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Improving accuracy of rare variant imputation with a two-step imputation approach

Genotype imputation has been the pillar of the success of genome-wide association studies (GWAS) for identifying common variants associated with common diseases. However, most GWAS have been run using only 60 HapMap samples as reference for imputation, meaning less frequent and rare variants not bei...

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Detalles Bibliográficos
Publicado en:Eur J Hum Genet
Main Authors: Kreiner-Møller, Eskil, Medina-Gomez, Carolina, Uitterlinden, André G, Rivadeneira, Fernando, Estrada, Karol
Formato: Artigo
Idioma:Inglês
Publicado: Nature Publishing Group 2015
Assuntos:
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC4326719/
https://ncbi.nlm.nih.gov/pubmed/24939589
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2014.91
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