Sequencing and imputation in GWAS: Cost‐effective strategies to increase power and genomic coverage across diverse populations

A key aim for current genome‐wide association studies (GWAS) is to interrogate the full spectrum of genetic variation underlying human traits, including rare variants, across populations. Deep whole‐genome sequencing is the gold standard to fully capture genetic variation, but remains prohibitively...

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Detalhes bibliográficos
Publicado no:Genet Epidemiol
Main Authors: Quick, Corbin, Anugu, Pramod, Musani, Solomon, Weiss, Scott T., Burchard, Esteban G., White, Marquitta J., Keys, Kevin L., Cucca, Francesco, Sidore, Carlo, Boehnke, Michael, Fuchsberger, Christian
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2020
Assuntos:
Research Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7449570/
https://ncbi.nlm.nih.gov/pubmed/32519380
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/gepi.22326
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