Baseshift transforms VCF files, phenotypes, panels, cohorts, and longitudinal biomedical data into decision-ready research intelligence — with explainability, validation, and AI reasoning built in.
Progress, panels, scoring, PDF.
Explain variants, compare samples, prioritize findings.
Evidence-aware interpretation.
Filter findings by ACMG, hereditary cancer, cardiac, pharmacogenomics, and custom lab panels.
02 · CompareSee shared and unique variants, inheritance patterns, and cohort-level signal.
03 · TrustExpose why each finding was prioritized with evidence, confidence, and actionability.
A customer-ready demonstration of pathogenic findings, evidence review, AI interpretation, and clinical-style reporting.