A new framework for detecting copy number variants from single nucleotide polymorphism data: ‘rCNV’, a versatile R package for paralogs and CNVs detection

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Karunarathne P, Zhou Q, Schliep K, Milesi P

- - (-) - [2022-10-18; online 2022-10-18]

DOI 10.1101/2022.10.14.512217

Crossref 10.1101/2022.10.14.512217