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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Detaylı Bibliyografya
Yayımlandı:Genet Epidemiol
Asıl Yazarlar: 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
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: John Wiley and Sons Inc. 2020
Konular:
Research Articles
Online Erişim: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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