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
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News
New VarChat Chatbot: interactive conversations for better insights
4 November 2024
Events
enGenome to showcase new breakthrough VarChat feature at ASHG 2024 in Denver
28 October 2024
Events
enGenome in Palermo for insights on AI in variant interpretation
8 October 2024