A tool for visualizing copy number variation (CNV) and single nucleotide polymorphism (SNP) data. VCS can visualize the enrichment of genome contents in CNV, CNV and/or SNP physical distribution, the log 2 CNV distribution ratio, the number of CNVs and SNPs per binning, homozygosity distribution of genotypes, and a cytomap of genes.
Genetic variation
Kim H, Sung S, Cho S, Kim TH, Seo K, Kim H "VCS: Tool for Visualizing Copy Number Variation and Single Nucleotide Polymorphism." Asian-Australas J Anim Sci. 2014 Dec;27(12):1691-4. https://doi.org/10.5713/ajas.2014.14143
PMID: 25358361
PMCID: PMC4213679
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