This Data Protection Course is designed for anyone who works with personal data in the biomedical field, including healthcare professionals, researchers, administrators, and data stewards.

The upcoming conference on "Functional Epigenomics", organised by GHGA member Jörn Walter, features an outstanding line-up of speakers, including GHGA members Oliver Stegle, Joachim Schultze and Philip Rosenstiel. Registration is now open!

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?

Steven Laurie from the Spanish National Centre for Genomic Analysis (CNAG) will talk about "The RD-Connect Genome-Phenome Analysis Platform (GPAP)" at the GHGA lecture series. Register now!

Sarah Teichmann from the Wellcome Trust Sanger Institute will talk about "(Machine) learnings for the Human Cell Atlas" at the GHGA lecture series. Register now!

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.

Ascona2024 is a one week workshop on statistical modelling of spatial and temporal omics data

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.

New to single cell research? Looking for an introduction into scRNA sequencing and analysis workflows? Then look no more, we have a webinar for you.

Marina DiStefano (Broad Institute) will present "The Gene Curation Coalition: A Global Effort to Harmonize Gene-Disease Evidence Resources". Watch it now!