Events

On this page we share the latest Events, both posted by us and our Partners.

  Partner Events     Past Events

GHGA Events

nf-core hackathon: local hub event Heidelberg 2026

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.

Learn more

The de.NBI & ELIXIR-DE and GHGA Knowledge Series: Reproducible and Scalable Workflows with Nextflow

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

Learn more

The de.NBI & ELIXIR-DE and GHGA Knowledge Series: GHGA Data Access: A Guide to Legal Roles and Rules

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

Learn more

Partner Events

No news available.

Past GHGA Events

GHGA at the DKFZ Open Day

Join us at when the DKFZ opens its doors to the public for a debate on the use of genomic data for research. This lively format will give everyone the chance to explore data sharing from impact to data protection.

Learn more

GHGA Webinar: Understanding Genetic Discrimination

Discover the hidden history of genetic discrimination. Join us to learn about the implications for research and policy, and how we can work towards a more equitable future.

Learn more

GHGA Lecture Series: Anthony Brookes (virtual)

Anthony Brookes from the University of Leicester talked about "Research Asset Discovery in Large European Networks" at the GHGA lecture series. Watch it now!

Learn more

GHGA Symposium 2024

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

Learn more

GHGA Annual Meeting 2024

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

Learn more

GHGA Webinar: Rare Disease Diagnostics in Complex Genomic Regions with Long Reads

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

Learn more