Events

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

  Partner Events     Past Events

GHGA Events

The de.NBI & ELIXIR-DE and GHGA Knowledge Series: Enhancing Gene Ontology for Medical Lipidomics

Unlock functional insights with MAPtoGO: Join our webinar to master simultaneous GO-based enrichment across lipidomics, proteomics, and multiomics datasets.

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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.

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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.

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GHGA Annual Meeting 2026

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.

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Partner Events

No news available.

Past GHGA Events

GHGA Annual Meeting 2024

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

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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

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GHGA Workshop on NGS Workflow Harmonization at the German Conference for Bioinformatics 2024

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.

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Webinar: FAIR biomedical data for FAIR portals

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?

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GHGA Lecture Series: Zornitza Stark and Sebastian Lunke (virtual)

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!

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