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 @@

Common SNPs (142): uniquely mapped variants that appear in at least 1% of the population or are 100% non-reference

Flagged SNPs (142): uniquely mapped variants, excluding Common SNPs, that have been flagged by dbSNP as "clinically associated"

Mult. SNPs (142): variants that have been mapped to more than one genomic location

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.

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.

+ 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 + preview server, + and the associated masked FASTA files will continue to be available on our + download server. +

2 Febuary 2015 - Host a Genome Browser Workshop

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.

For more information or to submit a request to host a workshop, please visit our signup.