Events

Join our webinar on GHGA Data Access Request process and learn how to navigate legal roles and master best practices on data access.

Join our webinar to master Nextflow! Learn to build reproducible, cloud-scalable workflows that eliminate pipeline chaos and accelerate your research.

Mark your calendars for 03-05 November 2026 in Heidelberg! GHGA spokespersons, team members, and our Scientific Advisory Board will come together to celebrate achievements, share updates, and plan future work.

This two-day hands-on training in Gatersleben, jointly organized by de.KCD and de.NBI, introduces cloud-based data management and processing. Learn to use de.NBI Cloud resources, FAIRDOM SEEK, Galaxy, and CloWM for life science research.

This five-day Summer School, jointly organized by de.NBI and de.KCD, introduces cloud-enabled genomics, metagenomics, pangenomics, and research data management. Learn to use de.NBI Cloud resources, reproducible workflows, and FAIR practices.

This symposium brings together experts from genomic medicine, research, healthcare, and policy to discuss genomic medicine in Germany. Topics include health data infrastructures, personalized medicine, and insights from the genomDE model project.

The GA4GH 14th Plenary Meeting in Singapore will gather participants from across the health and biomedical ecosystem to advance topics in global genomic and health data sharing.

Join the Nextflow community in Barcelona for two days of learning, hacking, and collaboration. Participate in beginner and advanced Nextflow & nf-core training, and tackle real-world challenges in nf-core hackathon to develop innovative pipelines.

Organised by de.NBI & ELIXIR-DE, the BioHackathon Germany brings together life scientists, bioinformaticians, and data stewards for an intensive week of collaborative hacking - covering FAIR, identifiers, metadata standards, ontologies and metadata catalogues.

Tudor Groza from the Agency for Science, Technology and Research (Singapore) talked about "Towards automating the assembly of natural history of diseases" at the GHGA lecture series. Watch it now!

Unlock the power of Gene Set Enrichment Analysis with R at the GHGA summer school. Dive deep into functional interpretation of omics data. Practical workshops and expert guidance await. Apply now!

Rami Abou Jamra from the University Leipzig talked about "Genome sequencing for rare disease diagnostics: uncovering hidden causal variants" at the GHGA lecture series. Watch it now!

Antje Keppler from EMBL talked about "Euro-BioImaging ERIC - Access to biological and biomedical imaging services" at the GHGA lecture series. Whatch it now!

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.