Enhance healthcare with advanced genomics
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
Monogenic and digenic interpretation
AI-powered Suggested Diagnosis
Guideline-based Classification
Continuous Learning
Monogenic and digenic interpretation
By combining AI with international guidelines, our award winning technology classifies and prioritizes genomic variants by pathogenicity, suggesting the possible genetic diagnoses.
VarChat is the first open platform to use Generative AI for searching genomic variants in literature and synthesizing information in a coherent and concise way.
Some of our happy clients
Since 2011 our scientific team has been developing different bioinformatics workflows (DNA-Seq, RNA-Seq, Liquid Biopsy) for customers worldwide.
Latest news
View more 
Webinar
ESHG Sneak peek: Finding order in genomic disorders with enGenome’s AI
15 April 2024
Events
enGenome invited to talk on AI to advance variant interpretation at HUGO 2024
28 March 2024
News
enGenome’s Run for Rare to raise awareness for Rare Disease Day
29 February 2024