cancelled! Join us for a captivating talk on the critical role of benchmarking and quality control in genomic variant calling.

Kyle Farh from Illumina will talk about "How do you train genomics AI?" at the GHGA lecture series. Register now!

Curious about Research Data Management (RDM) and its significance, especially in human research? de.NBI and GHGA have designed the ideal interactive training session for you, combining informative presentations with hands-on exercises!

Join the nf-core Hackathon to connect with fellow Nextflow and nf-core enthusiasts! Dive into three days of collaboration, coding, and innovation, tackling everything nf-core.

The 11th ELIXIR All Hands Meeting will bring together members of the community from across the ELIXIR nodes and collaborators from partner organisations to review ELIXIR's recent achievements and activities, and to discuss future plans.

Save the date for the second Conference on Research Data Infrastructure in Aachen! Explore how better use of research data drives knowledge and benefits society, with keynotes, lectures, posters, and a market of opportunities.

GA4GH 13th Plenary Meeting in Uppsala will bring together the global genomics and health community for workshops, presentations, and keynote talks that explore opportunities to scale genomic and clinical data sharing.

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!