Vgen23 supports germline and somatic interpretation workflows across multiple test types, variant classes, and sequencer outputs.
Review single-patient exomes and panels with phenotype-to-genotype and genotype-to-phenotype support in one workflow. Aggregate evidence, inspect candidate variants, and move selected findings into a report-ready draft.
Support family-based review with de novo and segregation analysis, including workflows that help teams inspect inheritance patterns and prioritize findings faster.
Run structured interpretation workflows for disease-focused panels without switching tools or rebuilding report logic each time.
Support somatic interpretation with tumor-focused workflows that bring evidence review and structured reporting into the same environment.
Upload a solved or unsolved case and see how Vgen23 fits into your current interpretation process.
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