Imputation of coding variants in African Americans: better performance using data from the exome sequencing project

Summary: Although the 1000 Genomes haplotypes are the most commonly used reference panel for imputation, medical sequencing projects are generating large alternate sets of sequenced samples. Imputation in African Americans using 3384 haplotypes from the Exome Sequencing Project, compared with 2184 h...

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Detalhes bibliográficos
Main Authors: Duan, Qing, Liu, Eric Yi, Auer, Paul L., Zhang, Guosheng, Lange, Ethan M., Jun, Goo, Bizon, Chris, Jiao, Shuo, Buyske, Steven, Franceschini, Nora, Carlson, Chris S., Hsu, Li, Reiner, Alex P., Peters, Ulrike, Haessler, Jeffrey, Curtis, Keith, Wassel, Christina L., Robinson, Jennifer G., Martin, Lisa W., Haiman, Christopher A., Le Marchand, Loic, Matise, Tara C., Hindorff, Lucia A., Crawford, Dana C., Assimes, Themistocles L., Kang, Hyun Min, Heiss, Gerardo, Jackson, Rebecca D., Kooperberg, Charles, Wilson, James G., Abecasis, Gonçalo R., North, Kari E., Nickerson, Deborah A., Lange, Leslie A., Li, Yun
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
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Original Papers
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3799474/
https://ncbi.nlm.nih.gov/pubmed/23956302
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/bioinformatics/btt477
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