75d5363df141666b69816fac7d158bf97908cb6e lrnassar Mon Sep 28 16:53:30 2020 -0700 Adding date to title, no RM diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 7492c5b..7052edf 100755 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -85,31 +85,31 @@ <li>Filter on allele origin (somatic, germ line, de novo, etc.) now available on both tracks.</li> <li>Filter by molecular consequence (stop lost, nonsense, intron variant, etc.) now available on short variants track.</li> </ul> <p> Below is an example of the filter options available for the <b>ClinVar SNVs track</b>. For additional details on the updated display, see the <a target="_blank" href="/cgi-bin/hgTrackUi?db=hg38&c=chr1&g=clinvar">track description page</a>.</p> <p class="text-center"> <img class='text-center' src="../images/clinVarFilters.png" width='60%' alt="Example of filter options in ClinVar SNVs track"> </p> <a name="093020b"></a> -<h3>Changes to ClinGen and new tracks</h3> +<h3>Sept. 25, 2020   Changes to ClinGen and new tracks</h3> <p> We have created a new composite track, <a target="_blank" href="/cgi-bin/hgTrackUi?db=hg38&c=chr1&g=clinGenComp">ClinGen</a>, and deprecated the previous <a target="_blank" href="/cgi-bin/hgTrackUi?db=hg38&c=chr1&g=iscaComposite"> ClinGen CNVs track</a>. The ClinGen CNVs track will continue to be available, however, the data will no longer be updated. This was done by request of ClinGen, as all the data, as well as further updates, can be found in the <a target="_blank" href="/cgi-bin/hgTrackUi?db=hg38&g=clinvar">ClinVar Copy Number Variants (ClinVar CNVs) track</a>.</p> <p> The new <a target="_blank" href="/cgi-bin/hgTrackUi?db=hg38&g=clinGenComp">ClinGen composite track</a> includes three new tracks described below:</p> <ul> <li><b>ClinGen Dosage Sensitivity Map - Haploinsufficiency</b> - Shows evidence supporting or refuting haploinsufficiency (loss) as mechanisms for disease at gene-level and larger genomic regions.</li>