Events

Join our webinar and discover Galaxy's usability boost! New tools like Flexynesis and CELLxGENE simplify multi-omics data exploration and link directly to cloud storage.

Gunnar Rätsch from ETH Zürich will talk about "MetaGraph and its application to collections of human sequencing data". Register now!

Struggling with sensitive human data? Join de.NBI, ELIXIR-DE, and GHGA for hands-on training to secure sensitive human data and ensure GDPR compliance.

Alex Wagner from the Nationwide Children's Hospital, Columbus, USA talked about "The Variation Representation Specification (VRS) - enabling consistent variant exchange" at the GHGA lecture series. Watch it now!

We’re excited to co-organize the genomDE-Symposium 2025! Under the theme "Genomic Medicine. Seizing Opportunities. Helping People.", this event will bring together leading experts from clinics, research, policy, and medical informatics!

Tudor Groza from the Agency for Science, Technology and Research (Singapore) talked about "Towards automating the assembly of natural history of diseases" at the GHGA lecture series. Watch it now!

Unlock the power of Gene Set Enrichment Analysis with R at the GHGA summer school. Dive deep into functional interpretation of omics data. Practical workshops and expert guidance await. Apply now!

Rami Abou Jamra from the University Leipzig talked about "Genome sequencing for rare disease diagnostics: uncovering hidden causal variants" at the GHGA lecture series. Watch it now!

Antje Keppler from EMBL talked about "Euro-BioImaging ERIC - Access to biological and biomedical imaging services" at the GHGA lecture series. Whatch it now!