how it works
Re-Solve turns genetic uncertainty
into Clinical Certainty
The first expert curation platform to unlock the clinical value of VUS.
1
Clinical Ingestion & Standardization
We securely onboard genetic variants from any certified laboratory report. Our engine performs immediate Quality Assurance and Nomenclature Verification (HGVS/ACMG standards), transforming static lab results into standardized, high-fidelity digital assets ready for active monitoring.
2
Dynamic Monitoring & Evidence Tracking
Variants of Uncertain Significance (VUS) are securely monitored against the global evolution of genomic science. Our engine continuously cross-references your data with the latest clinical evidence.
3
Resolve
Every six months, you receive from our experts a Genetic Re-Solution Report. Even if no changes occur, we confirm the ongoing monitoring of your data. If a variant is reclassified, we provide an immediate actionable update and a direct bridge to the necessary clinical pathways.
4
Counselling -Expert Guidance When it Matters
You are never left alone with your data. If our monitoring identifies a clinically significant re-classification, we immediately provide a dedicated Genetic Counseling session. Our specialists will guide you and your physician through the new findings, ensuring every Genetic Re-Solution is translated into a clear, actionable medical path.
Who Resolve can Assist
Uncertainty is a common problem,
Resolution is possible
We help to transform uncertain results into clear, actionable guidance
through personalized solutions.
Patients
Discovery the opportunities to reinterpret your inconclusive genetic testing results
Physicians
Receive guidance on patient care from clear genetic results.
Laboratories
Enhance lab performance through clear and actionable genetic data.
Partners
Drive innovation. Improve patient outcomes.