OpenCRAVAT · variant annotation
Annotates and prioritises genomic variants using selectable modules for investigating cancer genomes.
Conditions of use
Provide a variant or VCF with the reference genome and appropriate annotators; record module versions and the sample’s origin.
Limits and context
Automatic annotation does not determine pathogenicity or therapeutic action; evidence and clinical classification require specialist review. The modules were not run.
Catalogued source record. Implementation on ELUCENIA and independent scientific review pending.
Relationship with cancer research
Support for research — context required
The project documentation and NCI catalogue describe modular variant annotation.
Applications: Genomics · Biomarkers