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Is it rare or common?

Many Genome-Wide Association Studies (GWAS) have signals with unknown etiology. This paper addresses the question — is such an association signal caused by rare or common variants that lead to increased disease risk? For a genomic region implicated by a GWAS, we use Single Nucleotide Polymorphism (S...

詳細記述

保存先:
書誌詳細
主要な著者: Adhikari, Kaustubh, AlChawa, Taofik, Ludwig, Kerstin, Laird, Nan, Mangold, Elisabeth, Lange, Christoph
フォーマット: Artigo
言語:Inglês
出版事項: 2012
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC3641852/
https://ncbi.nlm.nih.gov/pubmed/22549767
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.21637
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