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.

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

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.

Unlock the power of NGS harmonization! Join us for a two-part virtual webinar series on workflow standardization and benchmarking, featuring practical tips and best practices for achieving harmonization using the Sarek pipeline as an example.

This course is designed to provide an overview of data protection regulations and obligations, with a focus on the General Data Protection Regulation (GDPR).

Martin Hirst from the University of British Columbia (UBC) talked about "THe EpiATLAS – a reference for human epigenomic research". Watch it now!

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!