Pathogenic variants ranked in first positions
Classification accuracy up to 98%
VUS reduction up to 60%
Intuitive and Fast
Secure and CE IVD marked
The eVai platform automates ACMG guidelines and prioritizes variants to highlight candidate diagnoses.
Pathogenic variants ranked in first positions
Classification accuracy up to 98%
VUS reduction up to 60%
Intuitive and Fast
Secure and CE IVD marked
eVai automatically pre-classifies SNV, Indels and CNVs according to international guidelines. The classification is disease-specific and reports both the activated criteria and the supporting evidence.
eVai leverages our proprietary AI technology to assign a pathogenicity score to each variant thus enabling their prioritization. Even VUS get a score and can be therefore stratified.
Variant-disease associations can be submitted to a private lab repository that can contribute to significantly improve classification and prioritization performances over time. Moreover, the lab repository can be used to store info about variant artifacts.
By integrating more than 30 omics resources, eVai is constantly up-to-date with the current genomic literature, from population databases (e.g. gnomAD) to gene-disease ones (e.g. MedGen).
Analyze trio, quartet or up to 7 family members: for each variant, eVai will automatically infer the possible inheritance patterns according to a fully penetrant disease. Users can select the variants that fit certain inheritance patterns and quickly compare genotypes across the members.
eVai enables users to create virtual gene panels and custom variant filters by leveraging on multiple omics resources such as Human Phenotype Ontology.
Make your interpretation process intuitive, faster and more accurate.
Our breakthrough AI technology goes beyond the “one-gene one-disease” paradigm unlocking new diagnoses through the assessment of the pathogenic variant combinations.