Major bioinformatic workflow releases with GHGA contribution

The GHGA workflow workstream was involved in the release of bioinformatic workflows (sarek 3.0, nanoseq 3.0, and DROP 1.2), collaborating with the nf-core community and the Gagneur lab.

GHGA Training Webinar Series started

First GHGA webinar was successfully held - it included a Beginners Guide to DNA and Sequencing and an introduction to bioinformatic workflows.

GHGA represented at ELIXIR Compute Platform Meeting

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.

Clinical implementation of RNA sequencing in rare genetic disorders

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.

GHGA attends nf-core hackathon

With our goal in mind to create and implement best-practise workflows, GHGA team members attended the nf-core hackathon.

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