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@@ -1,7 +1,7 @@
+
+ Alignment Window Menus
+
+
+ - File
+
+ - Fetch Sequence
Shows
+ a dialog window in which you can retrieve known ids from
+ UniProt, EMBL, EMBLCDS, PFAM, Rfam, or PDB database using
+ Web Services provided by the European Bioinformatics
+ Institute. See Sequence
+ Fetcher
+ .
+ - Add Sequences
Add
+ sequences to the visible alignment from file, URL, or cut
+ & paste window
+ - Reload
Reloads the
+ alignment from the original file, if available.
Warning:
+ This will delete any edits, analyses and colourings
+ applied since the alignment was last saved, and cannot be
+ undone.
+ - Save (Control S)
+ Saves the alignment to the file it was loaded from (if
+ available), in the same format, updating the original in
+ place.
+ - Save As (Control Shift S)
+ Save the alignment to local file. A file selection
+ window will open, use the "Files of type:"
+ selection box to determine which alignment
+ format to save as.
+
+ - Output to Textbox
+ The alignment will be displayed in plain text in a new
+ window, which you can "Copy and Paste" using the
+ pull down menu, or your standard operating system copy and
+ paste keys. The output window also has a "New
+ Window" button to import the (possibly edited) text
+ as a new alignment.
Select the format of the text
+ by selecting one of the following menu items.
+
+
+ - FASTA
+ - MSF
+ - CLUSTAL
+ - BLC
+ - PIR
+ - PFAM
+ - PileUp
+ - AMSA
+ - STH
+ - Phylip
+ - JSON
+
+ - Page Setup ...
Open
+ the printing system's Page Setup dialog box, to control page
+ size, layout and orientation.
+ - Print (Control P)
+ Jalview will print the alignment using the current
+ fonts and colours of your alignment. If the alignment has
+ annotations visible, these will be printed below the
+ alignment. If the alignment is wrapped the number of
+ residues per line of your alignment will depend on the paper
+ width or your alignment window width, whichever is the
+ smaller.
+ - Export Image
+ Creates an alignment graphic with the current view's
+ annotation, alignment background colours and group colours.
+ If the alignment is wrapped,
+ the output will also be wrapped and will have the same
+ visible residue width as the open alignment.
+
+ - Export Features
All
+ features visible on the alignment can be saved to file or
+ displayed in a textbox in either Jalview or GFF format
+ - Export Annotations
+ All annotations visible on the alignment can be saved to
+ file or displayed in a textbox in Jalview annotations
+ format.
+ - Load Associated Tree
+ Jalview can view
+ trees stored in the Newick file format, and associate them
+ with the alignment. Note: the ids of the tree file and your
+ alignment MUST be the same.
+
+ - Load Features / Annotations
+ Load files describing precalculated sequence
+ features or alignment
+ annotations.
+
+ - Close (Control W)
Close
+ the alignment window. Make sure you have saved your
+ alignment before you close - either from the Desktop's Save
+ Project File menu option, or by using the Save
+ As menu.
+
+
+ - Edit
+
+ - Undo (Control Z)
+ This will undo any edits you make to the alignment. This
+ applies to insertion or deletion of gaps, cutting residues
+ or sequences from the alignment or pasting sequences to the
+ current alignment or sorting the alignment. NOTE:
+ It DOES NOT undo colour changes, adjustments to group sizes,
+ or changes to the annotation panel.
+ - Redo (Control Y)
+ Any actions which you undo can be redone using redo.
+ - Cut (Control X)
+ This will make a copy of the currently selected
+ residues before removing them from your alignment. Click on
+ a sequence name if you wish to select a whole sequence.
+ Use <CTRL> and X (<APPLE> and X on MacOSX) to
+ cut.
+
+ - Copy (Control C)
Copies
+ the currently selected residues to the system clipboard -
+ you can also do this by pressing <CTRL> and C
+ (<APPLE> and C on MacOSX).
If you try to
+ paste the clipboard contents to a text editor, you will see
+ the format of the copied residues FASTA.
+
+ - Paste
+
+ - To New Alignment (Control Shift V)
+ A new alignment window will be created from
+ sequences previously copied or cut to the system
+ clipboard.
Use <CTRL> and <SHIFT>
+ and V(<APPLE> and <SHIFT;> and and V on
+ MacOSX) to paste.
