a0dfc3a56c887efe60287e2f9ff43c9132592c98
dschmelt
  Tue Oct 13 11:56:59 2020 -0700
Creating announcements for refs #26321 and refs #25841

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 45795a1..fdb819b 100755
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -40,30 +40,54 @@
     <div class="col-sm-3">
       <ul>
         <li><a href="#2005">2005 News</a></li>
         <li><a href="#2004">2004 News</a></li>
         <li><a href="#2003">2003 News</a></li>
         <li><a href="#2002">2002 News</a></li>
         <li><a href="#2001">2001 News</a></li>
       </ul>
     </div>
   </div>
 </div>
 
 <!-- ============= 2020 archived news ============= -->
 <a name="2020"></a>
 
+<a name="101320"></a>
+<h2>Oct 13. 2020 &nbsp;&nbsp; Updated clinical tracks and features: LOVD, Decipher, and GeneReviews</h2>
+<p>
+We have updated three clinical tracks to add additional features.
+Decipher and LOVD Copy Number Variant (CNV) tracks now have the option to 
+&quot;Merge items that span the current region&quot;, collapsing items that
+are annotated across the entire Genome Browser visible region. Decipher now
+includes options to filter by Pathogenicity and Variant Class. GeneReviews now
+has a simple mouse-over which shows gene symbol and disease associations.<p>
+
+<ul>
+<li><a href="/cgi-bin/hgTrackUi?db=hg38&g=lovdComp">LOVD</a> 
+(<a href="/cgi-bin/hgTrackUi?db=hg38&g=lovdComp">hg38</a>/
+<a href="/cgi-bin/hgTrackUi?db=hg19&g=lovdComp">hg19</a>)</li>
+<li><a href="/cgi-bin/hgTrackUi?db=hg19&g=decipher">Decipher</a> 
+(<a href="/cgi-bin/hgTrackUi?db=hg19&g=decipher">hg19</a>)</li>
+<li><a href="/cgi-bin/hgTrackUi?db=hg38&g=geneReviews">GeneReviews</a> (<a href="/cgi-bin/hgTrackUi?db=hg38&g=geneReviews">hg38</a>/
+<a href="/cgi-bin/hgTrackUi?db=hg19&g=geneReviews">hg19</a>/<a href="/cgi-bin/hgTrackUi?db=hg18&g=geneReviews">hg18</a>)</li>
+</ul>
+<p>
+Thank you to the LOVD, Decipher, and GeneReviews teams for their curation of those 
+high-quality datasets. Thank you Genome Browser staff Kate Rosenbloom, Chris Lee, 
+and Daniel Schmelter for developing and releasing these feautre updates.</p>
+
 <a name="100520"></a>
 <h2>Oct. 5, 2020 &nbsp;&nbsp; New dbVar Common Structural Variants track</h2>
 <p>
 We are happy to release the dbVar composite tracks, providing a curated resource for structural 
 variant datasets on human GRCh37/hg19 and GRCh38/hg38 genome assemblies. 
 The track aggregates data from more than one hundred sources 
 including Gnomad, 1000 Genomes Consortium, and Decipher from the 
 <a href="https://www.ncbi.nlm.nih.gov/dbvar/content/overview/" 
 target="_blank">dbVar, the database of Structural Variation from NCBI</a>.
 The Common Structural Variants track shows variants that meet the following criteria:
 more than 50 basepairs, occur in at least 100 samples, and have an allele frequency of 
 &gt;=0.01 in at least one population. For more information, please see the
 track description page:</p>
 <ul>
 <li><a href="/cgi-bin/hgTrackUi?db=hg38&g=dbVarSv">dbVar Structural Variant track on hg38</a></li>