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L
Li, Heng
Broad Institute, Medical Population Genetics Program, Cambridge, MA, USA
Papers
(2)
Affiliations
(1)
Co-authors
(23)
Title
Year
PMID
Extremely low-coverage sequencing and imputation increases power for genome-wide association studies.
2012
22610117
A statistical framework for SNP calling, mutation discovery, association mapping and population genetical parameter estimation from sequencing data.
2011
21903627
Showing 1–2 of 2
Resolved affiliation
Broad Institute, Medical Population Genetics Program, Cambridge, MA, USA
Raw imported affiliations (1)
Affiliation
Medical Population Genetics Program, Broad Institute, 7 Cambridge Center, Cambridge, MA 02142, USA. hengli@broadinstitute.org
Name
Shared papers
Bergen, Sarah
1
Daly, Mark J
1
de Bakker, Paul I W
1
Garimella, Kiran
1
Gupta, Namrata
1
Haas, David W
1
Hultman, Christina M
1
Liang, Liming
1
Lichtenstein, Paul
1
Magnusson, Patrik
1
McLaren, Paul J
1
Moran, Jennifer L
1
Neale, Benjamin M
1
Pasaniuc, Bogdan
1
Patterson, Nick
1
Price, Alkes L
1
Purcell, Shaun M
1
Reich, David
1
Rohland, Nadin
1
Sklar, Pamela
1
Sullivan, Patrick F
1
Sunyaev, Shamil
1
Zaitlen, Noah
1