ParseCNV2: a versatile and integrated tool for copy number variation association studies.

Eur J Hum Genet

Division of Nephrology, Department of Medicine, Columbia University, New York, NY, USA.

Published: March 2023

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995335PMC
http://dx.doi.org/10.1038/s41431-022-01280-xDOI Listing

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