Mid-pass whole genome sequencing enables biomedical genetic studies of diverse populations

Abstract Background Historically, geneticists have relied on genotyping arrays and imputation to study human genetic variation. However, an underrepresentation of diverse populations has resulted in arrays that poorly capture global genetic variation, and a lack of reference panels. This has contrib...

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Auteurs principaux: Anne-Katrin Emde, Amanda Phipps-Green, Murray Cadzow, C. Scott Gallagher, Tanya J. Major, Marilyn E. Merriman, Ruth K. Topless, Riku Takei, Nicola Dalbeth, Rinki Murphy, Lisa K. Stamp, Janak de Zoysa, Philip L. Wilcox, Keolu Fox, Kaja A. Wasik, Tony R. Merriman, Stephane E. Castel
Format: article
Langue:EN
Publié: BMC 2021
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Accès en ligne:https://doaj.org/article/295efebb8290477c8a164ca0f7d5bfec
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