f129240578e8fc0849c53ddace9c0fb43535eebf
mspeir
  Fri Apr 15 14:53:59 2016 -0700
HTML encoding quotes in announcement, refs #16777

diff --git src/hg/htdocs/indexNews.html src/hg/htdocs/indexNews.html
index b6f8a50..6fb09c1 100755
--- src/hg/htdocs/indexNews.html
+++ src/hg/htdocs/indexNews.html
@@ -76,43 +76,43 @@
   </p>
 
   <p>
   There are four SNP tracks available as part of this release.
   One is a track containing all mappings of reference SNPs
   to the human assembly, labeled &quot;All SNPs (146)&quot;.
   The other three tracks are subsets of this track
   and show interesting and easily defined subsets of dbSNP:
   </p>
 
   <ul>
   <li>Common SNPs (146): uniquely mapped variants that appear
   in at least 1% of the population or are 100% non-reference.</li>
   <li>Flagged SNPs (146): uniquely mapped variants, excluding
   Common SNPs, that have been flagged by dbSNP as
-  "clinically associated".</li>
+  &quot;clinically associated&quot;.</li>
   <li>Mult. SNPs (146): variants that have been mapped to more
   than one genomic location. This track has been shrinking over
   the course of the last few releases as dbSNP now excludes most
   SNPs whose flanking sequences map to multiple locations in
   the genome.</li>
   </ul>
 
   <p>
   By default, only the Common SNPs (146) are visible;
   other tracks must be made visible using the track controls.
   You will find the other SNPs (146) tracks on both
-  of GRCh37/hg19 and GRCh38/hg38 browsers in the "Variation" group.
+  of GRCh37/hg19 and GRCh38/hg38 browsers in the &quot;Variation&quot; group.
   </p>
   <p>
   The tracks were produced at UCSC by Angie Hinrichs and
   Matthew Speir. We'd like to thank the dbSNP group at
   NCBI for providing access to these data.
   </p>
 
   <hr>
   <a name="041516"></a>
   <p>
   <font color="#006666" size="4"><b> 15 April 2016 -
   Three New Assemblies Now Available in the Genome Browser</b></font>
   <p>
   A Genome Browser is now available for the gorilla (<em>Gorilla gorilla gorilla</em>)
   assembly released December 2014 by the Wellcome Trust Sanger Institute.