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.

GHGA is going to participate at the GfH conference (German Society for Human Genetics) and will organize a workshop titled “The German Human Genome-Phenome Archive (GHGA): Best practice examples for shared genome data usage”.

Christoph Schickhardt from the National Center for Tumor Diseases Heidelberg (NTC) will talk about "A standardized broad consent for long-term secondary use of health data and biosamples". Watch it now!

Have heard of Galaxy - the open source, web-based platform for data intensive biomedical research? Tune in to our webinar to learn what it does, which tools it provides and how it can help your research!

In this webinar we will give you an introduction to what it takes to make data in this field Findable, Accessible, Interoperable and Reproducible - and how the FAIR principles can be implemented.

New to single cell research? Looking for an introduction into scRNA sequencing and analysis workflows? Then look no more, we have a webinar for you.

Marina DiStefano (Broad Institute) will present "The Gene Curation Coalition: A Global Effort to Harmonize Gene-Disease Evidence Resources". Watch it now!