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

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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Autores principales: 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
Formato: article
Lenguaje:EN
Publicado: BMC 2021
Materias:
Biotechnology
TP248.13-248.65
Genetics
QH426-470
Acceso en línea:https://doaj.org/article/295efebb8290477c8a164ca0f7d5bfec
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https://doaj.org/article/295efebb8290477c8a164ca0f7d5bfec

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