Extremely low-coverage sequencing and imputation increases power for genome-wide association studies

Genome wide association studies (GWAS) have proven a powerful method to identify common genetic variants contributing to susceptibility to common diseases. Here we show that extremely low-coverage sequencing (0.1–0.5x) captures almost as much of the common (>5%) and low-frequency (1–5%) variation...

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Detaylı Bibliyografya
Asıl Yazarlar: Pasaniuc, Bogdan, Rohland, Nadin, McLaren, Paul J., Garimella, Kiran, Zaitlen, Noah, Li, Heng, Gupta, Namrata, Neale, Benjamin, Daly, Mark, Sklar, Pamela, Sullivan, Patrick F., Bergen, Sarah, Moran, Jennifer L., Hultman, Christina M., Lichtenstein, Paul, Magnusson, Patrik, Purcell, Shaun M., Haas, David W., Liang, Liming, Sunyaev, Shamil, Patterson, Nick, de Bakker, Paul I.W., Reich, David, Price, Alkes L.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2012
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC3400344/
https://ncbi.nlm.nih.gov/pubmed/22610117
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ng.2283
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