ParseCNV2: a versatile and integrated tool for copy number variation association studies
Eur J Hum Genet
.
2023 Mar;31(3):275-277.
doi: 10.1038/s41431-022-01280-x.
Epub 2023 Jan 11.
Authors
Tze Y Lim
1
,
Miguel Verbitsky
1
,
Simone Sanna-Cherchi
2
Affiliations
1
Division of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.
2
Division of Nephrology, Department of Medicine, Columbia University, New York, NY, USA. ss2517@cumc.columbia.edu.
PMID:
36631543
PMCID:
PMC9995335
DOI:
10.1038/s41431-022-01280-x
No abstract available
Publication types
Research Support, N.I.H., Extramural
Comment
MeSH terms
DNA Copy Number Variations*
Gene Dosage
Genome-Wide Association Study*
Humans
Grants and funding
P20 DK116191/DK/NIDDK NIH HHS/United States
R01 DK103184/DK/NIDDK NIH HHS/United States
R01 DK115574/DK/NIDDK NIH HHS/United States