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

Pasaniuc B, Rohland N, McLaren PJ, Garimella K, Zaitlen N, Li H, Gupta N, Neale BM, Daly MJ, Sklar P, Sullivan PF, Bergen S, Moran JL, Hultman CM, Lichtenstein P, Magnusson P, Purcell SM, Haas DW, Liang L, Sunyaev S, Patterson N, de Bakker PI, Reich D, Price AL
Nat Genet. 2012 44 (6): 631-5

PMID: 22610117 · PMCID: PMC3400344 · DOI:10.1038/ng.2283

MeSH Terms (5)

Exome Genome-Wide Association Study Humans Polymorphism, Single Nucleotide Sequence Analysis, DNA

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