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Long-read whole genome sequencing identifies causal structural variation in a Mendelian disease
View ORCID ProfileJason D. Merker, Aaron M. Wenger, Tam Sneddon, Megan Grove, Daryl Waggott, Sowmi Utiramerur, Yanli Hou, Christine C. Lambert, Kevin S. Eng, Luke Hickey, Jonas Korlach, James Ford, Euan A. Ashley
doi: https://doi.org/10.1101/090985
Jason D. Merker
1Department of Pathology, Stanford University, Stanford, California, 94305, USA
2Clinical Genomics Service, Stanford Health Care, Stanford, California, 94305, USA
Aaron M. Wenger
3Pacific Biosciences, Menlo Park, California, 94025, USA
Tam Sneddon
2Clinical Genomics Service, Stanford Health Care, Stanford, California, 94305, USA
Megan Grove
2Clinical Genomics Service, Stanford Health Care, Stanford, California, 94305, USA
Daryl Waggott
4Department of Medicine, Stanford University, Stanford, California, 94305, USA
5Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, 94305, USA
Sowmi Utiramerur
2Clinical Genomics Service, Stanford Health Care, Stanford, California, 94305, USA
Yanli Hou
1Department of Pathology, Stanford University, Stanford, California, 94305, USA
Christine C. Lambert
3Pacific Biosciences, Menlo Park, California, 94025, USA
Kevin S. Eng
3Pacific Biosciences, Menlo Park, California, 94025, USA
Luke Hickey
3Pacific Biosciences, Menlo Park, California, 94025, USA
Jonas Korlach
3Pacific Biosciences, Menlo Park, California, 94025, USA
James Ford
4Department of Medicine, Stanford University, Stanford, California, 94305, USA
6Department of Genetics, Stanford University, Stanford, California, 94305, USA
7Stanford Cancer Institute, Stanford, California, 94305, USA
Euan A. Ashley
2Clinical Genomics Service, Stanford Health Care, Stanford, California, 94305, USA
4Department of Medicine, Stanford University, Stanford, California, 94305, USA
5Stanford Center for Inherited Cardiovascular Disease, Stanford University, Stanford, California, 94305, USA
6Department of Genetics, Stanford University, Stanford, California, 94305, USA
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Posted December 02, 2016.
Long-read whole genome sequencing identifies causal structural variation in a Mendelian disease
Jason D. Merker, Aaron M. Wenger, Tam Sneddon, Megan Grove, Daryl Waggott, Sowmi Utiramerur, Yanli Hou, Christine C. Lambert, Kevin S. Eng, Luke Hickey, Jonas Korlach, James Ford, Euan A. Ashley
bioRxiv 090985; doi: https://doi.org/10.1101/090985
Long-read whole genome sequencing identifies causal structural variation in a Mendelian disease
Jason D. Merker, Aaron M. Wenger, Tam Sneddon, Megan Grove, Daryl Waggott, Sowmi Utiramerur, Yanli Hou, Christine C. Lambert, Kevin S. Eng, Luke Hickey, Jonas Korlach, James Ford, Euan A. Ashley
bioRxiv 090985; doi: https://doi.org/10.1101/090985
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