according to the
associated sequence in the current alignment view (Figure \ref{structure}
(right)). The structure can be rotated by clicking and dragging in the structure
window. The structure can be zoomed using the mouse scroll wheel or by
[SHIFT]-dragging the structure.

Moving the mouse cursor over a sequence to which the structure is linked in the
alignment view highlights the respective residue's sidechain atoms. The
sidechain highlight may be obscured by other parts of the molecule. Similarly,
moving the cursor over the structure shows a tooltip and highlights the
corresponding residue in the alignment. Clicking the alpha carbon or phosphorous
backbone atom will toggle the highlight and residue label on and off. Often, the
position highlighted in the sequence may not be in the visible portion of the
current alignment view and the sliders will scroll automatically to show the
position. If the alignment window's {\sl View $\Rightarrow$ Automatic Scrolling
} option is not selected, however, then the automatic adjustment will be
disabled for the current view.

\begin{figure}[htbp]
\begin{center}
\parbox{4in}{
{\centering 
\begin{center}
\includegraphics[width=4in]{images/structure1.pdf}
\end{center}
}
}
\parbox{2.2in}{
{\centering 
\begin{center}
\includegraphics[width=2.2in]{images/structure2.pdf}
\end{center}
}
}
\caption{{\bf Structure visualization} Structure viewers are launched from
the 3D Structure chooser dialog (left). Jalview shows the displayed structures
coloured according the alignment view (right). }
\label{structure}
\end{center}
\end{figure}

\subsection{Customising Structure Display}

Structure display can be modified using the {\sl Colour} and {\sl View} menus
in the structure viewer. The background colour can be modified by selecting the
{\sl Colours $\Rightarrow$ Background Colour\ldots} option.

By default, the structure will be coloured in the same way as the associated
sequence(s) in the alignment view from which it was launched. The structure can
be coloured independently of the sequence by selecting an appropriate colour
scheme from the {\sl Colours} menu. It can be coloured according to the
alignment using the {\sl Colours $\Rightarrow$ By Sequence } option. The image
in the structure viewer can be saved as an EPS or PNG with the {\sl File
$\Rightarrow$ Save As $\Rightarrow$ \ldots} submenu, which also allows the raw
data to be saved as PDB format. The mapping between the structure and the
sequence (how well and which parts of the structure relate to the sequence) can
be viewed with the {\sl File $\Rightarrow$ View Mapping} menu option.

\subsubsection{Using the Jmol Visualization Interface }

Jmol has a comprehensive set of selection and visualization functions that are
accessed from the Jmol popup menu (by right-clicking in the Jmol window or by
clicking the Jmol logo). Molecule colour and rendering style can be manipulated,
and distance measurements and molecular surfaces can be added to the view. It
also has its own ``Rasmol\footnote{See \url{http://www.rasmol.org}}-like'' scripting
language, which is described elsewhere\footnote{Jmol Wiki:
\url{http://wiki.jmol.org/index.php/Scripting}

Jmol Scripting reference:
\url{http://www.stolaf.edu/academics/chemapps/jmol/docs/}}. Jalview utilises the
scripting language to interact with Jmol and to store the state of a Jmol
visualization within Jalview archives, in addition to the PDB data file
originally loaded or retrieved by Jalview. To access the Jmol scripting
environment directly, use the {\sl Jmol $\Rightarrow$ Console} menu option.

If you would prefer to use Jmol to manage structure colours, then select the
{\sl Colours $\Rightarrow$ Colour with Jmol} option. This will disable any
automatic application of colour schemes when new structure data is added, or
when associated alignment views are modified.

\exercise{Viewing Structures with the integrated Jmol
Viewer}{\label{viewingstructex} \exstep{Load the alignment at
\textsf{http://www.jalview.org/examples/exampleFile.jar}.}
\exstep{Right-click on the
sequence ID label of {\sl FER1\_SPIOL} to open
the ID popup menu and select {\sl 3D Structure}. After a short pause, a
Structure Chooser dialog will open for the sequence, listing available
structure data from the PDB. Select { \sl 1A70} from the list and click {\sl
View}.

{\sl The Structure Chooser dialog presents available PDB structures
by querying the EMBL-EBI's PDBe web API. Extra information can be
including in this window by checking boxes in the columns of the ``Customise Displayed Options'' tab}.
% JBP Note: Bug JAL-1238 needs to be fixed ASAP
}
\exstep{By default the Jmol
structure viewer opens in the Jalview desktop. Rotate the molecule by clicking
and dragging in the structure viewing box.
Zoom with the mouse scroll wheel. } 
\exstep{Roll the
mouse cursor along the {\sl FER1\_SPIOL} sequence in the alignment.
Note that if a residue in the sequence maps to one in the structure, a label
will appear next to that residue in the structure viewer.}
\exstep{Move the mouse over the structure. In the Jmol viewer, placing the mouse over a
part of the structure will bring up a tool tip indicating the name and number of that residue.
In the alignment window, the corresponding residue in the sequence is
highlighted in black.}
\exstep{Clicking the alpha carbon toggles the highlight and residue label on and
off.
Try this by clicking on a set of three or four adjacent residues so that the labels are persistent, then finding where they are in the sequence. }
\exstep{In the structure viewer menu, select {\sl Colours $\Rightarrow$ Background
Colour\ldots} and choose a suitable colour.
Press {\sl OK} to apply this.}
\exstep{Select {\sl File $\Rightarrow$ Save As $\Rightarrow$ PNG} and save the
image. On your computer, view this with a suitable program. } 
\exstep{Select
{\sl File $\Rightarrow$ View Mapping} from the structure viewer menu.
A new window opens showing the residue by residue alignment between the sequence and the structure.} 
\exstep{Select {\sl File $\Rightarrow$ Save $\Rightarrow$ PDB file} and choose a new filename to save the PDB file. 
Once the file is saved, open the location in your file browser (or explorer
window) and drag the PDB file that you just saved on to the Jalview desktop (or load it from the {\sl Jalview Desktop $\Rightarrow$ Input Alignment $\Rightarrow$ From File } menu). 
Verify that you can open and view the associated structure from the sequence ID
context menu's {\sl 3D Structure } submenu in the new alignment window.}

\exstep{In the Jmol window, right click on the structure window and explore the
menu options. Try to change the style of molecular display - for example by
using the {\sl Jmol $\Rightarrow$ Select (n) $\Rightarrow$ All} command (where {\sl n} is the number of residues selected), and then the {\sl Jmol $\Rightarrow$ Style $\Rightarrow$ Scheme $\Rightarrow$ Ball and Stick} command.} 
\exstep{In the alignment window, use the {\sl File $\Rightarrow$ Save As.. }
function to save the alignment as a Jalview Project. Now close the alignment and the structure view, and load the project file you just saved.
Verify that the Jmol display is as it was when you just saved the file.}
{\bf See the video at:
\url{http://www.jalview.org/training/Training-Videos}.}
}

\exercise{Setting Chimera as the default 3D Structure Viewer}{\label{viewingchimera} 
Jalview supports molecular structure
visualization using both Jmol and Chimera 3D viewers. Jmol is the default
viewer, however Chimera can be set up as the default choice from Preferences.

