CNVkit is a tool for detection and visualization of copy number variation (CNV). The algorithm uses targeted and off-target sequence reads for the inference of CNV.
DNA structural variation
Talevich E, Shain AH, Botton T, Bastian BC "CNVkit: Genome-Wide Copy Number Detection and Visualization from Targeted DNA Sequencing." PLoS Comput Biol. 2016 Apr 21;12(4):e1004873. https://doi.org/10.1371/journal.pcbi.1004873
PMID: 27100738
PMCID: PMC4839673
If you find errors, please report here.
SECTIONS
TutorialsFind thousands of Bioinformatics and Life Science software tools and databases in the newly launched
Ads