Keeping up with the genomes: scaling genomic variant interpretation
Genome Med
.
2019 Dec 31;12(1):5.
doi: 10.1186/s13073-019-0700-4.
Authors
Heidi L Rehm
1
2
3
,
Douglas M Fowler
4
5
6
Affiliations
1
Center for Genomic Medicine, Massachusetts General Hospital, Cambridge Street, Boston, MA, 02114, USA. hrehm@mgh.harvard.edu.
2
Medical and Population Genetics, Broad Institute of MIT and Harvard, Main Street, Cambridge, MA, 02142, USA. hrehm@mgh.harvard.edu.
3
Department of Pathology, Harvard Medical School, Shattuck Street, Boston, MA, 02115, USA. hrehm@mgh.harvard.edu.
4
Department of Genome Sciences, University of Washington, 15th Avenue NE, Seattle, WA, 98195-5065, USA. dfowler@uw.edu.
5
Canadian Institute for Advanced Research, University Avenue, Toronto, ON, M5G 1M1, Canada. dfowler@uw.edu.
6
Department of Bioengineering, University of Washington, 15th Avenue NE, Seattle, WA, 98195-5061, USA. dfowler@uw.edu.
PMID:
31892366
PMCID:
PMC6938604
DOI:
10.1186/s13073-019-0700-4
No abstract available
Publication types
Editorial
Introductory Journal Article
Research Support, N.I.H., Extramural
MeSH terms
Genetic Loci
Genetic Variation*
Genome, Human*
Humans
Neoplasms / genetics
Neoplasms / pathology
Grants and funding
RM1 HG010461/HG/NHGRI NIH HHS/United States
U41 HG006834/HG/NHGRI NIH HHS/United States
R01 GM109110/GM/NIGMS NIH HHS/United States
UM1 HG008900/HG/NHGRI NIH HHS/United States
U01 HG008676/HG/NHGRI NIH HHS/United States