Welcome to myVCF manual page!
myVCF is a user-friendly platform that helps end-users, without programming skills, to analyze and visualize mutations in an easy and flexible manner. Helping decision making for further downstream analysis.
myVCF will manage VCF (Variant Call Format) files (the standard format for storing NGS mutations data) deriving from different NGS applications (Whole Exome/Genome sequencing, Public database...)
myVCF will help end-users to browse and analyze VCF coming from exome and targeted sequencing projects. myVCF can handle multiple-sample VCF and multiple projects can be created as separate environment in order to manage different VCFs with the same application.
Want to try myVCF?¶
You can download myVCF package from:
and follow the instructions contained in the installation page
- 1. Install the package
- 2. Setup a project
- 3. myVCF features
- 4. FAQ
How to cite myVCF¶
Paper under review!!
Update will be available soon. Fingers crossed :)