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script6.nf
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script6.nf
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/*
* This code enables the new dsl of Nextflow.
*/
nextflow.enable.dsl=2
/*
* pipeline input parameters
*/
params.reads = "$projectDir/data/ggal/gut_{1,2}.fq"
params.transcript = "$projectDir/data/ggal/transcriptome.fa"
params.multiqc = "$projectDir/multiqc"
params.outdir = "results"
log.info """\
R N A S E Q - N F P I P E L I N E
===================================
transcriptome: ${params.transcript}
reads : ${params.reads}
outdir : ${params.outdir}
"""
.stripIndent()
/*
* define the `index` process that create a binary index
* given the transcriptome file
*/
process index {
input:
path transcriptome
output:
path 'index'
script:
"""
salmon index --threads $task.cpus -t $transcriptome -i index
"""
}
/*
* Run Salmon to perform the quantification of expression using
* the index and the matched read files
*/
process quantification {
input:
path index
tuple val(pair_id), path(reads)
output:
path(pair_id)
script:
"""
salmon quant --threads $task.cpus --libType=U -i $index -1 ${reads[0]} -2 ${reads[1]} -o $pair_id
"""
}
/*
* Run fastQC to check quality of reads files
*/
process fastqc {
tag "FASTQC on $sample_id"
input:
tuple val(sample_id), path(reads)
output:
path("fastqc_${sample_id}_logs")
script:
"""
mkdir fastqc_${sample_id}_logs
fastqc -o fastqc_${sample_id}_logs -f fastq -q ${reads}
"""
}
/*
* Create a report using multiQC for the quantification
* and fastqc processes
*/
process multiqc {
publishDir params.outdir, mode:'copy'
input:
path('*')
output:
path('multiqc_report.html')
script:
"""
multiqc .
"""
}
read_pairs_ch = Channel.fromFilePairs( params.reads, checkIfExists:true )
workflow {
index( params.transcript )
quantification( index.out, read_pairs_ch )
fastqc( read_pairs_ch )
multiqc( quantification.out.mix(fastqc.out).collect() )
}