44a5e34356b1cff8c516354e2571223f9232296e
brianlee
  Tue Nov 23 12:52:04 2021 -0800
Adding news announcement for first GenArk hub blog post refs #27990

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       </ul>
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     <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>
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 <!-- ============= 2021 archived news ============= -->
+<a name="112321"></a>
+<h2>Nov. 23, 2021 &nbsp;&nbsp; First of three blog posts about new GenArk hubs</h2>
+<p>
+We are pleased to announce the first blog post in a three-part series about
+our new GenArk Assembly Hubs.
+This <a href="https://genome-blog.soe.ucsc.edu/blog/2021/11/23/genark-hubs-part-1/"
+target="_blank">first installment</a> explains what the GenArk hubs are, and
+shares a number of different ways to access their over 1500 genomes.</p>
+
 <a name="111821"></a>
 <h2>Nov. 18, 2021 &nbsp;&nbsp; New Clinical Rare Disease track - Orphadata</h2>
 <p>
 We are happy to share another clinical resource for genetic disease correlation, 
 <a href="/cgi-bin/hgTrackUi?db=hg38&g=orphadata">the Orphadata track</a> from 
 <a target="_blank" href="https://www.orpha.net/">the Orphanet consortium</a>. This 
 track shows nearly 8000 genes, on hg19 and hg38, 
 annotated with human disorders and epidemiological information 
 including Human Phenotype Ontology (HPO) disorder name, association type, 
 modes of inheritance, age of first symptoms, and disease prevalence (if available). 
 This data is gathered by a consortium of more than 40 countries, focusing 
 on rare diseases. This track includes gene-disease display filters
 based on association type, inheritance mode, and age of symptom onset.
 </p>
 <p>