6120d02a6aa7faf052299967d8bace2d2d706ad3 hiram Mon Dec 15 13:06:28 2025 -0800 one additional color code definition for paralogous annotations refs #35776 diff --git src/hg/makeDb/trackDb/TOGAv2.html src/hg/makeDb/trackDb/TOGAv2.html index 995cce59d39..40a83b03d08 100644 --- src/hg/makeDb/trackDb/TOGAv2.html +++ src/hg/makeDb/trackDb/TOGAv2.html @@ -78,30 +78,35 @@ <li><span style='display:inline-block; width:40px; height:15px; background-color:#828282;'> </span> <span style='color:#828282'>"missing"</span>: <50% of the CDS is present in the query and the middle 80% of the CDS exhibits no inactivating mutation. There is currently no evidence for transcript loss; however, the uncertainty is higher as more than half of the CDS is missing. Note that Missing transcripts can also arise if no genome alignment chain spans the transcript.</li> <li><span style='display:inline-block; width:40px; height:15px; background-color:#FFA078;'> </span> <span style='color:#FFA078'>"uncertain loss"</span>: there is at least one inactivating mutation in the middle 80% of the CDS, but evidence is not strong enough to classify the transcript as lost. These transcripts may or may not encode a functional protein.</li> <li><span style='display:inline-block; width:40px; height:15px; background-color:#FF3232;'> </span> <span style='color:#FF3232'>"lost"</span>: typically several inactivating mutations are present, thus there is strong evidence that the transcript is unlikely to encode a functional protein.</li> +<li><span style='display:inline-block; width:40px; height:15px; background-color:#9F8170;'> </span> + <span style='color:#9F8170'>"paralogous"</span>: Special category. Transcript is classified as paralogous +by TOGA2’s machine learning classifier and these are only retained if the respective query locus does not have +an orthologous projection. Transcripts in this color have enough inactivating mutations or missing sequence + such that there loss status is "missing" or "deleted".</li> </ul> </p> <p> Clicking on a transcript provides additional information about the orthology classification, inactivating mutations, the query's nucleotide/protein sequence, and protein/exon alignments. </p> <h2>Credits</h2> <p> This data was prepared by the <a href="https://www.senckenberg.de/en/research/institutes-overview/sf/ffm-dept-comparative-genomics/" target="_blank">Michael Hiller's Lab</a> </p> <h2>References</h2>