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Indexcov: fast coverage quality control for whole-genome sequencing
Brent S. Pedersen, Ryan L. Collins, Michael E. Talkowski, Aaron R. Quinlan
doi: https://doi.org/10.1101/148296
Brent S. Pedersen
1Department of Human Genetics, University of Utah, Salt Lake City, UT
3USTAR Center for Genetic Discovery, University of Utah, Salt Lake City, UT
Ryan L. Collins
4Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA
6Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA
7Program in Bioinformatics and Integrative Genomics, Division of Medical Sciences, Harvard Medical School, Boston, MA.
Michael E. Talkowski
4Center for Genomic Medicine, Massachusetts General Hospital, Boston, MA
5Department of Neurology, Harvard Medical School, Boston, MA
6Program in Medical and Population Genetics and Stanley Center for Psychiatric Research, Broad Institute, Cambridge, MA
7Program in Bioinformatics and Integrative Genomics, Division of Medical Sciences, Harvard Medical School, Boston, MA.
Aaron R. Quinlan
1Department of Human Genetics, University of Utah, Salt Lake City, UT
2Department of Biomedical Informatics, University of Utah, Salt Lake City, UT
3USTAR Center for Genetic Discovery, University of Utah, Salt Lake City, UT
Article usage
Posted June 09, 2017.
Indexcov: fast coverage quality control for whole-genome sequencing
Brent S. Pedersen, Ryan L. Collins, Michael E. Talkowski, Aaron R. Quinlan
bioRxiv 148296; doi: https://doi.org/10.1101/148296
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