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Linked-read analysis identifies mutations in single cell DNA sequencing data
Craig L. Bohrson, Allison R. Barton, Michael A. Lodato, Rachel E. Rodin, Vinay Viswanadham, Doga Gulhan, Isidro Cortes, Maxwell A. Sherman, Lovelace J. Luquette, Minseok Kwon, Michael E. Coulter, Christopher A. Walsh, Peter J. Park
doi: https://doi.org/10.1101/211169
Craig L. Bohrson
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
2Bioinformatics and Integrative Genomics PhD program, Harvard Medical School, Boston, MA, USA
Allison R. Barton
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
2Bioinformatics and Integrative Genomics PhD program, Harvard Medical School, Boston, MA, USA
Michael A. Lodato
4Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, MA, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA
Rachel E. Rodin
4Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, MA, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA
5Program in Neuroscience and Harvard/MIT MD-PHD Program, Harvard Medical School (HMS), Boston, MA
Vinay Viswanadham
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
2Bioinformatics and Integrative Genomics PhD program, Harvard Medical School, Boston, MA, USA
Doga Gulhan
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
Isidro Cortes
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
3Centre for Molecular Science Informatics, Department of Chemistry, University of Cambridge, Lensfield Road, Cambridge CB2 1EW, United Kingdom
Maxwell A. Sherman
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
Lovelace J. Luquette
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
2Bioinformatics and Integrative Genomics PhD program, Harvard Medical School, Boston, MA, USA
Minseok Kwon
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
Michael E. Coulter
4Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, MA, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA
5Program in Neuroscience and Harvard/MIT MD-PHD Program, Harvard Medical School (HMS), Boston, MA
Christopher A. Walsh
4Division of Genetics and Genomics, Manton Center for Orphan Disease, and Howard Hughes Medical Institute, Boston Children's Hospital, Boston, MA, USA; Departments of Neurology and Pediatrics, Harvard Medical School, Boston, MA, USA; Broad Institute of MIT and Harvard, Cambridge, MA, USA
Peter J. Park
1Department of Biomedical Informatics, Harvard Medical School, Boston, MA, USA
Article usage
Posted October 30, 2017.
Linked-read analysis identifies mutations in single cell DNA sequencing data
Craig L. Bohrson, Allison R. Barton, Michael A. Lodato, Rachel E. Rodin, Vinay Viswanadham, Doga Gulhan, Isidro Cortes, Maxwell A. Sherman, Lovelace J. Luquette, Minseok Kwon, Michael E. Coulter, Christopher A. Walsh, Peter J. Park
bioRxiv 211169; doi: https://doi.org/10.1101/211169
Linked-read analysis identifies mutations in single cell DNA sequencing data
Craig L. Bohrson, Allison R. Barton, Michael A. Lodato, Rachel E. Rodin, Vinay Viswanadham, Doga Gulhan, Isidro Cortes, Maxwell A. Sherman, Lovelace J. Luquette, Minseok Kwon, Michael E. Coulter, Christopher A. Walsh, Peter J. Park
bioRxiv 211169; doi: https://doi.org/10.1101/211169
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