Article
Evaluating the accuracy of a functional SNP annotation system.
BMC bioinformatics - 17 Sept 2009
Shen Terry H, Carlson Christopher S, Tarczy-Hornoch Peter
Abstract excerpt
Many common and chronic diseases are influenced at some level by genetic variation. Research done in population genetics, specifically in the area of single nucleotide polymorphisms (SNPs) is critical to understanding human genetic variation. A key element in assessing role of a given SNP is determining if the variation is likely to result in change in function. The SNP Integration Tool (SNPit) is a comprehensive...
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.