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A Groupwise Association Test for Rare Mutations Using a Weighted Sum Statistic

Resequencing is an emerging tool for identification of rare disease-associated mutations. Rare mutations are difficult to tag with SNP genotyping, as genotyping studies are designed to detect common variants. However, studies have shown that genetic heterogeneity is a probable scenario for common di...

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Detalhes bibliográficos
Main Authors: Madsen, Bo Eskerod, Browning, Sharon R.
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2009
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2633048/
https://ncbi.nlm.nih.gov/pubmed/19214210
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000384
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