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

Lim, T. Y., Verbitsky, M., & Sanna-Cherchi, S. (2023). ParseCNV2: a versatile and integrated tool for copy number variation association studies. European Journal of Human Genetics, 31(3), 275–277. https://doi.org/10.1038/s41431-022-01280-x
Authors:
Tze Y Lim
Miguel Verbitsky
Simone Sanna-Cherchi
Affiliated Authors:
Tze Y Lim
Miguel Verbitsky
Simone Sanna-Cherchi
Columbia Affiliation:
Subjects:
DNA Copy Number Variations (MeSH)
Genome-Wide Association Study (MeSH)
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Publication Type:
Article
Unique ID:
10.1038/s41431-022-01280-x
PMID:
36631543
DOI:
10.1038/s41431-022-01280-x
Journal:
European Journal of Human Genetics
Publication Date:
Data Source:
PubMed
Source Link:
View PubMed Record

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