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Association score testing for rare variants and binary traits in family data with shared controls

Genome-wide association studies have been an important approach used to localize trait loci, with primary focus on common variants. The multiple rare variant–common disease hypothesis may explain the missing heritability remaining after accounting for identified common variants. Advances of sequenci...

詳細記述

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書誌詳細
出版年:Brief Bioinform
主要な著者: Saad, Mohamad, Wijsman, Ellen M
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2017
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC6357552/
https://ncbi.nlm.nih.gov/pubmed/28968627
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bib/bbx107
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