Join us to discover how a large Nanopore Long-Read Genome Sequencing (LR-GS) dataset can revolutionise rare diseases diagnostics

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.

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!