The First Version of HandyCNV
What's New
The first version of HandyCNV.
Range of application
Post-analysis of CNV and ROH detected from SNP genotyping data. Each function does not limit the number of chromosomes, theoretically applicable to most diploid organisms. So far, it has been successfully tested in sample of 2,000 Bovine 150K SNP chip.
Main feature
An one-stop analysis that integrates the summary, annotation, conversion, comparison and visualization, the custom input arguments and verbose outputs will help the users to identify the most interesting genome regions.