+
+ - Add To This Alignment (Control V)
+ Copied sequences from another alignment window can
+ be added to the current Jalview alignment.
+
+ - Delete (Backspace)
+ This will delete the currently selected residues
+ without copying them to the clipboard. Like the other edit
+ operations, this can be undone with Undo.
+
+ - Remove Left (Control L)
+ If the alignment has marked columns, the alignment will
+ be trimmed to the left of the leftmost marked column. To
+ mark a column, mouse click the scale bar above the
+ alignment. Click again to unmark a column, or select
+ "Deselect All" to deselect all columns.
+ - Remove Right (Control R)
+ If the alignment has marked columns, the alignment will
+ be trimmed to the right of the rightmost marked column. To
+ mark a column, mouse click the scale bar above the
+ alignment. Click again to unmark a column, or select
+ "Deselect All" to deselect all columns.
+ - Remove Empty Columns (Control E)
+ All columns which only contain gap characters
+ ("-", ".") will be deleted.
You
+ may set the default gap character in preferences.
+
+ - Remove All Gaps (Control Shift E)
+ Gap characters ("-", ".") will be
+ deleted from the selected area of the alignment. If no
+ selection is made, ALL the gaps in the alignment will be
+ removed.
You may set the default gap character in preferences.
+
+ - Remove Redundancy (Control D)
+ Selecting this option brings up a window asking you to
+ select a threshold. If the percentage identity between any
+ two sequences (under the current alignment) exceeds this
+ value then one of the sequences (the shorter) is discarded.
+ Press the "Apply" button to remove redundant
+ sequences. The "Undo" button will undo the last
+ redundancy deletion.
+ - Pad Gaps
+ When selected, the alignment will be kept at minimal
+ width (so there are no empty columns before or after the
+ first or last aligned residue) and all sequences will be
+ padded with gap characters before and after their
+ terminating residues.
This switch is useful when
+ making a tree using unaligned sequences and when working
+ with alignment analysis programs which require 'properly
+ aligned sequences' to be all the same length.
You
+ may set the default for Pad Gaps in the preferences.
+
+
+ - Select
+
+ - Find...
+ (Control F)
Opens the Find dialog box to
+ search for residues, sequence name or residue position
+ within the alignment and create new sequence features from
+ the queries.
+ - Select All (Control A)
+ Selects all the sequences and residues in the
+ alignment.
Use <CTRL> and A (<APPLE>
+ and A on a MacOSX) to select all.
+
+ - Deselect All (Escape)
+ Removes the current selection box (red dashed box) from
+ the alignment window. All selected sequences, residues and
+ marked columns will be deselected.
Use
+ <ESCAPE> to deselect all.
+
+ - Invert Sequence Selection (Control I)
+ Any sequence ids currently not selected will replace
+ the current selection.
+ - Invert Column Selection (Control Alt
+ I)
+ Any columns currently not selected will replace the
+ current column selection.
+ - Create Group (Control G)
Create
+ a group containing the currently selected sequences.
+ - Remove Group (Shift Control G)
+ Ungroup the currently selected sequence group.
+ - Make Groups for selection
The
+ currently selected groups of the alignment will be
+ subdivided according to the contents of the currently
+ selected region.
Use this to subdivide an alignment
+ based on the different combinations of residues at marked
+ columns.
+
+ - Undefine Groups (Control U)
+ The alignment will be reset with no defined groups.
+ WARNING: This cannot be undone.
+
+ - Select/Hide
+ Columns by Annotation
Select or Hide
+ columns in the alignment according to secondary structure,
+ labels and values shown in alignment annotation rows.
+ - Select Highlighted Columns
Selects
+ the columns currently highlighted as a result of a find, mouse
+ over, or selection event from a linked structure viewer or other
+ application. Modifiers will work on some platforms: ALT will add
+ all but the highlighted set to the column selection, and CTRL
+ (or META) will toggle the selection.
+
+ - View
+
+ - New View (Control T)
+ Creates a new view from the current alignment view.
+ - Expand Views (X)
+ Display each view associated with the alignment in its own
+ alignment window, allowing several views to be displayed
+ simultaneously.
+ - Gather Views (G)
+ Each view associated with the alignment will be displayed
+ within its own tab on the current alignment window.
+ - Show→(all Columns / Sequences /
+ Sequences and Columns)
All hidden Columns
+ / Sequences / Sequences and Columns will be revealed.
