Sunday, November 20, 2011

Fwd: SeattleSeq Annotation

Fwd: please follow footer link
The SeattleSeq Annotation server provides annotation of SNPs (single-nucleotide polymorphisms), both known and novel. This annotation includes dbSNP rs ID, gene names and accession numbers, SNP functions (e.g. missense), protein positions and amino-acid changes, conservation scores, HapMap frequencies, PolyPhen predictions, and clinical association. Links to other annotation sites are also provided. Limited annotation for indels is also available. Data from a number of sources has been pooled to create a local database from which many of the properties are drawn. This is the same database that is used by the Genome Variation Server (GVS). This site is supported by grants from the National Human Genome Research Institute and the National Heart, Lung, and Blood Institute. Please see the terms of service.
(Original Post: SeattleSeq Annotation.)