This workflow performs variant calling and annotation for bulk RNA-Seq samples.
- Matteo Massidda, University of Sassari
The usage of this workflow is described in the Snakemake Workflow Catalog.
If you use this workflow in a paper, don't forget to give credits to the authors by citing the URL of this (original) repository and its DOI (see above).
Create a virtual environment with the command:
mamba create -c bioconda -c conda-forge --name snakemake snakemake=7.18.1 snakedeploy
and activate it:
conda activate snakemake
You can perform the pipeline deploy defining a directory my_dest_dir
for analysis output and a pipeline tag for a specific version:
snakedeploy deploy-workflow https://github.com/massiddamt/rna_vc_docker.git
my_desd_dir
--tag v1.0.2
To run the pipeline, go inside the deployed pipeline folder and use the command:
snakemake --use-conda -p --cores all