Skip to content
/ dnaseq Public

Genpipes DNAseq variant calling pipeline implemented in Nextflow

License

Notifications You must be signed in to change notification settings

c3g/dnaseq

Repository files navigation

c3g/dna c3g/dna

GitHub Actions CI Status GitHub Actions Linting Status AWS CI Cite with Zenodo

Nextflow run with conda run with docker run with singularity

Get help on Slack Follow on Twitter Watch on YouTube

Introduction

c3g/dna is a bioinformatics best-practice analysis pipeline for C3G DNAseq pipeline.

The pipeline is built using Nextflow, a workflow tool to run tasks across multiple compute infrastructures in a very portable manner. It uses Docker/Singularity containers making installation trivial and results highly reproducible. The Nextflow DSL2 implementation of this pipeline uses one container per process which makes it much easier to maintain and update software dependencies. Where possible, these processes have been submitted to and installed from nf-core/modules in order to make them available to all nf-core pipelines, and to everyone within the Nextflow community!

Pipeline summary

  1. Read QC (FastQC)
  2. Present QC for raw reads (MultiQC)

Quick Start

  1. Install Nextflow (>=21.10.3)

  2. Install any of Docker, Singularity (you can follow this tutorial), Podman, Shifter or Charliecloud for full pipeline reproducibility (you can use Conda both to install Nextflow itself and also to manage software within pipelines. Please only use it within pipelines as a last resort; see docs).

  3. Download the pipeline and test it on a minimal dataset with a single command:

    nextflow run c3g/dna -profile test,YOURPROFILE --outdir <OUTDIR>

    Note that some form of configuration will be needed so that Nextflow knows how to fetch the required software. This is usually done in the form of a config profile (YOURPROFILE in the example command above). You can chain multiple config profiles in a comma-separated string.

    • The pipeline comes with config profiles called docker, singularity, podman, shifter, charliecloud and conda which instruct the pipeline to use the named tool for software management. For example, -profile test,docker.
    • Please check nf-core/configs to see if a custom config file to run nf-core pipelines already exists for your Institute. If so, you can simply use -profile <institute> in your command. This will enable either docker or singularity and set the appropriate execution settings for your local compute environment.
    • If you are using singularity, please use the nf-core download command to download images first, before running the pipeline. Setting the NXF_SINGULARITY_CACHEDIR or singularity.cacheDir Nextflow options enables you to store and re-use the images from a central location for future pipeline runs.
    • If you are using conda, it is highly recommended to use the NXF_CONDA_CACHEDIR or conda.cacheDir settings to store the environments in a central location for future pipeline runs.
  4. Start running your own analysis!

    nextflow run c3g/dna --input samplesheet.csv --outdir <OUTDIR> --genome GRCh37 -profile <docker/singularity/podman/shifter/charliecloud/conda/institute>

Documentation

The c3g/dna pipeline comes with documentation about the pipeline usage, and output.

Credits

The Genpipes DNAseq pipeline was originally written by Mathieu Bourgey, Rob Eveligh, and Edouard Henrion and translated into the c3g/dna Nextflow workflow by Rob Syme,

Contributions and Support

If you would like to contribute to this pipeline, please see the contributing guidelines.

Citations

An extensive list of references for the tools used by the pipeline can be found in the CITATIONS.md file.

The pipeline structure is a translation of the Genpipes DNAseq pipeline.

GenPipes: an open-source framework for distributed and scalable genomic analyses

Mathieu Bourgey, Rola Dali, Robert Eveleigh, Kuang Chung Chen, Louis Letourneau, Joel Fillon, Marc Michaud, Maxime Caron, Johanna Sandoval, Francois Lefebvre, Gary Leveque, Eloi Mercier, David Bujold, Pascale Marquis, Patrick Tran Van, David Morais, Julien Tremblay, Xiaojian Shao, Edouard Henrion, Emmanuel Gonzalez, Pierre-Olivier Quirion, Bryan Caron, Guillaume Bourque

GigaScience 2019 June. doi: 10.1093/gigascience/giz037.

This pipeline uses code and infrastructure developed and maintained by the nf-core community, reused here under the MIT license.

You can cite the nf-core publication as follows:

The nf-core framework for community-curated bioinformatics pipelines.

Philip Ewels, Alexander Peltzer, Sven Fillinger, Harshil Patel, Johannes Alneberg, Andreas Wilm, Maxime Ulysse Garcia, Paolo Di Tommaso & Sven Nahnsen.

Nat Biotechnol. 2020 Feb 13. doi: 10.1038/s41587-020-0439-x.

About

Genpipes DNAseq variant calling pipeline implemented in Nextflow

Resources

License

Code of conduct

Stars

Watchers

Forks

Releases

No releases published

Packages

No packages published