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.
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