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Discovery of Rare Variants via Sequencing: Implications for the Design of Complex Trait Association Studies

There is strong evidence that rare variants are involved in complex disease etiology. The first step in implicating rare variants in disease etiology is their identification through sequencing in both randomly ascertained samples (e.g., the 1,000 Genomes Project) and samples ascertained according to...

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Detaylı Bibliyografya
Asıl Yazarlar: Li, Bingshan, Leal, Suzanne M.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: Public Library of Science 2009
Konular:
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC2674213/
https://ncbi.nlm.nih.gov/pubmed/19436704
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1000481
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