<html>
<!--
- * Jalview - A Sequence Alignment Editor and Viewer ($$Version-Rel$$)
- * Copyright (C) $$Year-Rel$$ The Jalview Authors
+ * Jalview - A Sequence Alignment Editor and Viewer (Version 2.9.0b1)
+ * Copyright (C) 2015 The Jalview Authors
*
* This file is part of Jalview.
*
</head>
<body>
- <p>
- <strong>Alignment Window Calculate Menu</strong>
- </p>
- <ul>
- <li><strong>Sort </strong>
- <ul>
- <li><strong>By ID</strong><em><br> This will sort the
- sequences according to sequence name. If the sort is repeated, the
- order of the sorted sequences will be inverted. </em>
- </li>
- <li><strong>By Length</strong><em><br> 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. </em>
- </li>
- <li><strong>By Group</strong><strong><br> </strong><em>This
- will sort the sequences according to sequence name. If the sort is
- repeated, the order of the sorted sequences will be inverted. </em><strong></strong>
- </li>
- <li><strong>By Pairwise Identity<br> </strong><em>This
- will sort the selected sequences by their percentage identity to
- the consensus sequence. The most similar sequence is put at the
- top. </em>
- </li>
- <li><em>The <a href="../calculations/sorting.html">Sort
- menu</a> will have some additional options if the alignment has any
- associated score annotation, or you have just done a multiple
- alignment calculation or opened a tree viewer window.</em><br></li>
- </ul></li>
+ <p>
+ <strong>Alignment Window Calculate Menu</strong>
+ </p>
+ <ul>
+ <li><strong>Sort </strong>
+ <ul>
+ <li><strong>By ID</strong><em><br> This will sort
+ the sequences according to sequence name. If the sort is
+ repeated, the order of the sorted sequences will be
+ inverted. </em></li>
+ <li><strong>By Length</strong><em><br> 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. </em></li>
+ <li><strong>By Group</strong><strong><br> </strong><em>This
+ will sort the sequences according to sequence name. If the
+ sort is repeated, the order of the sorted sequences will be
+ inverted. </em><strong></strong></li>
+ <li><strong>By Pairwise Identity<br>
+ </strong><em>This will sort the selected sequences by their
+ percentage identity to the consensus sequence. The most
+ similar sequence is put at the top. </em></li>
+ <li><em>The <a href="../calculations/sorting.html">Sort
+ menu</a> will have some additional options if the alignment
+ has any associated score annotation, or you have just done a
+ multiple alignment calculation or opened a tree viewer
+ window.
+ </em><br></li>
+ </ul></li>
<li><strong>Calculate Tree </strong> <br> <em>Functions
for calculating trees on the alignment or the currently selected
region. See <a href="../calculations/tree.html">calculating
<li><strong>Average Distance Using % Identity</strong></li>
</ul></li>
<li><strong>Pairwise Alignments</strong><br> <em>Applies
- Smith and Waterman algorithm to selected sequences. See <a
- href="../calculations/pairwise.html">pairwise alignments</a>.</em><br>
- </li>
- <li><strong>Principal Component Analysis</strong><br> <em>Shows
- a spatial clustering of the sequences based on similarity scores calculated over the alignment.. See <a href="../calculations/pca.html">Principal
- Component Analysis</a>.</em> <br></li>
- <li><strong>Extract Scores ... (optional)</strong><br> <em>This
- option is only visible if Jalview detects one or more white-space
- separated values in the description line of the alignment sequences.<br>
- 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.</em> <br></li>
- <li><strong>Translate as cDNA</strong> (not applet)<br><em>This option is visible for nucleotide alignments.
- Selecting this option shows the DNA's calculated protein product in a new <a href="../features/splitView.html">split frame</a> window. Note that the
- translation is not frame- or intron-aware; it simply translates all codons in each sequence, using the
- standard <a href="../misc/geneticCode.html">genetic code</a> (any incomplete final codon is discarded).
- You can perform this action on the whole alignment,
- or selected rows, columns, or regions.</em> <br></li>
- <li><strong>Get Cross-References</strong> (not applet)<br><em>This option is visible where sequences have cross-references to
- other standard databases; for example, an EMBL entry may have cross-references to one or more UNIPROT entries.
- Select the database to view all cross-referenced sequences in a new <a href="../features/splitView.html">split frame</a> window.</em> <br></li>
- <li><strong>Autocalculate Consensus</strong><br> <em>For
- large alignments it can be useful to deselect "Autocalculate
- Consensus" when editing. This prevents the sometimes lengthy
- calculations performed after each sequence edit.</em> <br></li>
- <li><strong>Sort Alignment With New Tree</strong><br> <em>If
- this option is selected, the alignment will be automatically sorted
- whenever a new tree is calculated or loaded.</em> <br>
- </li>
+ Smith and Waterman algorithm to selected sequences. See <a
+ href="../calculations/pairwise.html"
+ >pairwise alignments</a>.
+ </em><br></li>
+ <li><strong>Principal Component Analysis</strong><br> <em>Shows
+ a spatial clustering of the sequences based on similarity scores
+ calculated over the alignment.. See <a
+ href="../calculations/pca.html"
+ >Principal Component Analysis</a>.
+ </em> <br></li>
+ <li><strong>Extract Scores ... (optional)</strong><br> <em>This
+ option is only visible if Jalview detects one or more
+ white-space separated values in the description line of the
+ alignment sequences.<br> 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.
+ </em> <br></li>
+ <li><strong>Translate as cDNA</strong> (not applet)<br>
+ <em>This option is visible for nucleotide alignments. Selecting
+ this option shows the DNA's calculated protein product in a new
+ <a href="../features/splitView.html">split frame</a> window.
+ Note that the translation is not frame- or intron-aware; it
+ simply translates all codons in each sequence, using the
+ standard <a href="../misc/geneticCode.html">genetic code</a>
+ (any incomplete final codon is discarded). You can perform this
+ action on the whole alignment, or selected rows, columns, or
+ regions.
+ </em> <br></li>
+ <li><strong>Get Cross-References</strong> (not applet)<br>
+ <em>This option is visible where sequences have
+ cross-references to other standard databases; for example, an
+ EMBL entry may have cross-references to one or more UNIPROT
+ entries. Select the database to view all cross-referenced
+ sequences in a new <a href="../features/splitView.html">split
+ frame</a> window.
+ </em> <br></li>
+ <li><strong>Autocalculate Consensus</strong><br> <em>For
+ large alignments it can be useful to deselect
+ "Autocalculate Consensus" when editing. This prevents
+ the sometimes lengthy calculations performed after each sequence
+ edit.</em> <br></li>
+ <li><strong>Sort Alignment With New Tree</strong><br> <em>If
+ this option is selected, the alignment will be automatically
+ sorted whenever a new tree is calculated or loaded.</em> <br></li>
<li><strong>Show Flanking Regions</strong><br> <em>Opens
a new alignment window showing any additional sequence data
either side of the current alignment. Useful in conjunction with