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Conversion to Watson for Genomics VCF
The TruSight Tumor 170 + Watson for Genomics Converter app processes the DNA small variant genome VCF and the RNA splice variant VCF from the TruSight Tumor 170 app to generate a combined VCF output that includes DNA small variants and RNA splice variants.
NOTE
When analyzing DNA app results only, the input is the small variant genome VCF.
When analyzing RNA app results only, the input is the splice variant VCF.
When no passing variants exist in the input file(s), the TruSight Tumor 170 + Watson for Genomics Converter app does not create a VCF output. This is captured in the Summary Report.
For Research Use Only. Not for use in diagnostic procedures.