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Pipeline that runs bcl2fastq and creates additional plots within a Snakemake workflow

Project description

This is is the demultiplex pipeline from the Sequana projet

Overview:Runs bcl2fastq on raw BCL data and create some QC plots to ease the QC step
Input:A valid Illumina base calling directory
Output:a set of PNG files and the expected FastQ files
Citation:Cokelaer et al, (2017), ‘Sequana’: a Set of Snakemake NGS pipelines, Journal of Open Source Software, 2(16), 352, JOSS DOI https://doi:10.21105/joss.00352


You must install Sequana first:

pip install sequana

Then, just install this package:

pip install sequana_demultiplex


sequana_pipelines_demultiplex --help
sequana_pipelines_demultiplex --input-directory DATAPATH --run-mode local
sequana_pipelines_demutliplex --input-directory DATAPATH --run-mode slurm

This creates a directory fastq. You just need to execute the pipeline:

cd demutliplex
sh  # for a local run

This launch a snakemake pipeline. If you are familiar with snakemake, you can retrieve the demutliplex.rules and config.yaml files and then execute the pipeline yourself with specific parameters:

snakemake -s demutliplex.rules --cores 4 --stats stats.txt

Or use sequanix interface.


This pipelines requires the following executable(s):

  • bcl2fastq 2.20.0


This pipeline runs fastqc in parallel on the input fastq files (paired or not) and then execute multiqc. A brief sequana summary report is also produced.

Rules and configuration details

Here is the latest documented configuration file to be used with the pipeline. Each rule used in the pipeline may have a section in the configuration file.

Project details

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Files for sequana-demultiplex, version 0.8.0
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