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Identification of rare variants for hypertension with incorporation of linkage information

We conducted linkage analysis using the genome-wide association study data on chromosome 3, and then assessed association between hypertension and rare variants of genes located in the regions showing evidence of linkage. The rare variants were collapsed if their minor allele frequencies were less t...

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Detalhes bibliográficos
Main Authors: Chiu, Yen-Feng, Chung, Ren-Hua, Lee, Chun-Yi, Kao, Hui-Yi, Hou, Lin, Hsu, Fang-Chi
Formato: Artigo
Idioma:Inglês
Publicado em: BioMed Central 2014
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC4144469/
https://ncbi.nlm.nih.gov/pubmed/25519312
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1753-6561-8-S1-S109
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