Enhance healthcare with advanced genomics
eVai platform enables precise and early diagnosis of Rare Disease ensuring unprecedented accuracy in interpreting genomic variants.
eVai platform enables precise and early diagnosis of Rare Disease ensuring unprecedented accuracy in interpreting genomic variants.
AI-powered Suggested Diagnosis
Guideline-based Classification
Continuous Learning
Disease-driven Variant Prioritization
AI-powered Suggested Diagnosis
Guideline-based Classification
Continuous Learning
Disease-driven Variant Prioritization
By combining artificial intelligence with ACMG, AMP and ClinGen guidelines, the award-winning eVai classifies and prioritizes genomic variants by pathogenicity, suggesting the possible genetic diagnoses
Our breakthrough AI technology goes beyond the “one-gene one-disease” paradigm unlocking new diagnoses through the assessment of the pathogenic variant combinations.