Events

Join our webinar and discover Galaxy's usability boost! New tools like Flexynesis and CELLxGENE simplify multi-omics data exploration and link directly to cloud storage.

Gunnar Rätsch from ETH Zürich will talk about "MetaGraph and its application to collections of human sequencing data". Register now!

Struggling with sensitive human data? Join de.NBI, ELIXIR-DE, and GHGA for hands-on training to secure sensitive human data and ensure GDPR compliance.

Join us for a captivating talk on the critical role of benchmarking and quality control in genomic variant calling.

Join us for The German Model Project Genome Sequencing workshop at the GfH 2025 in Innsbruck! Discover how MV GenomSeq & GHGA are shaping the future of genomic medicine in Germany—bridging healthcare & research to enable groundbreaking secondary research.

Join us for the nf-core hackathon in Heidelberg. GHGA is excited to host the local hub event, bringing together the community for three days of coding, innovation, and tackling all things nf-core.

Thomas Keane from EMBL-EBI talked about "The Federated European Genome-Phenome Archive as a global network for sensitive data discovery and access" at the GHGA lecture series. Watch it now!

Susanna Zucca from enGenome talked about "Using artificial intelligence for the interpretation of genomic variants" at the GHGA lecture series. Watch it now!

GHGA metadata experts Anandhi Iyappan and Karoline Mauer are invited to talk about FAIR data and FAIR portals at the EASE webinar hosted by German Regional Chapter of the European Association of Science Editors. Register for free, if you also love FAIR data!