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URL: https://github.com/abyzovlab/CNVpytor
Proper Citation: CNVpytor (RRID:SCR_021627)
Description: Software Python package and command line tool for CNV/CNA analysis from depth of coverage by mapped reads. Software tool for CNV/CNA detection and analysis from read depth and allele imbalance in whole genome sequencing.
Resource Type: software application, sequence analysis software, data analysis software, data processing software, software resource
Defining Citation: DOI:10.1101/2021.01.27.428472
Keywords: Copy number variations, copy number alternations, whole genome sequencing, Python
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