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Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders
Robert Brown, Hane Lee, Ascia Eskin, Gleb Kichaev, Kirk E. Lohmueller, Bruno Reversade, Stanley F. Nelson, Bogdan Pasaniuc
doi: https://doi.org/10.1101/010017
Robert Brown
1Bioinformatics Interdepartmental Program, University of California Los Angeles, Los Angeles California, USA
Hane Lee
2Department of Pathology and Laboratory Medicine, Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
Ascia Eskin
3Department of Human Genetics, Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
Gleb Kichaev
1Bioinformatics Interdepartmental Program, University of California Los Angeles, Los Angeles California, USA
Kirk E. Lohmueller
1Bioinformatics Interdepartmental Program, University of California Los Angeles, Los Angeles California, USA
4Department of Ecology and Evolutionary Biology, University of California Los Angeles, Los Angeles, California, United States of America
Bruno Reversade
5Institute of Medical Biology, Human Genetics and Embryology Laboratory, A*STAR, Singapore 138648, Singapore
6Institute of Molecular and Cellular Biology, A*STAR, Singapore 138673, Singapore
7Department of Pediatrics, National University of Singapore, Singapore 119260, Singapore
Stanley F. Nelson
2Department of Pathology and Laboratory Medicine, Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
3Department of Human Genetics, Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
Bogdan Pasaniuc
1Bioinformatics Interdepartmental Program, University of California Los Angeles, Los Angeles California, USA
2Department of Pathology and Laboratory Medicine, Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
3Department of Human Genetics, Geffen School of Medicine, University of California Los Angeles, Los Angeles, California, USA
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Posted October 04, 2014.
Leveraging ancestry to improve causal variant identification in exome sequencing for monogenic disorders
Robert Brown, Hane Lee, Ascia Eskin, Gleb Kichaev, Kirk E. Lohmueller, Bruno Reversade, Stanley F. Nelson, Bogdan Pasaniuc
bioRxiv 010017; doi: https://doi.org/10.1101/010017
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