regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions

Motivation: One of the fundamental questions in genetics study is to identify functional DNA variants that are responsible to a disease or phenotype of interest. Results from large-scale genetics studies, such as genome-wide association studies (GWAS), and the availability of high-throughput sequenc...

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Detalhes bibliográficos
Main Authors: Teng, Mingxiang, Ichikawa, Shoji, Padgett, Leah R., Wang, Yadong, Mort, Matthew, Cooper, David N., Koller, Daniel L., Foroud, Tatiana, Edenberg, Howard J., Econs, Michael J., Liu, Yunlong
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2012
Assuntos:
Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3389767/
https://ncbi.nlm.nih.gov/pubmed/22611130
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/bts275
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