sequana-ribofinder 1.1.1

Description:

sequanaribofinder 1.1.1

This is is the ribofinder pipeline from the Sequana project

Overview:
Simple parallele workflow to detect and report ribosomal content

Input:
FastQ files

Output:
HTML reports

Status:
production

Citation:
Cokelaer et al, (2017), ‘Sequana’: a Set of Snakemake NGS pipelines, Journal of Open Source Software, 2(16), 352, JOSS DOI doi:10.21105/joss.00352



Installation
Using pip from Python, just install this package:
pip install sequana_ribofinder --upgrade
The –upgrade option is to make sure you’ll get the latest version.


Usage
This pipeline scans input fastq.gz files found in the local
directory and identify the proportion of ribosomal content.
For help, please type:
sequana_ribofinder --help
The following command searches for input files in DATAPATH. Then, te user provide
a list of rRNA sequences in FastA format in test.fasta. This command creates a directory
called ribofinder/ where a snakemake pipeline can:
sequana_ribofinder --input-directory DATAPATH --rRNA-file test.fasta
You will then need to execute the pipeline:
cd ribofinder
sh ribofinder.sh # for a local run
This launch a snakemake pipeline. If you are familiar with snakemake, you can
retrieve the pipeline itself and its configuration files and then execute the pipeline yourself with specific parameters:
snakemake -s ribofinder.rules -c config.yaml --cores 4 --wrapper-prefix git+file:////home/user/sequana_wrappers
Or use sequanix interface.


Requirements
This pipelines requires the following executable(s):

bowtie1 >= 1.3.0
bedtools
samtools
bamtools
pigz




Details
This pipeline runs ribofinder in parallel on the input fastq files.
A brief sequana summary report is also produced.
You can start from the reference file and the GFF file. By default we search for the feature called
rRNA to be found in the GFF file:
sequana_ribofinder --input-directory . --reference-file genome.fasta --gff-file genome.gff
If the default feature rRNA is not found, no error is raised for now. If you know the expected feature,
you can provide it though:
sequana_ribofinder --input-directory . --reference-file genome.fasta --gff-file genome.gff --rRNA-feature gene_rRNA
If you have an existing or custom rRNA file, you can then use it as follows, in which case, no input reference is
required:
sequana_ribofinder --input-directory . --rRNA-file ribo.fasta


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.


Changelog


Version
Description



1.1.1

hotfix for running on HPC (slurm)



1.1.0

Uses click (refactoring of sequana_pipetools)



1.0.1

add sequana_wrappers in the config/pipeline



1.0.0

use graphviz apptainer and latest wrappers



0.13.0

add final apptainers and update CI actions



0.12.0

set singularity containers



0.11.1

Fix config file (removing hard-coded path)



0.11.0

Fix multiqc plot using same fix as in sequna_rnaseq pipelines
add utility plot to check rate of ribosomal per sequence and also
the corresponding RPKM.



0.10.2

Fix the bowtie1 rule (all samples were named bowtie1)



0.10.1

add additional test and fix bug in pipeline (regression bug)



0.10.0

Update to use sequana-wrappers. Remove multiqc. summary.html
is self-content



0.9.3

fix logger



0.9.2
First release.