\exstep{First, Chimera must be downloaded and installed on the computer.
Chimera program is available on the UCSF web site \textsf{https://www.cgl.ucsf.edu/chimera/download.html}.}
\exstep{In the desktop menu, select {\sl Tool  $\Rightarrow$ Preferences}. In
the ``{\sl
Structure}'' tab set {\sl Default structure viewer} as {\sl
Chimera}; then click {\sl OK}.} 
\exstep{Close the Jalview program, from the
{\sl Desktop menu} select {\sl Jalview $\Rightarrow$ Quit Jalview}. Then reopen
Jalview, Chimera should open as the default viewer.}
{\sl Note: The Jmol structure viewer sits within the Jalview desktop. However
the Chimera structure viewer sits outside the Jalview desktop and a Chimera
view window sits inside the Jalview desktop.}

{\bf See the video at: \url{http://www.jalview.org/training/Training-Videos}.} }

\subsection{Superimposing Structures}
\label{superposestructs}
Many comparative biomolecular analysis investigations aim to determine if the
biochemical properties of a given molecule are significantly different to its
homologues. When structure data is available, comparing the shapes of molecules
by superimposing them enables substructure that may impart different behaviour
to be quickly identified. The identification of optimal 3D superposition
involves aligning 3D data rather than sequence symbols, but the result can
still be represented as a sequence alignment, where columns indicate positions
in each molecule that should be superposed to recreate the optimal 3D alignment.

Jalview can employ Jmol's 3D fitting routines\footnote{See
\href{http://chemapps.stolaf.edu/jmol/docs/?ver=12.2$\#$compare}{http://chemapps.stolaf.edu/jmol/docs/?ver=12.2$\#$compare}
for more information.} to recreate 3D structure superpositions based on the
correspondences defined by one or more sequence alignments involving structures shown in the Jmol display. Superposition based on the currently displayed alignment view
 happens automatically if a
structure is added to an existing Jmol display using 
the {\sl 3D Structure } option in the Sequence ID popup menu to open the
Structure Chooser dialog box.
Select the structures required and select {\sl View}. A new Jmol view
opens containing superposed structures if the current selection contains two or more sequences with associated
structures.

\subsubsection{Obtaining the RMSD for a Superposition}
The RMSD (Root Mean Square Deviation) is a measure of how similar the structures
are when they are superimposed. Figure \ref{mstrucsuperposition} shows a
superposition created during the course of Exercise \ref{superpositionex}. The
parts of each molecule used to construct the superposition are rendered using
the cartoon style, with other parts of the molecule drawn in wireframe. The Jmol
console, which has been opened after the superposition was performed, shows the
RMSD report for the superposition.
Full information about the superposition is also reported on the Jalview
console.\footnote{The Jalview Java Console is opened from {\sl Tools
$\Rightarrow$ Java Console} option in the Desktop's menu bar} This output also
includes the precise atom pairs used to superpose structures.

\subsubsection{Choosing which part of the Alignment is used for Structural
Superposition} Jalview uses the visible part of each alignment view to define
which parts of each molecule are to be superimposed. Hiding a column in a view
used for superposition will remove that correspondence from the set, and will
exclude it from the superposition and RMSD calculation.
This allows the selection of specific parts of the alignment to be used for
superposition. Only columns that define a complete set of correspondences for
all structures will be used for structural superposition, and as a consequence,
the RMSD values generated for each pair of structures superimposed can be
directly compared.

In order to recompute a superposition after changing a view or editing the
alignment, select the {\sl Jmol $\Rightarrow$ Align Structures} menu option.
The {\sl Jmol $\Rightarrow$ Superpose with ..} submenu allows you to choose which of the
associated alignments and views are to be used to create the set of
correspondences. This menu is useful when composing complex superpositions
involving multi-domain and multi-chain complexes, when correspondences may be
defined by more than one alignment.

Note that these menu options appear when you have two or more structures in one Jmol viewer.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=5.5in]{images/fdxsuperposition.pdf}
\caption{{\bf Superposition of two ferredoxin structures.} The alignment on the
left was used by Jalview to superpose structures associated with the
FER1\_SPIOL and FER1\_MAIZE sequences in the alignment. Parts of each structure
used for superposition are rendered as a cartoon, the remainder rendered in
wireframe. The RMSD between corresponding positions in the structures before and
after the superposition is shown in the Jmol console.}
\label{mstrucsuperposition}
\end{center}
\end{figure}

\subsection{Colouring Structure Data Associated with Multiple Alignments and
Views} Normally, the original view from which a particular structure view was
opened will be the one used to colour structure data. If alignments involving
sequences associated with structure data shown in a Jmol have multiple views, Jalview gives you full control
over which alignment, or alignment view, is used to colour the structure
display. Sequence-structure colouring associations are
changed {\sl via} the {\sl View $\Rightarrow$ Colour by ..} menu, which lists all
views associated with data shown in the embedded Jmol view. A tick is shown beside
views currently used as colouring source, and moving the
mouse over each view will bring it to the front of the alignment display,
allowing you to browse available colour sources prior to selecting one. If the
{\sl Select many views} option is selected, then multiple views can be selected as sources for colouring the
structure data. {\sl Invert selection} and {\sl Select all views} options are also provided to quickly change between multi-view selections.

Note that the {\sl Select many views} option is useful if you have different
views that colour different areas or domains of the alignment. This option is
further explored in Section \ref{complexstructurecolours}.


\exercise{Aligning Structures using the Ferredoxin
Sequence Alignment}{\label{superpositionex}

\exstep{Continue with the Jalview project created in exercise
\ref{viewingstructex}}

\exstep{Open the 3D Structure chooser dialog from the popup menu for FER1\_SPIOL
by right-clicking its ID (CMD-click on Macs), and selecting {\sl $\Rightarrow$
3D Structure Data \ldots } }

\exstep{Pick 1A70 from the Structure Chooser dialog, and click the {\bf View}
button. Jalview will give you the option of aligning the
structure to the one already open. To superimpose the structure associated with
FER1\_MAIZE with the one associated with FER1\_SPIOL, press {\sl Yes}.

{\sl The Jmol view should update to show both structures, and one will be
moved on to the other. If this doesn't happen, use the Align function in the
Jmol submenu}.
}

\exstep{Create a new view on the alignment, and hide all but columns 121
through to 132 (you can do this via {\sl View $\Rightarrow$ Hide $\Rightarrow$
All but selected region}).}
\exstep{Select the newly created view in the {\sl Jmol $\Rightarrow$ Superpose
With } submenu, and then recompute the superposition with {\sl Jmol
$\Rightarrow$ Align Structures}.

{\sl Note how the molecules shift position when superposed with only a small
region of the alignment.}}

\exstep{Compare RMSDs obtained when superimposing molecules with
columns 121-132 and with the whole alignment.}

\exstep{The RMSD report can be
viewed by right clicking the mouse on Jmol window, and select {\sl
Console} from the menu (if nothing is shown, recompute the superposition after
displaying the console).

