Variant Interpretation Services
Maven’s Variant Interpretation Services provide evidence-based associations between gene variants and genotype-phenotype correlations. These include molecular function, diagnostic and prognostic relevance, therapeutic importance, existing therapies, and open clinical studies.
Clinical Significance of Variants
We assess the clinical impact of somatic and germline variations based on trials, guidelines, and regulatory approvals. Our analysis includes:
- Pathogenicity
- Oncogenicity
- Drugability
- Treatment response
Biomarker Research & Development
We support biomarker discovery and qualification for use in drug development and clinical practice. Applications include:
- Risk and protection profiling
- Diagnostic and prognostic markers
- Efficacy and safety indicators
- Resistance mechanisms
Our services span both preclinical and clinical biomarker qualification and their linkage to study endpoints.
