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+ * You should have received a copy of the GNU General Public License
+ * along with Jalview. If not, see .
+ * The Jalview Authors are detailed in the 'AUTHORS' file.
+ -->
Alignment Window Menus
-Alignment Window Menus
- File
-
- - Fetch Sequence
- Shows a dialog window in which you can select known ids from
- Uniprot, EMBL, EMBLCDS 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
-
-
- - 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 as a Jalview project 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 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 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 no empty columns before or after the first or last aligned
- residue) and all sequences will be padded with gap characters to the
- 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.
- - Undefine Groups (Control U)
- The alignment will be reset with no defined groups.
- WARNING: This cannot be undone.
- - Make Groups
- 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 observed at specific
- positions. (new in jalview 2.5)
-
-
- 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 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.
- - Autocalculated Annotation
Settings for the display of autocalculated annotation.
- -
- 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 Profile
- Enable or disable the display of the sequence logo above the consensus sequence.
-
- -
- Group Conservation
- When ticked, display a conservation row for all groups (only available for protein alignments).
-
- -
- Apply to all groups
- When ticked, display a consensus row for all groups.
-
-
-
- - Show Sequence Features
- Show or hide sequence features on this alignment.
- - Seqence
- 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.
-
-
- 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, 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.
-
-
-
- - 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
-
-
-
- - 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 the
- BLOSUM62 scores in 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.
-
-
-
- - Web Service
-
-
+ - 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.
+
+ 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.
+
+
+
+
+
-
- Selecting one of the following menu items starts a remote
- service on compute facilities at the University of Dundee. You need a
- continuous network connection in order to use these services through
- Jalview.
-
- - Alignment
-
- - ClustalW Multiple Sequence Alignment
- Submits all, or just the currently selected sequences for
- alignment with clustal W.
- - ClustalW Multiple Sequence Alignment
- Realign
- Submits the alignment or currently selected region for
- re-alignment with clustal W. Use this if you have added some new
- sequences to an existing alignment.
- - MAFFT Multiple Sequence Alignment
- Submits all, or just the currently selected region for
- alignment with MAFFT.
- - Muscle Multiple Protein Sequence Alignment
- Submits all, or just the currently selected sequences for
- alignment using Muscle. Do not use this if you are working with
- nucleic acid sequences.
-
-
- - Secondary Structure Prediction
-
- - JPred Secondary Structure Prediction
- Secondary structure prediction by network consensus. 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).
-
-
-
-
-
+
+ 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.
+
+
+ - Neighbour Joining Using PAM250
+ - Neighbour Joining Using Sequence
+ Feature Similarity
+ - Neighbour Joining Using Blosum62
+ - Neighbour Joining Using % Identity
+ - Average Distance Using PAM250
+ - Average Distance Using Sequence
+ Feature Similarity
+ - Average Distance Using Blosum62
+ - Average Distance Using % Identity
+
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.
+
+ - '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 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.
+
+
+
+
+