Which view do you think give the best 3D superposition, and why ?} }

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=5.5in]{images/mviewstructurecol.pdf}
\caption{{\bf Choosing a different view for colouring a structure display}
Browsing the {\sl View $\Rightarrow$ Colour by ..} menu provides full control
of which alignment view is used to colour structures when the {\sl Colours
$\Rightarrow$ By Sequence} option is selected.}
\label{mviewstructurecol}
\end{center}
\end{figure}

\subsubsection{Colouring Complexes}
\label{complexstructurecolours}
The ability to control which multiple alignment view is used to colour
structural data is essential when working with data relating to
multidomain biomolecules and complexes. 

In these situations, each chain identified in the structure may have a different
evolutionary history, and a complete picture of functional variation can
only be gained by integrating data from different alignments on the same
structure view. An example of this is shown in Figure
\ref{mviewalcomplex}, based on data from Song et. al.\footnote{Structure of
DNMT1-DNA Complex Reveals a Role for Autoinhibition in Maintenance DNA Methylation. Jikui Song, Olga Rechkoblit, Timothy H. Bestor, and Dinshaw J. Patel.
{\sl Science} 2011 {\bf 331} 1036-1040
\href{http://www.sciencemag.org/content/331/6020/1036}{DOI:10.1126/science.1195380}}

\begin{figure}[htbp]
\begin{center}
\includegraphics[]{images/mchainstructureview.pdf}
\caption{{\bf The biological assembly of Mouse DNA Methyltransferase-1 coloured
by Pfam alignments for its major domains} Alignments for each domain within the
Uniprot sequence DNMT1\_MOUSE have been used to visualise sequence conservation
in each component of this protein-DNA complex. Instructions for recreating this figure are given in exercise \ref{dnmtcomplexex}. }
\label{mviewalcomplex}
\end{center}
\end{figure}

\exercise{Colouring a Protein Complex to Explore Domain-Domain
Interfaces}{\label{dnmtcomplexex}

\exstep{Download the PDB file at
\textsf{\url{http://www.jalview.org/tutorial/DNMT1\_MOUSE.pdb}} to your desktop. 
This is the biological unit for PDB ID 3pt6, as identified by the PDBe's PISA
server.}
\exstep{Launch the Jalview desktop and ensure you have at least 1G of
free memory available.

{\sl See section \ref{memorylimits} for how to do this or click the following
link:

\url{http://www.jalview.org/services/launchApp?jvm-max-heap=2G} }}

\exstep{Retrieve the following PFAM alignments from the {\bf PFAM (full)} source
:
PF02008 PF01426 PF00145 (enter all three - they
will each be retrieved into their own alignment window).}

\exstep{Drag the URL or file of the structure you
downloaded in step 1 onto one of the alignments to associate it with the mouse sequence in that Pfam domain family.}

\exstep{Use the Find dialog to locate every DNMT1\_MOUSE sequence in the
alignment and for each one, open the Structure Chooser via the ID popup
menu ({\sl $\Rightarrow$ 3D Structure Data }. Select the DNMT1\_MOUSE.pdb
structure from the `Cached Structures' view, and click {\bf View}.

{\em Part of the newly opened structure will be coloured the same way as
the associated DNMT1\_MOUSE sequence is in the alignment view.}

{\bf WARNING: do not select all sequences and open the Structure Chooser
!} {\em This will cause Jalview to attempt to discover all structures for
sequences in the alignment.}
}
\exstep{Repeat the previous two steps for each of the other
alignments. In each case, after selecting the DNMT1\_MOUSE.pdb structure and
hitting the `View' button on the Structure Chooser dialog, Jalview will ask if you wish to create
a new Jmol view. Respond {\bf `Yes'} each time. This will ensure ensure each sequence
fragment is associated with the {\bf same} Jmol view. }

\exstep{Pick a different
colourscheme for each alignment, and use the {\sl Colour by ..} submenu to
ensure they are all used to colour the complex shown in the Jmol window.

{\sl The different shading schemes will allow regions of strong physicochemical conservation are
highlighted on the domains in the structure.}
}

\exstep{The final step needed to reproduce the shading in Figure
\ref{mviewalcomplex} is to use the {\sl Colour $\Rightarrow$ By
Annotation\ldots } option in each alignment window to shade the alignment by the
{\bf Conservation} annotation row (introduced in section
\ref{colourbyannotation}).

Ensure that you first disable the {\sl View $\Rightarrow$ Show Features} menu
option, or you may not see any colour changes in the associated structure.

{\sl Examine the regions strongly coloured at the interfaces betweeen each
protein domain, and the DNA binding region. What do you think these patterns
mean ? } }
\exstep{Save your work as a Jalview project and verify that it can be opened
again by starting another Jalview Desktop instance, and dragging the saved
project into the desktop window.}

% {\sl Note: This exercise relies on new features introduced in Jalview 2.7. If
% you notice any strange behaviour when trying out this exercise, it may be a
% bug (see
% \href{http://issues.jalview.org/browse/JAL-1008}{http://issues.jalview.org/browse/JAL-1008}
% for one relating to highlighting of positions in the alignment window).}
}

% TODO
\chapter{Protein sequence analysis and structure prediction}
\label{proteinprediction}

Many of Jalview's sequence feature and annotation capabilities were developed to
allow the results of sequence based protein structure prediction methods to be
visualised and explored. This chapter introduces services integrated with the
Jalview Desktop for predicting protein secondary structure and protein disorder.

\section{Protein Secondary Structure Prediction}
\label{protsspredservices}
Protein secondary structure prediction is performed using the
Jpred\footnote{{\sl ``The Jpred 3 Secondary Structure Prediction Server''} Cole,
C., Barber, J. D. and Barton, G. J. (2008) {\sl Nucleic Acids Research} {\bf
36}, (Web Server Issue) W197-W201

{\sl ``Jpred: A Consensus Secondary Structure Prediction Server''} Cuff, J. A.,
Clamp, M. E., Siddiqui, A. S., Finlay, M. and Barton, G. J. (1998) {\sl
Bioinformatics} {\bf 14}, 892-893} server at the University of
Dundee\footnote{http://www.compbio.dundee.ac.uk/www-jpred/}. The behaviour of
this calculation depends on the current selection:
\begin{list}{$\circ$}{}
\item If nothing is selected, Jalview will check the length of each alignment row to determine if the visible sequences in the view are aligned.
\begin{list}{-}{}
              \item If all rows are the same length (often due to the
              application of the {\sl Edit $\Rightarrow$ Pad Gaps} option), then
              a JPred prediction will be run for the first sequence in the
              alignment, using the current alignment as the profile to use for prediction.
              \item  Otherwise, just the first sequence will be submitted for a
              full JPred prediction.
\end{list}
\item If just one sequence (or a region in one sequence) has been selected, it
will be submitted to the automatic JPred prediction server for homolog detection
and prediction.
\item If a set of sequences are selected, and they appear to be aligned using
the same criteria as above, then the alignment will be used for a JPred
prediction on the first sequence in the set (that is, the one that appears first in the alignment window).
\end{list}


\begin{figure}[htbp]
\begin{center}
\includegraphics[width=2.25in]{images/jpred1.pdf}
\includegraphics[width=3in]{images/jpred2.pdf}
\caption{{\bf Secondary Structure Prediction} Status (left) and results (right)
windows for JPred predictions. }
\label{jpred}
\end{center}
\end{figure}


Jpred is launched in the same way as the other web services. Select {\sl Web
Service $\Rightarrow$ Secondary Structure Prediction $\Rightarrow$ JPred
Secondary Structure Prediction}\footnote{JNet is the Neural Network based
secondary structure prediction method that the JPred server uses.} from the
alignment window menu (Figure \ref{jpred}).
A status window opens to inform you of the progress of the job. Upon completion, a new alignment window opens and the Jpred
predictions are included as annotations. Consult the Jpred documentation for
information on interpreting these results.

