Optimal Haplotype Block-Free Selection of Tagging SNPs for Genome-Wide Association Studies

It is widely hoped that the study of sequence variation in the human genome will provide a means of elucidating the genetic component of complex diseases and variable drug responses. A major stumbling block to the successful design and execution of genome-wide disease association studies using singl...

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Опубликовано в::	Genome Res
Главные авторы:	Halldórsson, Bjarni V., Bafna, Vineet, Lippert, Ross, Schwartz, Russell, De La Vega, Francisco M., Clark, Andrew G., Istrail, Sorin
Формат:	Artigo
Язык:	Inglês
Опубликовано:	Cold Spring Harbor Laboratory Press 2004
Предметы:	Methods
Online-ссылка:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC509273/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/15289481/ https://ncbi.nlm.nih.govhttps://doi.org/10.1101/gr.2570004
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