The variant call format (VCF) is a popular file format for human genome variation data. Tools have been developed to perform analyses of VCF data such as population genetics and variant prediction. However, tools required for other genetic analyses are lacking for the VCF format. VCFDataPy is a software tool that can perform various analyses such as Identity by State, Inheritance patterns in trios and Copy Number Variation on human genome.

Authors:

Siddharth Krishnakumar (Presenter)
TJHSST

Jonathan Pevsner, Kennedy Kreiger Institute