bioxflow/wgs
In developmentWhole-genome sequencing
Read quality control, trimming, alignment and variant calling for whole-genome sequencing data.
Bioxflow is an open community for developing, reviewing and sharing reproducible analysis pipelines — from raw reads to results.
$ nextflow run bioxflow/rnaseq -profile test,docker
Runs the Bulk RNA-seq pipeline on its bundled test data. About this pipeline →
Pipelines
bioxflow/wgs
In developmentRead quality control, trimming, alignment and variant calling for whole-genome sequencing data.
bioxflow/rnaseq
ReleasedFASTQ to differential expression. Every sample is quantified twice, by Salmon and by STAR, and the two results are compared before DESeq2 runs.
bioxflow/amr
In developmentAssembly and annotation of bacterial genomes with detection of resistance genes, virulence factors and mobile elements.
How it works
Suggest a pipeline and agree on its scope with the community before writing code.
Start from the Bioxflow template: modular processes, containers and a standard layout.
Community review and automated tests check that results are correct and reproducible.
Versioned releases with documentation, test data and citable outputs.
Why Bioxflow
Every step runs in a pinned Docker, Singularity or Conda environment, so results match across machines.
Run the same pipeline on a laptop, an HPC cluster or the cloud by switching one profile.
A shared template, parameter schema and folder structure make every pipeline feel familiar.
Continuous integration runs each pipeline on small test datasets for every change.
Usage guides, parameter references and output explanations come with every release.
Developers, researchers and students design and maintain pipelines together.
Join developers and researchers building the next generation of open, reproducible analysis pipelines.