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ParseCNV2: a versatile and integrated tool for copy number variation association studies
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Year:
2023
Type:
article
Source:
European Journal of Human Genetics
DOI:
10.1038/s41431-022-01280-x
Authors:
Tze Y. Lim,
Miguel Verbitsky,
Simone Sanna-Cherchi
Institutions:
Columbia University,
Columbia University Irving Medical Center
Language:
English
Topic:
Genomic variations and chromosomal abnormalities
Subfield:
Genetics
Field:
Biochemistry, Genetics and Molecular Biology
Domain:
Life Sciences
SDG:
Good health and well-being
Open Access status:
green
Funder:
National Institute of Diabetes and Digestive and Kidney Diseases
Awards:
Genetics of Congenital Obstructive Uropathy,
Novel genomic and transcriptomic tools to study human congenital anomalies of the kidney and urinary tract,
Genomics of mammalian posterior urethral valves
OpenAlex ID:
W4315650264
FWCI:
0.166
Cites:
10
Cited by:
1
Related to:
10