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nf-core/pairgenomealign

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Pairwise genome comparison pipeline using the LAST software to align a list of query genomes to a target genome, and plot the results

Is nf-core/pairgenomealign beginner-friendly?

We have not seen enough recent pull requests from outside contributors to nf-core/pairgenomealign to say how often they are merged. 2 beginner-friendly issues are open now.

Stars
11
Forks
6
Open beginner issues
2
Indexed issues
18
Avg merge
7h 49m
Merged PRs (30d)
4
Dominant language
Nextflow
License
MIT
Last GitHub push
Oct 8, 2026
Latest indexed
Sep 19, 2026
Contributing guide
Code of conduct
Beginner labels
No beginner labels indexed

How to contribute to nf-core/pairgenomealign

  1. Read the contributing guide first: it says how the maintainers want changes proposed, tested and reviewed.
  2. The project ships a dev container: open it in Codespaces to get a working environment in your browser.
  3. Read its code of conduct: it covers issues and pull requests as well as chat.
  4. Pick one of the 2 open beginner-friendly issues below and comment that you want to work on it before you start.
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