Events
enGenome at the AEGH Interdisciplinary Congress on Human Genetics 2026
Spain is one of Europe’s most diverse populations
Spain sits at a unique genetic crossroads.
The Iberian population reflects centuries of migration across North Africa, the Mediterranean, and Northern Europe. The result is a rich and complex genetic landscape, with population-specific variant frequencies that are often underrepresented in global datasets.
As sequencing continues to scale, the bottleneck is no longer data generation. It is accurate, context-aware interpretation.
How can AI-supported interpretation help?
At enGenome, we work with clinical genomics teams to address exactly these challenges.
Our platform enables:
Automated variant prioritisation tailored to phenotype and context
Standardised ACMG-based classification for consistent reporting
Support for complex inheritance models, including digenic and oligogenic cases
AI-assisted literature analysis to accelerate evidence review
Scalable workflows to manage increasing case volumes without increasing team burden
The goal is simple:
Help your team move faster, without compromising accuracy.
Meet the team in Granada
Come and visit us at Booth 30 to discuss your workflows, challenges, and opportunities for automation.
On-site team:
Luisa Cucugliato
Gianluca Passaniti
We’re looking forward to connecting with the Spanish genomics community and learning more about how labs are approaching interpretation at scale.
Book a free live demo
Curious how automated variant interpretation could fit into your workflow?
Book a free personalised demo with our team during the congress
In your session, we will:
Walk through a real clinical interpretation workflow
Show how AI supports variant prioritisation and classification
Discuss how the platform integrates with your existing pipeline
Explore how to reduce turnaround time and increase consistency
About enGenome
enGenome offers innovative solutions for interpreting sequencing data. eVai, the flagship product, is a cloud-based solution fueled by artificial intelligence, that excels in prioritizing genetic variants and has been awarded by the NIH-funded CAGI6 challenge as best performing predictor, elevating diagnostic yield by 12.5%.
The latest release is VarChat, an open-access platform integrating Generative AI that searches and delivers informative text from current scientific literature on genetic variants.
Media Contact: Giovana Herold - marketing@engenome.com
For more information on the conference, access the official website