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A multistep approach to single nucleotide polymorphism–set analysis: an evaluation of power and type I error of gene-based tests of association after pathway-based association tests

The aggregation of functionally associated variants given a priori biological information can aid in the discovery of rare variants associated with complex diseases. Many methods exist that aggregate rare variants into a set and compute a single p value summarizing association between the set of rar...

詳細記述

保存先:
書誌詳細
出版年:BMC Proc
主要な著者: Valcarcel, Alessandra, Grinde, Kelsey, Cook, Kaitlyn, Green, Alden, Tintle, Nathan
フォーマット: Artigo
言語:Inglês
出版事項: BioMed Central 2016
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC5133510/
https://ncbi.nlm.nih.gov/pubmed/27980661
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12919-016-0055-4
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