Join us at when the DKFZ opens its doors to the public for a debate on the use of genomic data for research. This lively format will give everyone the chance to explore data sharing from impact to data protection.

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

Enabling closer collaboration, we are pleased to announce the first NFDI BioMed Workshop in Heidelberg bringing together NFDI4Bioimage, NFDI4Health, NFDI4Immuno, NFDI4Microbiota and GHGA.

Gerrit Meijer from the Netherlands Cancer Institute will talk at the GHGA lecture series. Register now!

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

Join Base4NFDI’s first User Conference, showcasing new RDM services for the NFDI community. This two-day event will present key services, explore integration options, and address interoperability with national and European infrastructures.

The 10th e:Med Meeting on Systems Medicine in Hamburg will bring together members and other interested scientists. The topics of this year's meeting are technologies, modelling and bioinformatics approaches, diseases and systems medicine approaches in the clinic.

This year’s user meeting focuses on experienced users. The online event will feature advanced workshops on container orchestration with Kubernetes and managing cloud-based clusters, fostering collaboration and addressing community needs.

Get to know the currently funded Base4NFDI basic services! This online event features short presentations from each service team on goals and current developments, followed by open discussions. Open to all – NFDI-wide and everyone interested.

The workshop covers bioinformatic processing of DNA methylation data, focusing on methylation arrays. It includes quality checks, normalization, differential analysis, and advanced deconvolution methods. Organized by GHGA member Jörn Walter.

de.NBI and ELIXIR Germany host the 3rd BioHackathon in Kassel, focused on advancing open-source infrastructure in bioinformatics - covering FAIR data, metadata standards, secure cloud environments, and training tools.

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!

In this webinar we will give you an introduction to what it takes to make data in this field Findable, Accessible, Interoperable and Reproducible - and how the FAIR principles can be implemented.