5330311f9ba3e4a4ba14ff8e12748d7b2825b758
ccpowell
  Mon Jul 1 10:48:16 2019 -0700
Adding edits to dgvGold news release, #23371

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 395efc0..588e44a 100755
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -40,50 +40,50 @@
     <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="070119"></a>
-<h2>Jul. 1, 2019 &nsbp;nsbp New DGV Gold Standard track for human (GRCh19/hg19)</h2>
+<h2>Jul. 1, 2019 &nbsp;&nbsp New DGV Gold Standard track for human (GRCh19/hg19)</h2>
 <p>
 We are pleased to announce the DGV Gold Standard track for human (GRCh19/hg19). This track displays
 copy number variants (CNVs), insertions/deletions (InDels), inversions and inversion breakpoints
 annotated by the <a href="http://dgv.tcag.ca/dgv/app/home" target="_blank">Database of Genomic Variants</a>
-(DGV). The initial criteria for the Gold Standard set require that a variant is found in at least
+(DGV). The initial criteria for the Gold Standard set require that a variant be found in at least
 two different studies and found in at least two different samples. After filtering out low-quality
 variants, the remaining variants are clustered according to 50% minimum overlap, and then merged
 into a single record. Gains and losses are merged separately.
 </p>
 
 <p>
 The <a href="https://genome.ucsc.edu/cgi-bin/hgTrackUi?db=hg19&g=dgvPlus" target="_blank">DGV Gold Standard track</a>
 utilizes a boxplot-like display to represent the merging of records. The highest ranking variant in
 the cluster defines the inner &quot;box&quot;, while the outer lines define the outermost start and stop
 coordinates of the CNV. In this way, the inner box forms a high-confidence CNV location and the
-thin connecting lines indicate confidence intervals for the location of CNV.
+thin connecting lines indicate confidence intervals for the location of the CNV.
 </p>
 <p class="text-center">
-  <img class='text-center' src="../images/dgvGold-1.png" width='699' alt="DGV Gold Standard track">
+  <img class='text-center' src="../images/dgvGold.png" width='850' alt="DGV Gold Standard track">
 </p>
 
 <p>
 We would like to thank Jeff MacDonald and the <a href="http://dgv.tcag.ca/dgv/app/home" target="_blank">Database of Genomic Variants</a>
 group for providing guidance and these data. We would also like to thank Christopher Lee and Conner
 Powell as well as the entire UCSC Genome Browser team for creating and releasing this track.
 </p>
 
 <a name="062819"></a>
 <h2>Jun. 28, 2019 &nbsp;&nbsp; New Genome Browsers: Cow, bosTau9 (<em>Bos taurus</em>) and 
 Baboon, papAnu4 (<em>Papio anubis</em>)</h2>
 <p>
 Genome browsers are now available for the <em>Bos taurus</em> assembly released in Apr. 2018 by the
 <a href="https://www.ars.usda.gov/" target="_blank"> USDA Agricultural Research Service</a> (ARS-UCD1.2), 
 and the <em>Papio anubis</em> assembly released in Apr. 2017 by the