Getting Started¶
First - ‘Preparing Your Account’ and ‘Miniconda’ installation instructions. All the necessary information about the pipeline is in https://github.com/BleekerLab/snakemake_rnaseq.
Go to your personal directory
cd ~/personal
Download the preprocessing pipeline from github
git clone https://github.com/BleekerLab/snakemake_rnaseq
Go to snakemake folder
cd snakemake_rnaseq/
Installation¶
Install mamba to install the environment faster (than using conda) .. code-block:: shell
conda install -c conda-forge mamba
Create the environment .. code-block:: shell
mamba env create –name rnaseq –file environment.yaml
To adjust the pipeline to your experiment, you need to modify some parameters.
For this you can either use a text editor for example gedit or you can download it using an ssh client like Filezilla and open it on your own machine.
The former is recommended. If you do the latter, make sure to upload the modified file and replace it.
Reference Genome and Annotation gtf files
In the ‘config/refs’ folder, add the reference genome and the annotation file of your choice. Then change the name of the files in the ‘config.yaml’ file, adding the path to it. eg.:
refs:
genome: "config/refs/hg38.analysisSet.fa"
gtf: "config/refs/gencode.v37.annotation.gtf"
Sample file
Make sure to replace the example config/samples.tsv file with the one relevant to your own experiment. This should include at least 3 columns: sample, fq1 and fq2.