+ - Hide→(all Columns / Sequences /
+ Selected Region / All but Selected Region )
+ Hides the all the currently selected Columns / Sequences /
+ Region or everything but the selected Region.
+ - Automatic Scrolling
+ When selected, the view will automatically scroll to
+ display the highlighted sequence position corresponding to
+ the position under the mouse pointer in a linked alignment
+ or structure view.
+ - Show Sequence Features
Show
+ or hide sequence features on this alignment.
+ - Sequence
+ Feature Settings...
Opens the
+ Sequence Feature Settings dialog box to control the colour
+ and display of sequence features on the alignment, and
+ configure and retrieve features from DAS annotation
+ servers.
+ - Sequence ID Tooltip
+ (application only)
This submenu's options allow the
+ inclusion or exclusion of non-positional sequence features
+ or database cross references from the tooltip shown when the
+ mouse hovers over the sequence ID panel.
+
+ - Alignment Properties...
+ Displays some simple statistics computed for the
+ current alignment view and any named properties defined on
+ the whole alignment.
+ - Overview
+ Window
A scaled version of the alignment
+ will be displayed in a small window. A red box will indicate
+ the currently visible area of the alignment. Move the
+ visible region using the mouse.
+
+ - Annotations (Since Jalview 2.8.2)
+
+ - Show Annotations
+ If this is selected the "Annotation Panel"
+ will be displayed below the alignment. The default setting
+ is to display the conservation calculation, quality
+ calculation and consensus values as bar charts.
+ - Show Alignment Related
+ Show all annotations that are for the alignment as a whole
+ (for example, Consensus, or secondary structure prediction
+ from alignment).
+ - Hide Alignment Related
+ Hide all annotations that are for the alignment as a whole.
+ - Show Sequence Related
+ Show all annotations that are for individual sequences.
+ - Hide Sequence Related
+ Hide all annotations that are for individual sequences.
+ - You can also selectively show or hide
+ annotations from the Popup or
+ Annotation menus.
+
+ - Sort by Sequence
Sort
+ sequence-specific annotations by sequence order in the
+ alignment (and within that, by label).
+ - Sort by Label
Sort
+ sequence-specific annotations by label (and within that, by
+ sequence order). If neither sort order is selected, no
+ sorting is applied, allowing you to make a manual ordering
+ of the annotations.
+ - Autocalculated Annotation
+ Settings for the display of autocalculated annotation.
+
+ - Show first
Show
+ autocalculated annotations above sequence-specific
+ annotations. Note this also applies to other annotations
+ for the alignment, for example secondary structure
+ prediction from alignment.
+ - Show last
Show
+ autocalculated / alignment annotations below
+ sequence-specific annotations.
+ - Apply to all groups
+ When ticked, any modification to the current
+ settings will be applied to all autocalculated
+ annotation.
+ - Show Consensus Histogram
+ Enable or disable the display of the histogram
+ above the consensus sequence.
+ - Show Consensus Logo
+ Enable or disable the display of the Consensus
+ Logo above the consensus sequence.
+ - Normalise Consensus Logo
+ When enabled, scales all logo stacks to the same
+ height, making it easier to compare symbol diversity in
+ highly variable regions.
+ - Group Conservation
+ When ticked, display a conservation row for all
+ groups (only available for protein alignments).
+ - Group Consensus
+ When ticked, display a consensus row for all
+ groups.
+
+
+ - Alignment Window Format Menu
+
+ - Font...
+ Opens the "Choose Font" dialog box, in order
+ to change the font of the display and enable or disable
+ 'smooth fonts' (anti-aliasing) for faster alignment
+ rendering.
+ - Wrap
+ When ticked, the alignment display is "wrapped" to
+ the width of the alignment window. This is useful if your
+ alignment has only a few sequences to view its full width at
+ once.
+
Additional options for display of sequence numbering
+ and scales are also visible in wrapped layout mode:
+
+ - Scale Above
+ Show the alignment column position scale.
+ - Scale Left
Show
+ the sequence position for the first aligned residue in
+ each row in the left column of the alignment.
+ - Scale Right
+ Show the sequence position for the last aligned residue
+ in each row in the right-most column of the alignment.
+ - Show Sequence Limits
+ If this box is selected the sequence name will have
+ the start and end position of the sequence appended to
+ the name, in the format NAME/START-END
+ - Right Align Sequence ID
+ If this box is selected then the sequence names
+ displayed in the sequence label area will be aligned
+ against the left-hand edge of the alignment display,
+ rather than the left-hand edge of the alignment window.
