What’s Happening at enGenome

enGenome and Genetic Alliance Partner to Expand Access to Advanced Genomic Interpretation for Rare Disease

Collaboration, initiated through Genetic Alliance laboratory partner, Dubai H…

enGenome celebrates 10 years of innovation in genomic variant interpretation

The company celebrates ten years of activity and growth as an international p…

VarChat now available in MobiDetails for faster literature access

With this integration, users can quickly find scientific literature on genomi…

VarChat integrated on the UCSC Genome Browser!

Integration allows users to quickly access literature on genomic variants dir…

Run for Rare 2025: Let’s make every step count!

enGenome takes a step towards raising awareness for rare diseases by organizi…

New VarChat Chatbot: interactive conversations for better insights

enGenome’s Run for Rare to raise awareness for Rare Disease Day

enGenome took a step towards raising awareness for rare diseases by organizin…

enGenome launches VarChat: the first GenAI genomic variant assistant

enGenome announces today the release of VarChat: an open platform designed to…

“We Care About Rare”: enGenome’s new campaign on Rare Disease

enGenome’s eVai platform is a best performer in the NIH-funded CAGI6 Challenge

Rare Disease Day 2022: Marfan Syndrome

enGenome among start-up champions to receive funding from European Innovation Council Accelerator