Genovar is a tool for detection of copy number variation (CNV). It can compare detected CNVs with variants in the Database of Genomic Variants ( DGV) to find out whether variants are novel or previously detected. Genovar can visualize genomic source data, e.g., aCGH and sequence alignment data.
Genetics; DNA mutation; Data visualisation; DNA; Sequence analysis
Jung KS, Moon S, Kim YJ, Kim BJ, Park K "Genovar: a detection and visualization tool for genomic variants." BMC Bioinformatics. 2012 May 8;13 Suppl 7:S12. https://doi.org/10.1186/1471-2105-13-S7-S12
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