The NF-PCGR (Nextflow-based Pipeline for Clinical Genome Reports) is an open-source pipeline for generating clinical genome reports using the PCGR framework. During this hackathon, we aim to update the functionality of NF-PCGR and try to complete the integration with sarek.

Goal

By the end of the hackathon, we aim to achieve the following:

  • Integrate new variant annotation sources to improve reporting.
  • Optimize pipeline execution for better performance.
  • Start the integration with nf-core sarek

How to Get Involved

If you’re interested in contributing, check out the NF-PCGR repository for existing issues and ideas. Feel free to join our Slack discussions and submit pull requests!


Let’s collaborate to improve NF-PCGR and make it a powerful tool for clinical genomics!