\subsection{Hidden Columns and JPred Predictions}
\label{hcoljnet}
Hidden columns can be used to exclude parts of a sequence or profile from the
input sent to the JNet service. For instance, if a sequence is known to include
a large loop insertion, hiding that section prior to submitting the JNet
prediction can produce different results. In some cases, these secondary
structure predictions can be more reliable for sequence on either side of the
insertion\footnote{This, of course, cannot be guaranteed.}. Prediction results
returned from the service will be mapped back onto the visible parts of the
sequence, to ensure a single frame of reference is maintained in your analysis.


\exercise{Secondary Structure Prediction}{
\label{secstrpredex}

{\sl Note: The annotation panel can get quite busy during this exercise. Try
hiding some annotations rows by right clicking
the mouse in the annotation label panel and select the ``Hide this row'' option.
The Annotations dropdown menu on the alignment wndow also provides options for
reording and hiding autocalculated and sequence associated annotation. }

\exstep{ Open the alignment at \url{http://www.jalview.org/tutorial/alignment.fa}. Select the sequence {\sl FER\_MESCR} by 
clicking on the sequence ID. Then select {\sl Web Service $\Rightarrow$
Secondary Structure Prediction $\Rightarrow$ JPred Secondary Structure
Prediction} from the alignment window menu. A status window will appear and after some time (about 2-4 min) a new window with the JPred prediction will appear.
Note that the number of sequences in the results window is many more than in the original alignment as 
JPred performs a PSI-BLAST search to expand the prediction dataset. The results
from the prediction are visible in the annotation panel. JPred secondary
structure prediction annotations are examples of sequence-associated alignment annotation. }
% TODO: check how long this takes - about 2 mins once it gets on the cluster.
\exstep{
Select a different sequence and perform a JPred prediction in the same way.
There will probably be minor differences in the predictions.
}
\exstep{
Select the sequence used in the second sequence prediction by clicking on its
name in the sequence ID panel, and copy {\sl ([CTRL] or [CMD]-C)} and then
paste it {\sl [CTRL] or [CMD]-V)} into the first prediction window.  You
can now compare the two predictions as the annotations associated with the
sequence has also been copied across.
% which is described in Section \ref{seqassocannot} below.
}
\exstep{
Select and hide some columns in one of the alignment profiles that were returned
from the JNet service, and then submit the profile for prediction again.
}
\exstep{
When you get the result, verify that the prediction has not been made for the
hidden parts of the profile (by clicking the mouse on column ruler and right click to open the
context menu and select {\sl Reveal All}), and that the JPred reliability scores
differ from the prediction made on the full profile.
}
\exstep{
In the original alignment that you loaded in step 1, select {\bf all}
sequences, then open the {\sl Sequence ID $\Rightarrow$ Selection } submenu
by right clicking the mouse to open the context menu, and select the {\sl Add
Reference Annotation} option.

{\bf All} the JPred predictions for the sequences will now be visible in the
original alignment window.}

{\bf Homework:} Go back to the last step of exercise \ref{annotatingalignex} and
follow the instructions to view the Jalview annotations file created from the annotations
generated by the JPred server for your sequence.}

\section{Protein Disorder Prediction}
\label{protdisorderpred}

Disordered regions in proteins were classically thought to correspond to
``linkers'' between distinct protein domains, but disorder can also play a role in
function. The {\sl Web Service $\Rightarrow$ Disorder} menu in the alignment window
allows access to protein disorder prediction services provided by the configured
JABAWS servers. 

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=5in]{images/disorderpredannot.pdf}
\caption{{\bf Annotation rows for several disorder predictions on a sequence}. A
zoomed out view of a prediction for a single sequence. The sequence is shaded to highlight disordered regions (brown and grey), and the line plots below the Sequence show the raw scores for various disorder predictors. Horizontal lines on each graph mark the level at which disorder predictions become significant. }
\label{alignmentdisorderannot}
\end{center}
\end{figure}

\subsection{Disorder Prediction Results}
Each service operates on sequences in the alignment to identify regions likely
to be unstructured or flexible, or alternately, fold to form globular domains.
As a consequence, disorder predictor results include both sequence features and
sequence associated alignment annotation rows. Section \ref{featannot} describes
the manipulation and display of these data in detail, and Figure
\ref{alignmentdisorder} demonstrates how sequence feature shading and
thresholding (described in Section \ref{featureschemes}) can be used to
highlight differences in disorder prediction across aligned sequences.

\begin{figure}[htbp]
\begin{center}
\includegraphics[width=5in]{images/disorderpred.pdf}
\caption{{\bf Shading alignment by sequence disorder}. Alignment of Interleukin IV homologs coloured with Blosum62 with protein disorder prediction sequence features overlaid, shaded according to their score. Borderline disordered regions appear white, reliable predictions are either Green or Brown depending on the type of disorder prediction. }
\label{alignmentdisorder}
\end{center}
\end{figure}

\subsection{Navigating Large Sets of Disorder Predictions}

Figure \ref{alignmentdisorderannot} shows a single sequence annotated with
a range of disorder predictions. Disorder prediction annotation rows are
associated with a sequence in the same way as secondary structure prediction
results. When browsing an alignment containing large numbers of disorder
prediction annotation rows, clicking on the annotation row label will highlight
the associated sequence in the alignment display, and double clicking will
select that sequence.

\subsection{Disorder Predictors provided by JABAWS 2.0}
For full details of each predictor and the results that Jalview can display,
please consult
\href{http://www.jalview.org/help/html/webServices/proteinDisorder.html}{Jalview's
protein disorder service documentation}. Short descriptions of the methods provided in JABAWS 2.0 are given below:

\subsubsection{DisEMBL}
\href{http://dis.embl.de/}{DisEMBL (Linding et al., 2003)} is a set of machine-learning based predictors trained to
recognise disorder-related annotation found on PDB structures.

\textbf{COILS} Predicts
loops/coils according to DSSP
definitions\footnote{DSSP Classifications of secondary structure are: $\alpha$-helix (H), 310-helix (G), $\beta$-strand (E)
are ordered, and all other states ($\beta$-bridge (B), $\beta$-turn (T), bend (S),
$\pi$-helix (I), and coil (C)) considered loops or coils.}. Features mark range(s) of
residues predicted as loops/coils, and annotation row gives raw value
for each residue. Value over 0.516 indicates loop/coil.

