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

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 contributed to...

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Detalles Bibliográficos
Autores principales: Emde, Anne-Katrin, Phipps-Green, Amanda, Cadzow, Murray, Gallagher, C. Scott, Major, Tanya J., Merriman, Marilyn E., Topless, Ruth K., Takei, Riku, Dalbeth, Nicola, Murphy, Rinki, Stamp, Lisa K., de Zoysa, Janak, Wilcox, Philip L., Fox, Keolu, Wasik, Kaja A., Merriman, Tony R., Castel, Stephane E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559369/
https://www.ncbi.nlm.nih.gov/pubmed/34719381
http://dx.doi.org/10.1186/s12864-021-07949-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8559369/
https://www.ncbi.nlm.nih.gov/pubmed/34719381
http://dx.doi.org/10.1186/s12864-021-07949-9

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