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.

New to the field of epigenetics and its analysis methods? Or just looking for a brief intro to the topic? Then we have a webinar for you - in ‘A Beginners Guide to Epigenetics’ we will talk about the basics of epigenetic research and analysis methods.

Struggling with interpreting statistical results? Join our next webinar on Interpretation of Results from Biostatistics.

Peter Robinson from The Jackson Laboratory (JAX), presented "The Phenopacket schema: an open standard for sharing disease and phenotype information". Watch it now!

GHGA is going to participate at the GfH conference (German Society for Human Genetics) and will organize a workshop titled “The German Human Genome-Phenome Archive (GHGA): Best practice examples for shared genome data usage”.

Christoph Schickhardt from the National Center for Tumor Diseases Heidelberg (NTC) will talk about "A standardized broad consent for long-term secondary use of health data and biosamples". Watch it now!

Have heard of Galaxy - the open source, web-based platform for data intensive biomedical research? Tune in to our webinar to learn what it does, which tools it provides and how it can help your research!