\textbf{HOTLOOPS} constitute a refined subset of \textbf{COILS}, namely those loops with
a high degree of mobility as determined from C$\alpha$ temperature factors (B
factors). It follows that highly dynamic loops should be considered
protein disorder. Features mark range(s) of residues predicted to
be hot loops and annotation row gives raw value for each
residue. Values over 0.6 indicates hot loop.

\textbf{REMARK465} ``Missing
coordinates in X-ray structure as defined by remark465 entries in PDB.
Nonassigned electron densities most often reflect intrinsic disorder,
and have been used early on in disorder prediction.'' Features give
range(s) of residues predicted as disordered, and annotation rows gives
raw value for each residue. Values over 0.1204 indicates disorder.

\subsubsection{RONN {\sl a.k.a.} Regional Order Neural Network}
\href{http://www.strubi.ox.ac.uk/RONN}{RONN} employs an approach
known as the `bio-basis' method to predict regions of disorder in
sequences based on their local similarity with a gold-standard set of
disordered protein sequences. It yields a set of disorder prediction
scores, which are shown as sequence annotation below the alignment.

\textbf{JRonn}\footnote{JRonn denotes the score for this server because JABAWS
runs a Java port of RONN developed by Peter Troshin and distributed as
part of \href{http://www.biojava.org/}{Biojava 3}} Annotation Row gives RONN score for each residue in
the sequence. Scores above 0.5 identify regions of the protein likely
to be disordered.

\subsubsection{IUPred}
\href{http://iupred.enzim.hu/Help.php}{IUPred} employs
an empirical model to estimate likely regions of disorder. There are
three different prediction types offered, each using different
parameters optimized for slightly different applications. It provides
raw scores based on two models for predicting regions of `long
disorder' and `short disorder'. A third predictor identifies regions
likely to form structured domains.

\textbf{Long disorder} Annotation rows predict
context-independent global disorder that encompasses at least 30
consecutive residues of predicted disorder. A 100 residue
window is used for calculation. Values above 0.5 indicates the residue is
intrinsically disordered.

\textbf{Short disorder} Annotation rows predict for short, (and
probably) context-dependent, disordered regions, such as missing
residues in the X-ray structure of an otherwise globular protein.
Employs a 25 residue window for calculation, and includes adjustment
parameter for chain termini which favors disorder prediction at the
ends. Values above 0.5 indicate short-range disorder.

\textbf{Structured domains} are marked with sequence Features. These highlight
likely globular domains useful for structure genomics investigation. Post-analysis of disordered region profile to find continuous regions
confidently predicted to be ordered. Neighbouring regions close to
each other are merged, while regions shorter than the minimal domain
size of at least 30 residues are ignored.

\subsubsection{GLOBPLOT}
\href{http://globplot.embl.de/}{GLOBPLOT} defines regions of
globularity or natively unstructured regions based on a running sum of
the propensity of residues to be structured or unstructured. The
propensity is calculated based on the probability of each amino acid
being observed within well defined regions of secondary structure or
within regions of random coil. The initial signal is smoothed with a
Savitzky-Golay filter, and its first order derivative
computed. Residues for which the first order derivative is positive
are designated as natively unstructured, whereas those with negative
values are structured.

{\bf Disordered region} sequence features are created marking mark range(s) of residues with positive first order derivatives, and 
\textbf{Globular Domain} features mark long stretches of order. \textbf{Dydx} annotation rows give the first order derivative of smoothed score. Values above 0 indicates
residue is disordered. 

\textbf{Smoothed Score and Raw Score} annotation rows give the smoothed and raw scores used to create the differential signal that
indicates the presence of unstructured regions. These are hidden
by default, but can be shown by right-clicking on the alignment
annotation panel and selecting \textbf{Show hidden annotation}.

\exercise{Protein Disorder Prediction}{
%\label{protdispredex}
{\sl Before starting this exercise, make sure you enable the \protect{`Add
Temperature Factor'} option in your {\bf Structures} preferences. }

\exstep{Open the alignment at:
\url{http://www.jalview.org/tutorial/interleukin7.fa}. } 

\exstep{Run the DisEMBL disorder predictor {\slvia} the {\slWeb Service
$\Rightarrow$ Disorder Prediction } submenu.}

\exstep{Select all the sequences, and open the Structure Chooser via the {\sl
Sequence ID $\Rightarrow$ 3D Structure Data\ldots } popup menu. Hit the
{\bf View} button to retrieve and show all PDB structures for the sequences.}

\exstep{Compare the disorder predictions to the structure data by mapping any
available temperature factors to the alignment {\sl via} the {\sl Sequence ID
Popup $\Rightarrow$ Selection $\Rightarrow$ Add reference annotation} option.}

\exstep{Apply the IUPred disorder prediction method. Use the {\sl Per
sequence option} in the {\sl Colour $\Rightarrow$ By annotation \ldots} dialog to shade
the sequences by the long and short disorder predictors. {\sl Note how well the disordered regions predicted by each method agree
with the structure.}}}

\chapter{DNA and RNA Sequences}
\label{dnarna}
\section{Working with DNA}
\label{workingwithnuc}
Jalview was originally developed for the analysis of protein sequences, but
now includes some specific features for working with nucleic acid sequences
and alignments. Jalview recognises nucleotide sequences and alignments based on
the presence of nucleotide symbols [ACGT] in greater than 85\% of the
sequences. Built in codon-translation tables can be used to translate ORFs
into peptides for further analysis. ENA nucleotide records retrieved {\sl via} the
sequence fetcher (see Section \ref{fetchseq}) are also parsed in order to
identify codon regions and extract peptide products. Furthermore, Jalview
records mappings between protein sequences that are derived from regions of a
nucleotide sequence. Mappings are used to transfer annotation between
nucleic acid and protein sequences, and to dynamically highlight regions in
one sequence that correspond to the position of the mouse pointer in another.
%TODO Working with Nucleic acid sequences and structures.
\subsection{Alignment and Colouring}

Jalview provides a simple colourscheme for DNA bases, but does not apply any
specific conservation or substitution score model for the shading of
nucleotide alignments. However, pairwise alignments performed using the {\sl Calculate $\Rightarrow$ Pairwise Alignment
\ldots} option will utilise an identity score matrix to calculate alignment
score when aligning two nucleotide sequences.

