Genome-Wide Testing of Putative Functional Exonic Variants in Relationship with Breast and Prostate Cancer Risk in a Multiethnic Population

Rare variation in protein coding sequence is poorly captured by GWAS arrays and has been hypothesized to contribute to disease heritability. Using the Illumina HumanExome SNP array, we successfully genotyped 191,032 common and rare non-synonymous, splice site, or nonsense variants in a multiethnic s...

ver descrição completa

Na minha lista:
Detalhes bibliográficos
Main Authors: Haiman, Christopher A., Han, Ying, Feng, Ye, Xia, Lucy, Hsu, Chris, Sheng, Xin, Pooler, Loreall C., Patel, Yesha, Kolonel, Laurence N., Carter, Erin, Park, Karen, Le Marchand, Loic, Van Den Berg, David, Henderson, Brian E., Stram, Daniel O.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2013
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3610631/
https://ncbi.nlm.nih.gov/pubmed/23555315
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1003419
Tags: Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!

Registos relacionados