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Paper Details

Extent to which array genotyping and imputation with large reference panels approximate deep whole-genome sequencing.
Am J Hum Genet
10
2022
1000G, HRC, Illumina Core, MEGA, Omni 2, OmniExpress, SNVs, bi-allelic single-nucleotide variants, genetic variants, genomic region, genomic regions, human, indel
Author NameAffiliation
Ryan P WelchDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan ann arbor
Eimear E KennyIcahn School of Medicine at Mount Sinai, USA Institute for Genomic Health
Eimear E KennyIcahn School of Medicine at Mount Sinai, USA Institute for Genomic Health
Markku LaaksoUniversity of Eastern Finland
Ruth J F LoosCharles Bronfman Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai
Steven A McCarrollStanley Center for Psychiatric Research, Broad Institute of MIT and Harvard, Harvard Medical School
Carlos N PatoRutgers University, Robert Wood Johnson Medical School and New Jersey Medical School
Michele T PatoRutgers University, Robert Wood Johnson Medical School and New Jersey Medical School
Albert V SmithDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan ann arbor
Albert V SmithDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan ann arbor
Michael BoehnkeDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan ann arbor
Laura J ScottDepartment of Biostatistics and Center for Statistical Genetics, School of Public Health, University of Michigan ann arbor
Christian FuchsbergerInstitute for Biomedicine (Affiliated with the University of Lubeck)
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