0c12430b872310f016b018db863d09697dc4deaf
gperez2
  Tue Jan 26 11:49:25 2021 -0800
Code review edits to gnomAD track announcement, updated CGI links, and uncapitalized words, refs #26858

diff --git src/hg/htdocs/goldenPath/newsarch.html src/hg/htdocs/goldenPath/newsarch.html
index 6a09479..9dacfa4 100755
--- src/hg/htdocs/goldenPath/newsarch.html
+++ src/hg/htdocs/goldenPath/newsarch.html
@@ -82,50 +82,48 @@
 <ul>
   <li><a href="../goldenPath/credits.html#dog_use" 
 target="_blank" >Data use conditions and restrictions</a></li>
   <li><a href="../goldenPath/help/ftp.html" 
 target="_blank" >Rsync</a> and
 <a href="ftp://hgdownload.soe.ucsc.edu/goldenPath/canFam5/" 
 target="_blank" >FTP</a></li>
   <li><a href="http://hgdownload.soe.ucsc.edu/downloads.html#dog"
 target="_blank" >Downloads page</a></li>
 </ul>
 </p>
 
 <a name="012221"></a>
 <h2>Jan. 22, 2021 &nbsp;&nbsp; Updates to gnomAD variation track (GRCh37/hg19)(GRCh38/hg38)</h2>
 <p>
-We are pleased to announce updates to the
-<a href="../../cgi-bin/hgTrackUi?db=hg38&c=chr22&g=gnomadVariants"
-target="_blank">gnomAD Variants super-track</a> for the <a target="_blank"
-href="../../cgi-bin/hgTrackUi?db=hg19&c=chrX&g=gnomadSuper">hg19/GRCh37</a>
+We are pleased to announce updates to the gnomAD Variants super-track for the <a target="_blank"
+href="/cgi-bin/hgTrackUi?db=hg19&c=chrX&g=gnomadSuper">hg19/GRCh37</a>
 and <a target="_blank"
-href="../../cgi-bin/hgTrackUi?db=hg38&c=chrX&g=gnomadVariants">hg38/GRCh38</a>
+href="/cgi-bin/hgTrackUi?db=hg38&c=chrX&g=gnomadVariants">hg38/GRCh38</a>
 human assemblies.</p>
 <ul>
   <li>gnomAD v3.1 is now available and contains variants from 76,156 whole genomes (and no exomes),
       all mapped to the GRCh38/hg38 reference sequence. 4,454 genomes were added to the number of
       genomes in the previous v3 release. For more detailed information on gnomAD v3.1, see the related
       <a href="https://gnomad.broadinstitute.org/blog/2020-10-gnomad-v3-1/"target="_blank">blog post</a>.</li>
   <li>The latest release (gnomAD 2.1.1) is also available for GRCh37/hg19 genome assembly. This release
       contains variant data for 125,748 exomes and 15,708 whole genomes.</li>
   <li>Three filters are now available for our updated v2.1.1 (GRCh37/hg19) and gnomAD v3.1 (GRCh38/hg38) tracks,
       by minor allele frequency (MAF), quality tags, annotation type, and variant type.</li>
   <li>Mouse hover over now displays details about each variant, including the affected gene(s), the variant type,
       and annotation.</li>
-  <li>Following the conventions on the gnomAD browser, items are shaded according to their Annotation type: pLoF
-      is red, Missense is orange, Synonymous is green, and Others are black.</li></ul>
+  <li>Following the conventions on the gnomAD browser, items are shaded according to their annotation type: pLoF
+      is red, missense is orange, synonymous is green, and others are black.</li></ul>
 <p class="text-center">
   <img class='text-center' src="../images/gnomadV3_1.jpg"  width='100%' alt="The gnomAD v3.1 track display.">
 </p>
 
 <p>
 We would like to thank the <a target="_blank" href="http://gnomad.broadinstitute.org/">Genome Aggregation Database
 (gnomAD)</a> team at the BROAD institute and the UCSC Genome Browser team members Christopher Lee, Anna Benet-Pages,
 Daniel Schmelter, and Gerardo Perez for developing and releasing these tracks.</p>
 
 
 <a name="011321"></a>
 <h2>Jan. 13, 2021 &nbsp;&nbsp; New GENCODE gene tracks: Human V35/V36 (hg19/hg38)</h2>
 <p>
 We are pleased to announce new GENCODE Gene annotation tracks, which correspond
 to <a href="http://www.ensembl.info/2020/08/20/ensembl-101-has-been-released/"