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.

Guests are welcome! GHGA will hold a public symposium on 15 October 2024 in Heidelberg, as part of the GHGA Annual Meeting 2024.

We are pleased to announce that registration for the GHGA Annual Meeting 2024 is now open.

Join us to discover how a large Nanopore Long-Read Genome Sequencing (LR-GS) dataset can revolutionise rare diseases diagnostics

We are excited to announce that GHGA will be presenting a tutorial on NGS Workflow Harmonization at the upcoming German Conference for Bioinformatics on September 30, 2024.

Why are metadata important for research and data analysis? Which genomic data portals are out there and what do we need from them? How do we make our research data FAIR?

Zornitza Stark and Sebastian Lunke from the Victorian Clinical Genetics Services will talk about "Integrated multi-omics for rapid rare disease diagnosis on a national scale" at the GHGA lecture series. Watch it now!