+
+ - Show Hidden Markers
+ When this box is selected, positions in the
+ alignment where rows and columns are hidden will be
+ marked by blue arrows.
+ - Boxes
If this is
+ selected the background of a residue will be coloured
+ using the selected background colour. Useful if used in
+ conjunction with "Colour Text."
+ - Text
+ If this is selected the residues will be displayed
+ using the standard 1 character amino acid alphabet.
+ - Colour Text
+ If this is selected the residues will be coloured
+ according to the background colour associated with that
+ residue. The colour is slightly darker than background
+ so the amino acid symbol remains visible.
+ - Show Gaps
+ When this is selected, gap characters will be
+ displayed as "." or "-". If
+ unselected, then gap characters will appear as blank
+ spaces.
You may set the default gap character
+ in preferences.
+
+ - Centre Annotation Labels
+ Select this to center labels along an annotation
+ row relative to their associated column (default is off,
+ i.e. left-justified).
+ - Show Unconserved
+ When this is selected, all consensus sequence
+ symbols will be rendered as a '.', highlighting
+ mutations in highly conserved alignments.
-
-
-
+
-
-
+
+
- Colour
-
- - Apply Colour To All Groups
If
- this is selected, any changes made to the background colour will
- be applied to all currently defined groups.
-
- - Colour
- Text...
Opens the Colour Text dialog box to
- set a different text colour for light and dark background, and the
- intensity threshold for transition between them.
-
- - Colour Scheme options: None, ClustalX,
- Blosum62 Score, Percentage Identity, Zappo, Taylor,
- Hydrophobicity, Helix Propensity, Strand Propensity, Turn
- Propensity, Buried Index, Nucleotide, Purine/Pyrimidine, User Defined
See
- colours for a
- description of all colour schemes.
- - By Conservation
See Colouring by
- Conservation.
- - Modify Conservation Threshold
Use
- this to display the conservation threshold slider window. Useful
- if the window has been closed, or if the 'by conservation' option
- appears to be doing nothing!
- - Above Identity Threshold
See
- Above Percentage
- Identity .
-
- - Modify Identity Threshold
Use
- this to set the threshold value for colouring above Identity.
- Useful if the window has been closed.
-
- - By Annotation
Colours
- the alignment on a per-column value from a specified annotation.
- See Annotation
- Colouring.
- - By RNA Helices
- Colours the helices of an RNA alignment loaded from a Stockholm file. See
- RNA Helices
- Colouring.
-
-
- Calculate
-
- - Sort
-
- - by ID
This will sort
- the sequences according to sequence name. If the sort is
- repeated, the order of the sorted sequences will be inverted.
-
- - by Length
This will
- sort the sequences according to their length (excluding gap
- characters). If the sort is repeated, the order of the sorted
- sequences will be inverted.
- - by Group
This
- will sort the sequences according to sequence name. If the sort
- is repeated, the order of the sorted sequences will be inverted.
-
- - by Pairwise Identity
This
- will sort the selected sequences by their percentage identity to
- the consensus sequence. The most similar sequence is put at the
- top.
- - The Sort
- menu will have some additional options if you have just done a
- multiple alignment calculation, or opened a tree viewer window.
-
-
-
- - Calculate Tree
Functions
- for calculating trees on the alignment or the currently selected
- region. See calculating
- trees.
-
- - Average Distance Using % Identity
- - Neighbour Joining Using % Identity
- - Average Distance Using Blosum62
- - Neighbour Joining Using Blosum62
-
-
- Note: Since Version 2.8.1, a number of additional similarity measures for tree calculation are provided in this menu.
-
- - Pairwise Alignments
Applies
- Smith and Waterman algorithm to selected sequences. See pairwise alignments.
-
- - Principal Component Analysis
Shows
- a spatial clustering of the sequences based on similarity scores calculated with
- the alignment. See Principal
- Component Analysis.
-
- - Extract Scores ... (optional)
This
- option is only visible if Jalview detects one or more white-space
- separated values in the description line of the alignment
- sequences.
When selected, these numbers are parsed into
- sequence associated annotation which can then be used to sort the
- alignment via the Sort by→Score menu.
