Tertiary Pipelines¶
Tertiary pipelines take a VCF — usually produced upstream by a secondary pipeline — and produce annotated, classified, report-ready variants. Each clinical reporter is its own tertiary pipeline.
Inputs¶
- VCF — the output of a secondary run (or an externally-provided VCF that meets the requirements).
- Sample metadata — tumor type, suspected phenotype, family history, depending on the reporter.
- Common inputs shared across reporters — see Common Inputs.
Outputs¶
- Annotated VCF with per-variant pathogenicity, ACMG criteria (for hereditary) or AMP/ASCO/CAP tier (for somatic), gene-level annotations, population frequencies.
- A report-ready dataset that the Report entity can render into a clinical PDF.
Reporters available¶
- GS Hereditary Reporter
- GS Hereditary Cancer Reporter
- GS Somatic Reporter
- GS Myeloid Reporter
- GS PGX Reporter
See also¶
- Common Inputs — reference genome, BED files, gene panels.
- Requirements — minimum metadata and QC thresholds.
- Variant Filtering — how the outputs surface in the UI.