Publisher Correction: SAIGE-GENE+ improves the efficiency and accuracy of set-based rare variant association tests
Nat Genet
.
2022 Nov;54(11):1755.
doi: 10.1038/s41588-022-01220-x.
Authors
Wei Zhou
#
1
2
3
,
Wenjian Bi
#
4
5
6
,
Zhangchen Zhao
#
7
8
,
Kushal K Dey
9
,
Karthik A Jagadeesh
9
,
Konrad J Karczewski
10
11
12
,
Mark J Daly
10
11
12
13
,
Benjamin M Neale
10
11
12
,
Seunggeun Lee
14
Affiliations
1
Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA. wzhou@broadinstitute.org.
2
Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA. wzhou@broadinstitute.org.
3
Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge, MA, USA. wzhou@broadinstitute.org.
4
Department of Medical Genetics, School of Basic Medical Sciences, Peking University, Beijing, China. wenjianb@pku.edu.cn.
5
Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI, USA. wenjianb@pku.edu.cn.
6
Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI, USA. wenjianb@pku.edu.cn.
7
Center for Statistical Genetics, University of Michigan School of Public Health, Ann Arbor, MI, USA.
8
Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI, USA.
9
Department of Epidemiology, Harvard T. H. Chan School of Public Health, Boston, MA, USA.
10
Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
11
Program in Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
12
Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge, MA, USA.
13
Institute for Molecular Medicine Finland, Helsinki Institute of Life Sciences, University of Helsinki, Helsinki, Finland.
14
Graduate School of Data Science, Seoul National University, Seoul, Korea. lee7801@snu.ac.kr.
#
Contributed equally.
PMID:
36257984
PMCID:
PMC9649418
DOI:
10.1038/s41588-022-01220-x
No abstract available
Publication types
Published Erratum
Grants and funding
2020H1D3A2A03100666/National Research Foundation of Korea (NRF)
T32HG010464/U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI)
K99HG012222/U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI)
K99HG012203/U.S. Department of Health & Human Services | NIH | National Human Genome Research Institute (NHGRI)
R01-HG008773/Foundation for the National Institutes of Health (Foundation for the National Institutes of Health, Inc.)