-
- - Autocalculate Consensus
For
- large alignments it can be useful to deselect "Autocalculate
- Consensus" when editing. This prevents the sometimes lengthy
- calculations performed after each sequence edit.
-
- - Sort With New Tree
When
- enabled, Jalview will automatically sort the alignment when a new
- tree is calculated or loaded onto it.
- - Show Flanking Regions
Opens
- a new alignment window showing any additional sequence data either
- side of the current alignment. Useful in conjunction with 'Fetch
- Database References' when the 'Trim Retrieved Sequences' option is
- disabled to retrieve full length sequences for a set of aligned
- peptides.
-
-
- Web Service Menu
This menu
- is dynamic, and may contain user-defined web service entries in
- addition to any of the following ones:
-
- - Fetch DB References
This
- submenu contains options for accessing any of the database services
- that Jalview is aware of (e.g. DAS sequence servers and the
- WSDBFetch service provided by the EBI) to verify sequence start/end
- positions and retrieve all database cross references and PDB ids
- associated with all or just the selected sequences in the alignment.
+ - Colour
+
+ - Apply Colour To All Groups
+ If this is selected, any changes made to the background
+ colour will be applied to all currently defined groups.
+
+ - Colour
+ Text...
Opens the Colour Text dialog box
+ to set a different text colour for light and dark background,
+ and the intensity threshold for transition between them.
+ - Colour Scheme options: None, ClustalX,
+ Blosum62 Score, Percentage Identity, Zappo, Taylor,
+ Hydrophobicity, Helix Propensity, Strand Propensity, Turn
+ Propensity, Buried Index, Nucleotide, Purine/Pyrimidine, User
+ Defined
+ See colours
+ for a description of all colour schemes.
+
+ - By Conservation
+ See Colouring
+ by Conservation.
+
+ - Modify Conservation Threshold
+ Use this to display the conservation threshold slider
+ window. Useful if the window has been closed, or if the 'by
+ conservation' option appears to be doing nothing!
+ - Above Identity Threshold
+ See Above
+ Percentage Identity
+ .
+
+ - Modify Identity Threshold
+ Use this to set the threshold value for colouring above
+ Identity. Useful if the window has been closed.
+
+ - By Annotation
Colours
+ the alignment on a per-column value from a specified
+ annotation. See Annotation
+ Colouring.
+
+ - By RNA Helices
Colours
+ the helices of an RNA alignment loaded from a Stockholm file.
+ See RNA
+ Helices Colouring.
+
+
+ - Calculate
+
+ - Sort
- - 'Trim Retrieved Sequences' - when checked, Jalview will
- discard any additional sequence data for accessions associated with
- sequences in the alignment.
Note: Disabling this
- could cause out of memory errors when working with genomic
- sequence records !
Added in Jalview 2.8.1
-
- - 'Standard Databases' will check sequences against the EBI
- databases plus any active DAS sequence sources<
-
Other sub-menus allow you to pick a specific source to query -
- sources are listed alphabetically according to their nickname.
+ - by ID
This will
+ sort the sequences according to sequence name. If the sort
+ is repeated, the order of the sorted sequences will be
+ inverted.
+ - by Length
This
+ will sort the sequences according to their length
+ (excluding gap characters). If the sort is repeated, the
+ order of the sorted sequences will be inverted.
+ - by Group
This
+ will sort the sequences according to sequence name. If the
+ sort is repeated, the order of the sorted sequences will
+ be inverted.
+ - by Pairwise Identity
+ This will sort the selected sequences by their
+ percentage identity to the consensus sequence. The most
+ similar sequence is put at the top.
+ - The Sort
+ menu will have some additional options if you have just
+ done a multiple alignment calculation, or opened a tree
+ viewer window.
+
+
+ - Calculate Tree or PCA ...
Opens the
+ calculations dialog for
+ for calculating trees or
+ principle component analysis
+ plots on the alignment or the currently selected
+ region.
+
+ - Pairwise Alignments
Applies
+ Smith and Waterman algorithm to selected sequences. See pairwise
+ alignments.
-
- Selecting items from the following submenus will start a
- remote service on compute facilities at the University of Dundee, or
- elsewhere. You need a continuous network connection in order to use
- these services through Jalview.
-
-
- - Alignment
Align the currently
- selected sequences or all sequences in the alignment, or re-align
- unaligned sequences to the aligned sequences. Entries in this menu
- provide access to the various alignment programs supported by JABAWS. See the Multiple Sequence
- Alignment webservice client entry for more information.
