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nextflow_RS2_star

About

This repository contains a nextflow workflow treating RNAseq data. It consits of the following steps:

  • fastq (preprocessing)
  • check strandedness (determine the strandedness of the input data)
  • STAR index reference
  • split reads
  • STAR Align to reference
  • sort and convert alignement to BAM
  • merge alignements of chunks
  • cufflinks (transcript abuundance)

Input

References:

  • Reference genome (fasta)
  • reference transcriptome (fasta)
  • genome annotation (gtf) To call the check strandedness, ensembl references are necessary. Input reads:
  • paired-ends FASTQ files (single end for the moment not supported)

Output

  • Quality control file from fastp
  • transcripts abundance from cufflinks

How to run the workflow

nextflow run path/to/nextflow_RS2_star -c nextflow.config -w /path/to/workdir

How to run on the FONDA cluster:

nextflow kuberun Nine-s/nextflow_RS2_star -r main -c nextflow.config -v nextflow-ninon:/workdir

The configuration files are available in the config directory.

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  • Nextflow 100.0%