<ul>\r
<li><strong>File</strong> \r
<ul>\r
+ <li><strong>Fetch Sequence</strong><br>\r
+ <em>Shows a dialog window in which you can select known ids from Uniprot, \r
+ EMBL, EMBLCDS or PDB database using Web Services provided by the European \r
+ Bioinformatics Institute. See <a href="features/seqfetch.html">Sequence \r
+ Fetcher</a></em>.</li>\r
<li><strong>Save As<br>\r
</strong><em>Save the alignment to local file. A file selection window \r
will open, use the "Files of type:" selection box to determine \r
<br>\r
Note: The retrieved information will update the sequence start and end \r
labels if they are incorrect. </em></li>\r
+ <li><strong>Seqence Settings </strong><br>\r
+ <em>If features have been added to the alignment then the priority of \r
+ rendering the features can be altered so that overlapping features can \r
+ be displayed or hidden. See <a href="features/seqfeatures.html">Sequence \r
+ Features</a>.</em></li>\r
<li><strong><a href="../features/overview.html">Overview Window</a><br>\r
</strong><em>A scaled version of the alignment will be displayed in a \r
small window. A red box will indicate the currently visible area of the \r
<li><strong>Principal Component Analysis</strong><br>\r
<em>Shows a spatial clustering of the sequences based on the BLOSUM62 \r
scores in the alignment. See <a href="../calculations/pca.html">Principal \r
- Component Analysis</a>.</em> <br>\r
+ Component Analysis</a>.</em> </li>\r
+ <li><strong>Translate cDNA</strong><br>\r
+ <em>If you are viewing a cDNA alignment a very simple translation service \r
+ is available. The translation ignores all gaps in the cDNA sequences. \r
+ </em> <br>\r
</li>\r
</ul>\r
</li>\r
sequences.</em></li>\r
</ul>\r
</li>\r
- <li><strong>Secondary Structure Prediction</strong>\r
+ <li><strong>Secondary Structure Prediction</strong> \r
<ul>\r
<li><strong>JPred Secondary Structure Prediction</strong><br>\r
<em>Secondary structure prediction by network consensus. The behaviour \r