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De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families
View ORCID ProfileJonathan R. Belyeu, View ORCID ProfileHarrison Brand, Harold Wang, View ORCID ProfileXuefang Zhao, View ORCID ProfileBrent S. Pedersen, View ORCID ProfileJulie Feusier, Meenal Gupta, Thomas J. Nicholas, Lisa Baird, View ORCID ProfileBernie Devlin, View ORCID ProfileStephan J. Sanders, View ORCID ProfileLynn B. Jorde, View ORCID ProfileMichael E. Talkowski, View ORCID ProfileAaron R. Quinlan
doi: https://doi.org/10.1101/2020.10.06.329011
Jonathan R. Belyeu
1Department of Human Genetics, University of Utah, Salt Lake City, UT
Harrison Brand
2Center for Genomic Medicine, Massachusetts General Hospital, Boston MA
3Department of Neurology, Harvard Medical School, Boston MA
4Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge MA
Harold Wang
2Center for Genomic Medicine, Massachusetts General Hospital, Boston MA
3Department of Neurology, Harvard Medical School, Boston MA
4Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge MA
Xuefang Zhao
2Center for Genomic Medicine, Massachusetts General Hospital, Boston MA
3Department of Neurology, Harvard Medical School, Boston MA
4Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge MA
Brent S. Pedersen
1Department of Human Genetics, University of Utah, Salt Lake City, UT
Julie Feusier
5Huntsman Cancer Institute, University of Utah, Salt Lake City, UT
Meenal Gupta
1Department of Human Genetics, University of Utah, Salt Lake City, UT
Thomas J. Nicholas
1Department of Human Genetics, University of Utah, Salt Lake City, UT
Lisa Baird
1Department of Human Genetics, University of Utah, Salt Lake City, UT
Bernie Devlin
6Department of Psychiatry, University of Pittsburgh School of Medicine, Pittsburgh, PA 15213, USA
Stephan J. Sanders
7Department of Psychiatry, UCSF Weill Institute for Neurosciences, University of California, San Francisco, CA, USA
8Institute for Human Genetics, University of California, San Francisco, CA, USA
Lynn B. Jorde
1Department of Human Genetics, University of Utah, Salt Lake City, UT
10Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT
Michael E. Talkowski
2Center for Genomic Medicine, Massachusetts General Hospital, Boston MA
3Department of Neurology, Harvard Medical School, Boston MA
4Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute of Harvard and MIT, Cambridge MA
Aaron R. Quinlan
1Department of Human Genetics, University of Utah, Salt Lake City, UT
9Department of Biomedical Informatics, University of Utah, Salt Lake City, UT
10Utah Center for Genetic Discovery, University of Utah, Salt Lake City, UT
Posted October 08, 2020.
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families
Jonathan R. Belyeu, Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier, Meenal Gupta, Thomas J. Nicholas, Lisa Baird, Bernie Devlin, Stephan J. Sanders, Lynn B. Jorde, Michael E. Talkowski, Aaron R. Quinlan
bioRxiv 2020.10.06.329011; doi: https://doi.org/10.1101/2020.10.06.329011
De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families
Jonathan R. Belyeu, Harrison Brand, Harold Wang, Xuefang Zhao, Brent S. Pedersen, Julie Feusier, Meenal Gupta, Thomas J. Nicholas, Lisa Baird, Bernie Devlin, Stephan J. Sanders, Lynn B. Jorde, Michael E. Talkowski, Aaron R. Quinlan
bioRxiv 2020.10.06.329011; doi: https://doi.org/10.1101/2020.10.06.329011
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