Events

Leslie Matalonga from the National Center for Genomic Analysis (CNAG), Barcelona will talk about "The Genome-Phenome Analysis Platform (GPAP) - A collaborative platform for diagnosis and gene discovery in rare disease research". Register now!

Florian Buettner from Goethe-University Frankfurt and German Cancer Research Center (DKFZ) will talk about "AI-Driven Analysis of Multi-Omics Data in Personalized Oncology: From Data Integration to Clinical Translation". Register now!

Christian Fufezan from GlaxoSmithKline - Cellzome (Heidelberg) will talk at the GHGA Lecture Series. Register now!

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.

Join the Nextflow community in Barcelona for two days of immersive 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.

This two-day hands-on training in Gatersleben introduces cloud-based research data management. Learn to use de.NBI Cloud resources, manage virtual machines, apply FAIRDOM SEEK, and leverage PLANTdataHUB for collaborative data storage and processing.

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!