A new framework for detecting copy number variants from single nucleotide polymorphism data: 'rCNV', a versatile R package for paralogs and CNVs detection
P. Karunarathne, Q. Zhou, K. Schliep, P. Milesi
The paper introduces rCNV, an R package for detecting copy number variants from SNP data, using statistical methods to analyze allelic-read depth ratios and Hardy-Weinberg equilibrium deviations.
bioRxiv · Oct 14, 2022 · PreprintEvolutionary Biology