VarScan is a Java-based, platform-independent software tool that can detect variants in next-generation sequencing (NGS) data. It employs a robust statistical approach to call variants and is able to handle; germline variants, multi-sample variants, somatic mutations and somatic copy number alterations.
Non-Exclusive Agreement Terms
- Field: All uses, including research and commercial applications
- Territory: Worldwide
- Term: 3 years
- Annual License Fee: $10,000 per year
- Annual Use Limit: 1,000 Samples per year
- Sample: means any unique pair of sequence/reference comparison where a sequence of nucleic acids is compared to a reference using Software or Derivative Works of Software. The reference may be a single sequence or collection of sequences.
>> VarScan Non-Exclusive License Agreement (.pdf)
