FAQs
- Why are some somatic variants not called in the V2 version of the pipeline?
- How do I check why the variant of interest was not called somatic?
- Can I multiplex more than three patients?
- Does the Demultiplexing CSV file need to contain the germline SNV information for all multiplexed samples?
- Is genotype (GT) required for Somatic and Blacklisted variants in the CSV?