Provides insights into how sharing human omics data can revolutionise research and health care.
Discusses personal genome sequencing and its benefits for rare disease and cancer research (Working Group Gene Technology Report, in cooperation with GHGA)-
The national infrastructure for secure and FAIR sharing of human omics data.
Facilitating streamlined discovery of and access to human omics data.
Harmonising the way human omics data is described in different settings with the GHGA Metadata Mode
GHGA's multi-layered approach to protect sensitive human omics data
Tools to help clinicians, researchers and institutions wanting to submit omics data to GHGA
Standardised, comparable, and reproducible omics workflows for the research community
Engaging with research and clinical communities via outreach and training activities
Bringing genomic medicine into standard care while making human omics data available for research via GHGA.
Strengthening Germany's and Europe’s Bioinformatics Infrastructure.
