Zornitza Stark and Sebastian Lunke from the Victorian Clinical Genetics Services will talk about "Integrated multi-omics for rapid rare disease diagnosis on a national scale" at the GHGA lecture series. Register now!

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?

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.

We are pleased to announce that registration for the GHGA Annual Meeting 2024 is now open.

Guests are welcome! GHGA will hold a public symposium on 15 October 2024 in Heidelberg, as part of the GHGA Annual Meeting 2024.

Anthony Brookes from the University of Leicester will talk about "Research Asset Discovery in Large European Networks" at the GHGA lecture series. Register now!

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!

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.

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!