- - Secondary Structure Prediction
-
- - JPred Secondary Structure Prediction
- Secondary structure prediction by network consensus. See
- the Jpred3 client entry for
- more information. The behaviour of this calculation depends on
- the current selection:
-
- - If nothing is selected, and the displayed sequences
- appear to be aligned, then a JNet prediction will be run for
- the first sequence in the alignment, using the current
- alignment. Otherwise the first sequence will be submitted for
- prediction.
- - If just one sequence (or a region on one sequence) has
- been selected, it will be submitted to the automatic JNet
- prediction server for homolog detection and prediction.
- - If a set of sequences are selected, and they appear to
- be aligned, then the alignment will be used for a Jnet
- prediction on the first sequence in the set
- (that is, the one that appears first in the alignment window).
-
-
-
- - Analysis
-
- - Multi-Harmony
Performs
- functional residue analysis on a protein family alignment with
- sub-families defined on it. See the Multi-Harmony service entry for more
- information.
-
-
-
-
+ Extract Scores ... (optional)
This
+ option is only visible if Jalview detects one or more
+ white-space separated values in the description line of the
+ alignment sequences.
When selected, these numbers are
+ parsed into sequence associated annotation which can then be
+ used to sort the alignment via the Sort by→Score menu.
+
+ Autocalculate Consensus
For
+ large alignments it can be useful to deselect
+ "Autocalculate Consensus" when editing. This
+ prevents the sometimes lengthy calculations performed after
+ each sequence edit.
+ Sort With New Tree
When
+ enabled, Jalview will automatically sort the alignment when a
+ new tree is calculated or loaded onto it.
+ Show Flanking Regions
Opens
+ a new alignment window showing any additional sequence data
+ either side of the current alignment. Useful in conjunction
+ with 'Fetch Database References' when the 'Trim Retrieved
+ Sequences' option is disabled to retrieve full length
+ sequences for a set of aligned peptides.
+
+
+ Web Service Menu
This menu
+ is dynamic, and may contain user-defined web service entries in
+ addition to any of the following ones:
+
+ - Fetch DB References
This
+ submenu contains options for accessing any of the database
+ services that Jalview is aware of (e.g. DAS sequence servers
+ and the WSDBFetch service provided by the EBI) to verify
+ sequence start/end positions and retrieve all database cross
+ references and PDB ids associated with all or just the
+ selected sequences in the alignment.
+
+ - 'Trim Retrieved Sequences' - when checked, Jalview
+ will discard any additional sequence data for accessions
+ associated with sequences in the alignment.
Note:
+ Disabling this could cause out of memory errors when
+ working with genomic sequence records !
Added
+ in Jalview 2.8.1
+
+ - 'Standard Databases' will check sequences against
+ the EBI databases plus any active DAS sequence sources
+
Other sub-menus allow you to pick a specific source to query
+ - sources are listed alphabetically according to their
+ nickname.
+
+
+ Selecting items from the following submenus will start a
+ remote service on compute facilities at the University of Dundee,
+ or elsewhere. You need a continuous network connection in order to
+ use these services through Jalview.
+
+ - Alignment
Align the
+ currently selected sequences or all sequences in the
+ alignment, or re-align unaligned sequences to the aligned
+ sequences. Entries in this menu provide access to the various
+ alignment programs supported by JABAWS. See the
+ Multiple Sequence
+ Alignment webservice client entry for more information.
+
+ - Secondary Structure Prediction
+
+ - JPred Secondary Structure Prediction
+ Secondary structure prediction by network
+ consensus. See the Jpred
+ client entry for more information. The behaviour of this
+ calculation depends on the current selection:
+
+ - If nothing is selected, and the displayed
+ sequences appear to be aligned, then a JPred prediction
+ will be run for the first sequence in the alignment,
+ using the current alignment. Otherwise the first
+ sequence will be submitted for prediction.
+ - If just one sequence (or a region on one
+ sequence) has been selected, it will be submitted to
+ the automatic JPred prediction server for homolog
+ detection and prediction.
+ - If a set of sequences are selected, and they
+ appear to be aligned, 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).
+
+
+
+
+ - Analysis
+
+ - Multi-Harmony
Performs
+ functional residue analysis on a protein family alignment
+ with sub-families defined on it. See the Multi-Harmony
+ service entry for more information.
+
+
+
+