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script7.nf
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script7.nf
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/*
* pipeline input parameters
*/
params.reads = "$baseDir/data/ggal/gut_{1,2}.fq"
params.transcript = "$baseDir/data/ggal/transcriptome.fa"
params.multiqc = "$baseDir/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 from params.transcript
output:
path 'index' into index_ch
script:
"""
salmon index --threads $task.cpus -t $transcriptome -i index
"""
}
Channel
.fromFilePairs( params.reads, checkIfExists:true )
.into { read_pairs_ch; read_pairs2_ch }
/*
* Run Salmon to perform the quantification of expression using
* the index and the matched read files
*/
process quantification {
input:
path index from index_ch
tuple val(pair_id), path(reads) from read_pairs_ch
output:
path(pair_id) into quant_ch
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 $sample_id"
input:
tuple val(sample_id), path(reads) from read_pairs2_ch
output:
path("fastqc_${sample_id}_logs") into fastqc_ch
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('*') from quant_ch.mix(fastqc_ch).collect()
output:
path('multiqc_report.html')
script:
"""
multiqc .
"""
}
workflow.onComplete {
log.info ( workflow.success ? "\nDone! Open the following report in your browser --> $params.outdir/multiqc_report.html\n" : "Oops .. something went wrong" )
}