f3ccc9b7200915518d9437f3718fd5b2097d9539 dschmelt Thu Jun 24 15:46:28 2021 -0700 Fixing inaccurate description refs #27142 diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html index 4e05071..ee63261 100755 --- src/hg/htdocs/goldenPath/newsarch.html +++ src/hg/htdocs/goldenPath/newsarch.html @@ -46,31 +46,32 @@ <li><a href="#2001">2001 News</a></li> </ul> </div> </div> </div> <!-- ============= 2021 archived news ============= --> <a name="2021"></a> <a name="062421"></a> <h2>June 24, 2021 New REVEL missense scores track for hg38 and hg19</h2> <p> The UCSC Genome Browser has just added the REVEL tracks to hg38 and hg19, a much requested clinical dataset, now visualized and interactive with our tools. REVEL scores predict the pathogenicity of missense variants for every possible -basepair change across the entire genome. This dataset bases its scores on 13 individual tools +basepair change across the entire genome's coding sequences. +This dataset bases its scores on 13 individual tools to produce high predictive performance of common and rare mutations. To learn more about the REVEL dataset, please visit their site below:</p> <ul> <li><a href="https://sites.google.com/site/revelgenomics/" target="_blank"> https://sites.google.com/site/revelgenomics</a></li> </ul> <p> To access these tracks on the Genome Browser, please visit their description pages below and change the tracks' visibility.</p> <ul> <li><a href="/cgi-bin/hgTrackUi?db=hg38&g=revel">REVEL track on hg38</a></li> <li><a href="/cgi-bin/hgTrackUi?db=hg19&g=revel">REVEL track on hg19</a></li> </ul> </p> <p>