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 "All SNPs (146)". 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> + "clinically associated".</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 "Variation" 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.