10495f58d26155308dd4f24c7e3fed7e8202ea3e
ccpowell
  Thu Mar 21 15:23:16 2019 -0700
Adding new section to newarch.html for mastermind release, #21895

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 3927f0e..bff0248 100755
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -39,30 +39,58 @@
     </div>
     <div class="col-sm-3">
       <ul>
         <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>
 
 <!-- ============= 2019 archived news ============= -->
 <a name="2019"></a>
 
+<a name="032619"></a>
+<h2>
+Mar, 26 2019 &nbsp;&nbsp; New Genomenon Mastermind Variants track for Human (hg19)
+</h2>
+<p>
+We are pleased to announce the release of the Genomenon Mastermind Variants track for the 
+<a href="../cgi-bin/hgGateway?db=hg19" target="_blank">hg19/GRCh37 assembly</a>. This track is
+composed of variants found in scientific publications collected by <a 
+href="https://www.genomenon.com/" target="_blank">Genomenon Mastermind</a>. Mastermind uses
+software that searches for disease-gene-variant associations in the scientific literature. The
+genome browser track shows only if a variant has been indexed by the search engine. 
+Genomenon Mastermind Genomic Search Engine is a commercial database of variants likely to be 
+mentioned in full-text scientific articles.
+</p>
+<p>
+Genomic locations of variants are labeled with the nucleotide change. Hover over the features to
+see the gene, the amino acid change, and the scores MMCNT1, MMCNT2 and MMCNT3, described below. All
+other information is shown on the respective Mastermind variant detail page, accessible via the
+"Link to Mastermind" at the top of the details page.
+More information about this track and it's display can be found on the
+<a href="../cgi-bin/hgTrackUi?db=hg19&g=mastermind" target="_blank">track description</a> page.
+<p>
+We would like to give a big thank you to Mark Kiel, Steve Schwartz and Clayton Wheeler from
+Genomenon for making this data available as well as Max Haeussler, Conner Powell and the rest of the
+UCSC Genome Browser team for bringing this track to life.
+</p>
+
+
 <a name="030519"></a>
 <h2>
 Mar. 11, 2019 &nbsp;&nbsp; Addition of GRCh38 patch sequences to hg38
 </h2>
 <p>
 We are pleased to announce the addition of GRCh38 patches to the GRCh38/hg38 database. <a 
 href="https://www.ncbi.nlm.nih.gov/grc/human" target="_blank">Without a release date</a> for the 
 next coordinate-changing assembly, incorporating these sequences is an important step towards 
 providing the most up to date human assembly.</p>
 
 <p>
 This release includes new tracks visualizing patch sequences; the <a 
 href="../cgi-bin/hgTrackUi?db=hg38&g=fixSeqLiftOverPsl" target="_blank">Fix Patches</a> track
 represents error corrections, and the <a href="../cgi-bin/hgTrackUi?db=hg38&g=altSeqLiftOverPsl" 
 target="_blank">Alt Haplotypes</a> track represents novel patches (alt loci).</p>