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Processing Small Variant Genome VCF
TruSight Tumor 170 small variant genome VCF variants (non-reference calls) with PASS in the Filter column are copied to the Watson for Genomics output VCF. Information from the following columns of the gVCF for the passing variants is included in the output file.
| • | CHROM |
| • | POS |
| • | ID |
| • | REF |
| • | ALT |
| • | QUAL |
| • | FILTER |
| • | INFO |
For Research Use Only. Not for use in diagnostic procedures.