SCAN: SNP and copy number annotation

Motivation: Genome-wide association studies (GWAS) generate relationships between hundreds of thousands of single nucleotide polymorphisms (SNPs) and complex phenotypes. The contribution of the traditionally overlooked copy number variations (CNVs) to complex traits is also being actively studied. T...

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Autors principals: Gamazon, Eric R., Zhang, Wei, Konkashbaev, Anuar, Duan, Shiwei, Kistner, Emily O., Nicolae, Dan L., Dolan, M. Eileen, Cox, Nancy J.
Format: Artigo
Idioma:Inglês
Publicat: Oxford University Press 2010
Matèries:
Original Papers
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC2852202/
https://ncbi.nlm.nih.gov/pubmed/19933162
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btp644
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