9c2dfa33b42a7ff3d3e21b70872d6fe3b7a62d0b
lrnassar
  Tue May 5 10:27:24 2020 -0700
Undoing and recomitting Ana's announcement - she accidentally changed the formatting on newsarchive page, no RM

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 53da55e..f7f768b 100755
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -44,58 +44,55 @@
         <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="050620"></a>
 <h2>May 6, 2020 &nbsp;&nbsp; Problematic Regions for NGS or Sanger sequencing or very variable regions</h2>
 <p>
 We are happy to announce a new data track which describes
-<a href="../../cgi-bin/hgTrackUi?db=hg19&g=problematic">Problematic Regions for NGS or Sanger sequencing or very variable regions</a> in the human assembly (hg19/GRCh37).
-</p>
+<a href="../../cgi-bin/hgTrackUi?db=hg19&g=problematic">Problematic Regions for NGS or Sanger sequencing or very variable regions</a> in the human assembly (hg19/GRCh37).</p>
 
 <p>
 This track shows genomic regions known to cause artefacts for common sequencing downstream analyses,
 like alignment, variant, or peak calling. This track is composed of 12 subtracks with underlying
-data imported from these projects:
-</p>
+data imported from these projects:</p>
 
 <ul>
 <li>
 <a href="../../cgi-bin/hgGateway">UCSC</a> - manually curated annotations of fixed sequences,
 alternate haplotypes, unplaced contigs, pseudo-autosomal regions, and mitochondria that can yield
 alignments with low quality mapping scores and discordant read pairs. </li>
 <li>
 <a href="https://personal.broadinstitute.org/anshul/projects/encode/rawdata/blacklists/hg19-
 blacklist-README.pdf">ENCODE Blacklist</a> - comprehensive set of regions that have anomalous,
 unstructured or high signal in next-generation sequencing experiments.</li>
 <li>
 <a href="https://www.ncbi.nlm.nih.gov/variation/tools/get-rm/">NCBI GeT-RM</a> - highly homologous
 gene and exon level regions that are difficult or impossible to analyze with standard Sanger or NGS
 approaches and are relevant to current clinical testing.</li>
 <li>
 <a href="https://www.nist.gov/programs-projects/genome-bottle">Genome-in-a-Bottle</a> - defined
 regions where it is difficult to make a confident call, due to low coverage, systematic sequencing
 errors, local alignment problems, etc.</li>
 </ul>
-</p>
 
 <p>
 We would like to thank Anna Benet-Pages, Max Haeussler, Angie Hinrichs, and Daniel Schmelter at the
 UCSC Genome Browser for planning, building, and testing these tracks.
 </p>
 
 <a name="050420"></a>
 <h2>May 4, 2020 &nbsp;&nbsp; May 4th data release for SARS-CoV-2 genome browser</h2>
 <p>
 We are pleased to announce our second data release for the <a target="_blank" 
 href="/cgi-bin/hgTracks?db=wuhCor1">coronavirus genome browser</a>. Much like our 
 <a href="#040320">first release</a>, this includes a variety of annotation types such as CRISPR 
 tracks, protein structure and interaction tracks, immunology tracks, and a 119-way multiple 
 sequence alignment.</p>
 <p>