Integrated, case-centric, evidence-backed, lightning-fast analysis.
Active case
Patient 042 · Pediatric tumor
DNA variants
SNV · Indel
Structural
SV · STR
Tumor omics
RNA · Fusion · Methylation
Prioritized evidence
Signals that converge on the case
Phenotype
Matched
Clinical
Pathogenic
Tumor
Supported
One connected workflow
FlashVCF is built for the questions that no single assay can answer alone.
Capture phenotype, family structure, tumor diagnosis, samples, and collaborators before analysis begins.
Analyze small variants, structural variants, STRs, RNA expression, fusions, and methylation in the same case workspace.
Layer phenotype, inheritance, population frequency, clinical knowledge, functional prediction, and tumor-specific associations.
Use focused filters, gene, disease and panel views, bookmarks, notes, and case-level sharing to keep review moving.
Built for converging evidence
Bring the analyses available for your patient or tumor into one place, then let the evidence guide the next question.