Note
If you are new to Nextflow and nf-core, please refer to this page on how to set-up Nextflow.
To run the pipeline, you will need the following:
- Sample Sheet:
A sample sheet that contains the necessary information about your sequencing samples. Here is an example of a sample sheet for a single paired-end sample:
id,r1,r2 test,test_1.fastq.gz,test_2.fastq.gz - Reference Genome: The genome sequence in FASTA format.
- Gene Annotation File: A gene annotation file in GTF format.
Once you have the required files, you can run the pipeline with the following command:
nextflow run tyfu-cc/rnaseq \
--input /path/to/sampleshee.csv \
--outdir /path/to/where/the/outputs/are/stored \
--fasta /path/to/genome.fa \
--gtf /path/to/genes.gtfSee detailed usage here.