Unlock the power of Gene Set Enrichment Analysis with R at the GHGA summer school. Dive deep into functional interpretation of omics data. Practical workshops and expert guidance await. Apply now!

Tudor Groza from the Agency for Science, Technology and Research (Singapore) will talk about "Towards automating the assembly of natural history of diseases" at the GHGA lecture series. Register now.

We’re excited to co-organize the genomDE-Symposium 2025! Under the theme "Genomic Medicine. Seizing Opportunities. Helping People.", this event will bring together leading experts from clinics, research, policy, and medical informatics!

Alex Wagner from the Nationwide Children's Hospital, Columbus, USA will talk about "The Variation Representation Specification (VRS) - enabling consistent variant exchange" at the GHGA lecture series. Register now!.

Leslie Matalonga from the National Center for Genomic Analysis (CNAG), Barcelona will talk about "The Genome-Phenome Analysis Platform (GPAP) - A collaborative platform for diagnosis and gene discovery in rare disease research". Register now!

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

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.

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?

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. Watch it now!

Sarah Teichmann from the Wellcome Sanger Institute talked about "(Machine) learnings for the Human Cell Atlas" at the GHGA lecture series. Watch it now!