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Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data

Although whole-genome association studies using tagSNPs are a powerful approach for detecting common variants, they are underpowered for detecting associations with rare variants. Recent studies have demonstrated that common diseases can be due to functional variants with a wide spectrum of allele f...

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Detalhes bibliográficos
Main Authors: Li, Bingshan, Leal, Suzanne M.
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2008
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2842185/
https://ncbi.nlm.nih.gov/pubmed/18691683
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2008.06.024
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