Inferring combined CNV/SNP haplotypes from genotype data

Motivation: Copy number variations (CNVs) are increasingly recognized as an substantial source of individual genetic variation, and hence there is a growing interest in investigating the evolutionary history of CNVs as well as their impact on complex disease susceptibility. CNV/SNP haplotypes are cr...

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Bibliografiske detaljer
Main Authors: Su, Shu-Yi, Asher, Julian E., Jarvelin, Marjo-Riita, Froguel, Phillipe, Blakemore, Alexandra I.F., Balding, David J., Coin, Lachlan J.M.
Format: Artigo
Sprog:Inglês
Udgivet: Oxford University Press 2010
Fag:
Original Papers
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC2913665/
https://ncbi.nlm.nih.gov/pubmed/20406911
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btq157
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