Variant Interpretation Services

Variant Interpretation Services

Evidence-based variant associations with genotype-phenotype correlations including molecular function, diagnostic, prognostic, and therapeutic relevance, available treatments, and open clinical trials

Variant Interpretation
  • Clinical relevance of a gene variant, with supporting evidence from trials, Guidelines, and approval documents
  • Profiling of Somatic and Germline variants associated with Pathogenicity, Oncogenicity, Druggability and Treatment response
Biomarker Knowledge & Discovery
  • Biomarkers and their uses across the full spectrum of drug discovery and development, risk, protection, diagnosis, prognosis, efficacy, safety and resistance
  • Clinical and preclinical qualification of the biomarkers along with their correlation to the endpoints.