\subsubsection{Aligning Nucleic Acid Sequences}

Jalview has limited knowledge of the capabilities of the programs that
are made available to it {\sl via} web services, so it is up to you, the user,
to decide which service to use when working with nucleic acid sequences. The
table shows which alignment programs are most appropriate
for nucleotide alignment. Generally, all will work, but some may be more suited
to your purposes than others. We also note that none of these include
support for taking RNA secondary structure prediction into account when aligning
sequences (but will be providing services for this in the future!) 
\begin{table}{}
\centering
\begin{tabular}{|l|c|l|}
\hline
Program& NA support& Notes\\
\hline
ClustalW& Yes&\begin{minipage}[f]{3in}
Default is to autodetect nucleotide
sequences. Editable parameters include nucleotide substitution matrices and
distance metrics.
\end{minipage}

\\
\hline

Muscle& Yes (treat U as T)&\begin{minipage}[f]{3in}
Default is to autodetect nucleotide
sequences. Editable parameters include nucleotide substitution matrices and
distance metrics.
\end{minipage}

\\
\hline

MAFFT& Yes&\begin{minipage}[f]{3in}
Will autodetect nucleotide sequences and use a hardwired substitution model
(all amino-acid sequence related parameters are ignored). Unknown whether
substitution model treats Uracil specially.
\end{minipage}

\\
\hline

ProbCons& No&\begin{minipage}[f]{3in}
ProbCons has no special support for aligning nucleotide sequences. Whilst an
alignment will be returned, it is unlikely to be reliable.
\end{minipage}

\\
\hline

T-COFFEE& Yes&\begin{minipage}[f]{3in}
Sequence type is automatically detected and an appropriate
parameter set used as required. A range of nucleotide specific
score models are available.\end{minipage}

\\\hline
\end{tabular}
\caption{{\bf JABAWS Alignment programs suitable for aligning nucleic acid
sequences.} All JABAWS alignment services will return an alignment if provided
with RNA or DNA sequences, with varying reliability.}
\label{nucleomsatools}
\end{table}

\subsection{Translate cDNA}

The {\sl Calculate $\Rightarrow$ Translate cDNA} function in the alignment
window is only available when working with a nucleic acid alignment. It uses the standard codon translation table given in the online help documentation to translate a nucleotide alignment, or the currently selected region, into a set of aligned peptide sequences. Any features or annotation present on the nucleotide alignment will also be translated, allowing DNA alignment analysis results to be transferred on to peptide products for further investigation.

\subsection{Linked DNA and Protein Views}

\parbox{3.5in}{
Views of alignments involving DNA sequences are linked to views of alignments containing their peptide products in a similar way to views of protein sequences and views of their associated structures. Peptides translated from cDNA that have been fetched from ENA records for DNA contigs are linked to their `parent' coding regions. Mousing over a region of the peptide highlights codons in views showing the original coding region.
}\parbox{3in}{
\begin{center}
%\begin{figure}[htbp]

\includegraphics[width=2.8in]{images/cdnatranslinkedwin.pdf}

%\caption{{\bf Linked DNA and Protein Views.} }
%\end{figure}
\end{center}
}


\subsection{Coding Regions from ENA Records}

Many ENA records that can be retrieved with the sequence fetcher contain exons.
Coding regions will be marked as features on the ENA nucleotide sequence, and
Uniprot database cross references will be listed in the tooltip displayed when
the mouse hovers over the sequence ID. Uniprot database cross references
extracted from ENA records are sequence cross references, and associate a
Uniprot sequence's coordinate system with the coding regions annotated on the
ENA sequence. Jalview utilises cross-reference information in two ways.
\subsubsection{Retrieval of Protein or DNA Cross References}
The {\sl Calculate $\Rightarrow$ Get Cross References } function is only available when Jalview recognises that there are protein/DNA cross-references present on sequences in the alignment. When selected, it retrieves the cross references from the alignment's dataset (a set of sequence and annotation metadata shared between alignments) or using the sequence database fetcher. This function can be used for ENA sequences containing coding regions to open the Uniprot protein products in a new alignment window. The new alignment window that is opened to show the protein products will also allow dynamic highlighting of codon positions in the ENA record for each residue in the protein product(s).

\subsubsection{Retrieval of Protein Features on Coding Regions}

The Uniprot cross-references derived from ENA records can be used by Jalview to visualize protein sequence features directly on nucleotide alignments.
This is because the database cross references include the sequence coordinate mapping information to correspond regions on the protein sequence with that of the nucleotide contig. 
Jalview will use the Uniprot accession numbers associated with the sequence to retrieve features, and then map them onto the nucleotide sequence's coordinate system using 
the coding region location.

\begin{figure}[htbp]
\begin{center}
\label{dnadasfeatures}
\includegraphics[width=5in]{images/dnadasfeatures.pdf}

\caption{Uniprot and PDB sum features retrieved and mapped onto
coding regions of ENA record V00488 (an earlier version of Jalview is shown
here).}

\end{center}
\end{figure}

\exercise{Visualizing Protein Features on Coding Regions}
{
\exstep{Use the sequence fetcher to retrieve ENA record D49489.}
\exstep{Ensure that {\sl View $\Rightarrow$ Show Sequence Features} is checked and change the 
alignment view format to {\sl Wrapped} mode so the distinct exons can be seen.}
\exstep{Open the {\sl DAS Settings} tab in the {\sl Sequence Feature Settings\ldots} 
window {\sl View $\Rightarrow$ Features setting}
and fetch features for D49489 from the Uniprot reference server,
and any additional servers that work with the Uniprot coordinate system.}
\exstep{Mouse over the features retrieved, note that they have been mapped onto the coding regions, and in some cases broken into several parts to cover the distinct exons.}
\exstep{Open a new alignment view containing the Uniprot protein product 
with {\sl Calculate $\Rightarrow$ Get Cross References $\Rightarrow$ Uniprot } 
and examine the database references and sequence features. Experiment with the 
interactive highlighting of codon position for each residue.}
}
% \section{Working with RNA}
% \label{workingwithrna}
% 
% \subsection{RNA specific alignment colourschemes}
% \label{rnacolschemes}
% 
% \subsection{Exploring RNA secondary structure with VARNA}
% \label{varna}
% 
% \subsection{RNA Secondary structure annotation}
% \subsubsection{Interactive creation of RNA secondary structure annotation}
% \label{rnasecstrediting}
% 
% \subsubsection{Import and export of RNA secondary structure annotation}
% \label{rnasecstrio}


% \chapter{Advanced Jalview}
% 
% \section{Customising Jalview}
% \subsection{Setting preferences}
% 
% The Jalview Desktop stores configuration and history information in a file stored in the users home directory, called `.jalview\_properties'. Many of the options stored in this file are presented in the {\sl Desktop $\Rightarrow$ Tools $\Rightarrow$ Preferences\ldots} dialog. These preferences include default settings for : {\bf Visual} layout settings for alignment views and controlling the display of the default alignment, {\bf Connection} preferences such as the standard set of URL paths that are available from the links menu and the URL which is opened when a Sequence's ID is double clicked, {\bf Editing} settings like {\sl Pad Gaps} and autocalculation of consensus, {\bf Output} settings control the degree of meta-information written in alignment files and mode of EPS Figuregeneration, and finally the {\bf Das Settings} which allows the default DAS sources to be configured. 
% 
% \subsection{Adding your own URL links}
% 
% \subsection{Working with Databases and Database Cross References}
% \label{getcrossrefs}
% 
% {\sl Calculations $\Rightarrow$ Get Cross References }
% 
% \section{Jalview IO Interface}
% \subsection{Multiple views}
% \subsection{Annotation files}
% \subsection{Feature files}
% \subsection{Moving sequence associated annotation}
% \subsection{Propagating features}
% \section{Structures}
% \subsection{Working with Modeller files}
% \subsection{Using local PDB files}
% \section{Pairwise alignments}

\section{Working with RNA}
Jalview allows the creation of RNA secondary structure annotation, and includes
the VARNA secondary structure viewer for the display of RNA base pair diagrams.
It also allows the extraction of RNA secondary structure from 3D data when
available.

