Join our new NGS Pipeline Benchmarking efforts

Benchmarking small pathogenic and structural variants can be challenging. Utilizing cutting-edge SeraSeq, GHGA partners with the NGS-CN to start a new initiative to benchmark NGS pipelines.

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GHGA at the de.NBI/ELIXIR-Germany Spatial Hackathon

GHGA joined the de.NBI/ELIXIR-Germany Spatial Hackathon ‘SpaceHack2.0’, advancing community-driven benchmarking.

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Benchmarking genomic variant calling

A recent publication, spearheaded by the Next Generation Sequencing Competence Network (NGS-CN) and GHGA, introduces NCBench, a platform for continuous benchmarking of genomic variant calling workflows.

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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.

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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.

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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.

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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.

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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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