Interpret · OnKommon Interpreter
Genomic interpretation
- What happens
- The tumour genome is sequenced by whole-exome sequencing. Variants are catalogued, filtered and annotated, and each alteration is weighed against curated evidence.
- Inputs
- Solid-tumour whole-exome sequencing data and relevant clinical context.
- Intended output
- A structured molecular interpretation: drivers, response biomarkers, supporting evidence and the findings to watch.
- What it establishes
- Which alterations drive this tumour, and how strong the evidence is for each.
- Why it matters
- It tells AVATAR which drivers to carry into the living model.