\subsection{Performing RNA Secondary Structure Predictions}
Secondary structure consensus calculations can be performed by enabling the
VIENNA service {\sl via} the {\sl Web Service $\Rightarrow$ Secondary
Structure} menu. These consensus structures are created by analysing the
covariation patterns in all visible sequences on the alignment. For more
information see the VIENNA documentation.

\begin{figure}[htbp]
\begin{center}
\label{rnaviennaservice}
\includegraphics[width=5in]{images/rnaViennaServiceWindow.pdf}

\caption{Secondary structure consensus calculations can be performed by enabling the
VIENNA service {\sl via} the {\sl Web Service $\Rightarrow$ Secondary
Structure} menu.}

\end{center}
\end{figure}

\begin{figure}[htbp]
\begin{center}
\label{rnaviennaaltpairs}
\includegraphics[width=5in]{images/rnaViennaAlternateProbs.pdf}

\caption{VIENNA can calculate alternate RNA base pairing probabilities. These
are shown in Jalview as tool-tips on the RNA secondary structure probability
score.}

\end{center}
\end{figure}


\exercise{Viewing RNA Structures}
{ \label{viewingrnaex}

\exstep{Import RF00162 from the Rfam (Seed) source using {\sl Fetch sequence(s)}
from the Desktop's File menu.} 

\exstep{Select {\sl Colour by RNA Helices} to
shade the alignment by the secondary structure annotation provided by Rfam.}

\exstep{Open VARNA with {\sl Structure $\Rightarrow$ View Structure
$\Rightarrow$ RNA Secondary Structure}.
In the VARNA Structures Manager toggle between (i) secondary structure
(alignment) (with gaps) and (ii) trimmed secondary structure (alignment). 
Explore the difference between trimmed and untrimmed views.
Click on different residues in the VARNA diagram - you should also see them
highlighted and selected in the sequence alignment window.}

\exstep{In the VARNA Structures Manager, right click on display window to
bring up the pop up context menu. Explore the options within the File, Export,
Display and Edit sections.

{\em VARNA views are stored in Jalview project files, in the same way as 3D
structure views produced by Jmol and Chimera.}}

\exstep{Enable the calculation and display of an RNAAliFold secondary structure
prediction for the alignment by selecting {\sl Web Service $\Rightarrow$ Secondary
Structure Prediction $\Rightarrow$ RNAAliFold }.}
% Compare this with the annotationline provided by Rfam.

\exstep{Edit the RNAAliFold calculation settings to show
Base Pair probabilities. Explore how editing the alignment affects the consensus
calculation.}

\exstep{Import 2GIS from the PDB database into a new window with {\sl Fetch
sequence(s)}.}

\exstep{Click on a sequence in Sequence ID panel and select {\sl Structure
$\Rightarrow$ View Structure $\Rightarrow$ 2GIS}, to view the structure in Jmol
window. Click on different residues and located them in the sequence alignment window.}

%\exstep{Add and link a Jmol structure view
%for Bacillus\_amyloliquef.9 for 3NPB (from the PDB). Display the secondary
%structure along-side the consensus structure for the alignment by adding
%reference annotation from the 3D structure.

%{\sl Hint: You need to make sure the RNAview service is enabled in your {\sl
%Structure} preferences to obtain RNA secondary structure annotation from PDB
%files.}}

 }

\chapter{Webservices}
\label{jvwebservices}
The term ``Webservices'' refers to a variety of data exchange
mechanisms based on HTTP.\footnote{HTTP: Hyper-Text Transfer Protocol.} 

\parbox[c]{4.5in}{Jalview can exploit public webservices to access databases
remotely, and also submit data to public services by opening pages with your web browser. These types of
services are `one-way', {\sl i.e.} data is either sent to the webservice or
retrieved from it by Jalview. The desktop application can also interact
with `two-way' remote analysis services in order to offload computationally
intensive tasks to High Performance Computing facilities. Most of these two-way
services are provided by {\bf Ja}va {\bf B}ioinformatics {\bf A}nalysis {\bf
W}eb {\bf S}ervice (JABAWS) servers\footnote{See
http://www.compbio.dundee.ac.uk/jabaws for more information and to download
your own server.}, which provides an easily installable system for performing
a range of bioinformatics analysis tasks. }
\parbox[c]{1.75in}{\includegraphics[width=1.65in]{images/wsmenu.pdf}}

\subsection{One-Way Web Services}

There are two types of one way service in Jalview. Database services,
which were introduced in in Section \ref{fetchseq}, provide sequence and
alignment data. They can also be used to add sequence IDs to an alignment
imported from a local file, prior to further annotation retrieval, as described
in Section \ref{featuresfromdb}.
% The final type of one way service are sequence
% and ID submission services.
% exemplified by the `Envision2 Services' provided
% by the ENFIN Consortium\footnote{ENFIN is the European Network for Functional
% INtegration. Please see http://www.enfin.org for more information. }.

% \subsubsection{One-way submission services}
% Jalview can use the system's web browser to submit sets of sequences and
% sequence IDs to web based applications. Single sequence IDs can be passed to
% a web site using the user definable URL links listed under the {\sl
% Links} submenu of the sequence ID popup menu. These are configured
% in the {\sl Connections} tab of the {\sl Preferences} dialog box.
% 
% The Envision 2 services presented in the webservice menu provides are the first
% example of one-way services where multiple sequences or sequence IDs can be
% sent. The {\sl Web service $\Rightarrow$ Envision 2 Services} menu entry
% provides two sub-menus that enable you to submit the sequences or IDs
% associated with the alignment or just the currently selected sequences to one
% of the Envision2 workflows. Selecting any one will open a new browser window on
% the Envision2 web application. The menu entries and their tooltips provide
% details of the Envision2 workflow and the dataset set that will be submitted
% ({\sl i.e.} the database reference type, or associated sequence subset). Please
% note, due to technical limitations, Jalview can currently only submit small
% numbers of sequences to the workflows - if no sequence or ID submissions are
% presented in the submenus, then try to select a smaller number of sequences to
% submit. 

\subsection{Remote Analysis Web Services}
Remote analysis services enable Jalview to use external computational
facilities. There are currently three types of service - multiple sequence
alignment, protein secondary structure prediction, and alignment analysis.
Many of these are provided by JABA servers, which are described at the end of
this section. In all cases, Jalview will construct a job based on the alignment
or currently selected sequences, ask the remote server to run the job, monitor
status of the job and, finally, retrieve the results of the job and display
them. The Jalview user is kept informed of the progress of the job through a
status window.

Currently, web service jobs and their status windows are not stored in Jalview
Project Files\footnote{This may be rectified in future versions.}, so it is
important that you do not close Jalview whilst a job is running. It is also
essential that you have a continuous network connection in order to
successfully use web services from Jalview, since it periodically checks the
progress of running jobs.


