For health systems, clinical practices, and academic centers
A modern hereditary cancer risk platform designed to support — not replace — your clinical team.
Continue supportive care after genetic testing
Your patients don't disappear after results. Helix Reserve provides ongoing monitoring, guideline-change alerts, and annual counselor consultations — extending your care without extending your workload.
Decision support for high-risk patients
Structured family history capture and clinical-grade pattern detection helps your team identify which patients warrant referral for genetic counseling or testing.
Guideline-change alerts for your patient panel
When clinical guidelines are updated or new criteria are published, we identify which of your patients are now affected and alert you. No manual re-assessment needed.
Centralized family history capture during intake
Patients complete a guided 15-minute family history intake at home or in your clinic. The structured data integrates with your clinical workflow.
Reduce GC referral overhead through structured triage
Not every patient with a family history concern needs a genetic counselor immediately. Our engine triages patterns so your team can focus on the cases that matter most.
Evidence-based risk methodology
Risk assessment based on family history patterns per established clinical guidelines (Amsterdam II Criteria for Lynch syndrome, Chompret Criteria for Li-Fraumeni, BOADICEA risk model, and others). Genetic testing is one tool among many; family history alone may establish elevated risk warranting surveillance independent of testing outcomes.
How it works
Patient onboarding
Your patients complete a guided family history capture in 15 minutes. Engine produces preliminary pattern analysis.
Clinical review
Your team reviews each case in a familiar pipeline view. Approve, decline, or annotate. Track your patient population over time.
Ongoing monitoring
When clinical guidelines change, we identify which patients in your panel are affected and alert you. No manual re-assessment needed.
Questions
How is this different from existing genetic counseling software?
Modern UX, no tedious data entry, ongoing monitoring built-in. Patients complete family history in 15 minutes, not 45. And the platform actively monitors for guideline changes — it's not a one-shot capture tool.
Is this HIPAA-compliant?
Yes. We operate under BAA agreements with each provider organization. Data is encrypted at rest and in transit on HIPAA-eligible infrastructure.
What does pricing look like?
Pricing is based on patient volume and scope. Contact us for details — we'll build a proposal based on your panel size and clinical workflow.
Can we integrate with our EHR?
EHR integration is on the roadmap. The current product focuses on standalone monitoring with a clean FHIR-compatible export path for family history data.