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.
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First GHGA webinar was successfully held - it included a Beginners Guide to DNA and Sequencing and an introduction to bioinformatic workflows.
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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.
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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.
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With our goal in mind to create and implement best-practise workflows, GHGA team members attended the nf-core hackathon.
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