\subsection{JABA Web Services for Sequence Alignment and Analysis}
\label{jabaservices}
JABA stands for ``JAva Bioinformatics Analysis'', which is a system developed
by Peter Troshin and Geoff Barton at the University of Dundee for running
computationally intensive bioinformatics analysis programs. A JABA installation
typically provides a range of JABA web services (JABAWS) for use by other
programs, such as Jalview.

Exercises in the remainder of this section will demonstrate the simplest way of
installing JABA on your computer, and configuring Jalview so it can access the JABA services. If you
need any further help or more information about the services, please go to the
\href{http://www.compbio.dundee.ac.uk/jabaws}{JABAWS home page}.
%% \subsubsection{Aims}
%%  \begin{list}{$\bullet$}{}
%%  \item Gain experience using the different alignment services provided by
% JABA
%%\item Learn about the way that Jalview stores user presets for JABA services
%%\item Learn how to install JABA services and configure Jalview to access them
%%\end{list}

\subsection{Changing the Web Services Menu Layout}
\label{changewsmenulayout}
If you are working with a lot of different JABA services, you may wish to change
the way Jalview lays out the web services menu. You can do this from the Web
Services tab of the {\sl Preferences} dialog box.

\exercise{Changing the Layout of the Web Services Menu}{
\label{changewsmenulayoutex}
\exstep{Make sure you have loaded an alignment into Jalview, and examine the
current layout of the alignment window's {\sl Web Service} menu.}
\exstep{Open the preferences dialog box and select the web services tab.}
\exstep{Ensure the {\sl Enable JABAWS services} checkbox is selected, and unselect
the {\sl Enable Enfin Services} checkboxes.}
\exstep{Hit {\sl Refresh Services} to update the web services menu -- once the
progress bar has completed, open the {\sl Web Service} menu to view the changes.}
\exstep{Select the {\sl Index by host} checkbox and refresh the services once again.

{\sl Observe the way the layout of the JABAWS Alignment submenu changes.}
}
\exstep{Do the same with the {\sl Index by type} checkbox.} 
}

Jalview provides these options for configuring the layout of the  {\sl Web Service}
menu because different Jalview users may have access to a different number of
JABA services, and each will have their own preference regarding the layout of
the menu.

\begin{figure}[htbc]
\begin{center}
\includegraphics[width=3in]{images/jvjabawsconfig.pdf}
\caption{{\bf The Jalview Web Services preferences panel.} Options are provided
for configuring the list of JABA servers that Jalview will use, enabling and
disabling Enfin services, and configuring the layout of the web services
menu.}
\label{jvjabawsconfig}
\end{center}
\end{figure}


\subsubsection{Testing JABA services}
The JABAWS configuration dialog shown in Figure \ref{jvjabawsconfig} has colour
codes to indicate whether the Desktop can access the server, and whether all
services advertised by the server are functional. The colour codes are:

\begin{list}{$\bullet$}{}
  \item Red - Server cannot be contacted or reports a connection error.
  \item Amber - Jalview can connect, but one or more services are non-functional.
  \item Green - Server is functioning normally.
\end{list}
  %TODO green and a tick, red and a cros, amber and a value indicating whether its all going

Test results from JABAWS are reported on Jalview's console output (opened from
the Tools menu). Tests are re-run every time Jalview starts, and when the
[Refresh Services] button is pressed on the Jalview JABAWS configuration panel.

\subsubsection{Resetting the JABA Services Setting to their Defaults}
Once you have configured a JABAWS server and selected the OK button of the
preferences menu, the settings will be stored in your Jalview preferences file,
along with any preferences regarding the layout of the web services menu. If
you should ever need to reset the JABAWS server list to its defaults, use the
`Reset Services' button on the Web Services preferences panel.

\subsection{Running your own JABA Server}
You can download and run JABA on your own machine using the `VMWare' or
VirtualBox virtual machine environments. If you would like to do
this, there are full instructions at the
\href{http://www.compbio.dundee.ac.uk/jabaws/}{JABA web site}.

\exercise{Installing a JABA Virtual Machine on your Computer}{
\label{jabawsvmex}{\sl This tutorial will demonstrate the simplest way of
installing JABA on your computer, and configuring Jalview so it can access the JABA services. 

{\bf Prerequisites}

You will need a copy of VMWare Player/Workstation/Fusion on your machine.
}

\exstep{If you do not have VMWare player installed, download it from
www.vmware.com (this takes a few minutes -- you will need to register and wait
for an email with a download link).}
\exstep{Download the JABA virtual appliance archive called `jaba-vm.zip' from
\textsf{http://www.compbio.dundee.ac.uk/jabaws/archive/jabaws-vm.zip}

WARNING: This is large (about 300MB) and will take some time to download.
}
\exstep{Unpack the archive's contents to a place on your machine with at least
2GB of free space (On Windows, right click on the archive, and use the 'Extract
archive..' option).
}
\exstep{Open the newly extracted directory and double click the VMWare virtual
machine configuration file (jabaws.vcf). This will launch the VMWare player.
}
\exstep{Once VMWare player has started up, it may ask the question ``Did you move or copy
this virtual appliance?'' -- select `Copy'.}
\exstep{You may be prompted to download the VMWare linux tools. These are not
necessary, so close the window or click on `Later'.}
\exstep{You may also be prompted to install support for one or more devices (USB
or otherwise). Say `No' to these options.}
\exstep{Once the machine has loaded, it will display a series of IP addresses
for the different services provided by the VM. Make a note of the JABAWS URL --
this will begin with `http:' and end with `/jabaws''.}
}

\exercise{Configuring Jalview to Access your new JABAWS Virtual Appliance}{
\label{confnewjabawsappl}
\exstep{Start Jalview (If you have not done so already).} 
\exstep{Enable the Jalview Java Console by selecting its option from the Tools
menu.

{\sl Alternately, use the System Java console if you have
configured it to open when Jalview is launched, {\sl via} your system's Java
preferences (under the `Advanced' tab on Windows).}}
\exstep{Open the {\sl Preferences} dialog and locate the Web Services tab.}
\exstep{Add the URL for the new JABAWS server you started in Exercise
\ref{jabawsvmex} to the list of JABAWS urls using the `New Service
URL' button.}
\exstep{You will be asked if you want to test the service. Hit `Yes' to do this
-- you should then see some output in the console window.

{\sl Take a close look at the output in the console.  What do you think is
happening?}
}
\exstep{Hit OK to save your preferences -- you have now added a new JABA
service to Jalview!}
\exstep{Try out your new JABA services by loading the ferredoxin sequences from
http://www.jalview.org/tutorial/alignment.fa}
\exstep{Launch an alignment using one
of the JABA methods provided by your server. It will be listed under the JABAWS Alignment submenu of the {\sl Web Service} menu on the alignment window.

{\sl Note: You can watch the JABA VM appliance's process working by opening the
process monitor on your system. (On Windows XP, this involves right-clicking the
system clock and opening the task manager -- then selecting the 'Processes' tab
and sort by CPU).}
}
}

\end{document}