End of April, the GHGA development team participated in the "ELIXIR Compute Platform 2022 Face-to-Face Meeting" in Berlin and introduced the GHGA mission and architecture strategy to the Compute Platform members.
The NGS community came together to highlight the role of sequencing in crisis and establish a clear picture for the future of sequencing across all areas of life science.
Inversions in the human genome form more commonly than previously thought, impacting our understanding of genetic stability and diseases.
How does genome research actually work and how do you figure out which letters (of the DNA bases) lead to which body function? Find out more in this new podcast episode! (The podcast is only available in German.)
A new study introduces a workflow with the clinical implementation of RNA sequencing in conjunction with DNA sequencing to diagnose patients with rare genetic disorders.
Within a participatory study, GHGA will hold deliberative democratic forums exploring the patients’ perspectives and which concrete roles patients could take within GHGA governance.
The moon landing of genetic research, i.e. the first full sequence of the human genome, was a milestone in genetic research. Find out more about the research, techniques and the people involved in this new podcast episode! (The podcast is only available in German.)
With our goal in mind to create and implement best-practise workflows, GHGA team members attended the nf-core hackathon.
GHGA participated at the GfH conference (German Society for Human Genetics) and organized a workshop titled “The German Human Genome-Phenome Archive (GHGA): Best practice examples for shared genome data usage”.
As part of the IdeenLauf all citizens are invited to put their questions to science forward. As a consortium of the NFDI e.V., GHGA is particularly involved in the area of research data management.
The new GHGA podcast starts on March 1, 2022!
