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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
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