96d17c7705425cd776fcdba292c5f62a687daadc jcasper Thu Feb 12 10:54:13 2015 -0800 Adding notice of the retirement of snp135/137 to 142 release, refs #14189 diff --git src/hg/htdocs/indexNews.html src/hg/htdocs/indexNews.html index a6ebe0f..ab1bac0 100755 --- src/hg/htdocs/indexNews.html +++ src/hg/htdocs/indexNews.html @@ -57,30 +57,38 @@ <li>Common SNPs (142): uniquely mapped variants that appear in at least 1% of the population or are 100% non-reference <li>Flagged SNPs (142): uniquely mapped variants, excluding Common SNPs, that have been flagged by dbSNP as "clinically associated" <li>Mult. SNPs (142): variants that have been mapped to more than one genomic location </ul> <p> By default, only the Common SNPs (142) are visible; other tracks must be made visible using the track controls. You will find the other SNPs (142) tracks on both of GRCh37/hg19 and GRCh38/hg38 browsers in the "Variation" group. </p> <p> The tracks were produced at UCSC by Angie Hinrichs and Jonathan Casper. We'd like to thank the dbSNP group at NCBI for providing access to these data. </p> + <p> + As part of this release, we are also retiring the older dbSNP Build 135 and 137 + data from display on the GRCh37/hg19 human assembly. Those tracks will still be + available for viewing on our + <a href="http://genome-preview.soe.ucsc.edu" target="_blank">preview server</a>, + and the associated masked FASTA files will continue to be available on our + <a href="http://hgdownload.soe.ucsc.edu" target="_blank">download server</a>. + </p> <hr> <p> <font face="courier" size="3"><b>2 Febuary 2015 - Host a Genome Browser Workshop</b></font> <p> New timeslots are now available to host a Genome Browser workshop at your institution. Thanks to the funding support of NHGRI, we offer hands-on Genome Browser training onsite at your institution, tailored to your audience's level of expertise. </p> <p> For more information or to submit a request to host a workshop, please visit <a href="http://bit.ly/ucscTraining" target="_blank">our signup</a>. </p> <hr> <p>