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GAGA_Metagenome.nf
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/*
* pipeline input parameters
*/
// ls -l | gawk 'match($0, /.* ([A-Z]+.[0-9]+).*/, a) {print a[1]}' will generate genome_id
params.genome =
params.reads = "$baseDir/data/ggal/gut_{1,2}.fq"
params.transcriptome = "$baseDir/data/ggal/transcriptome.fa"
params.multiqc = "$baseDir/multiqc"
params.outdir = "results"
log.info """\
GAGA Metagenome - N F P I P E L I N E
===================================
transcriptome: ${params.transcriptome}
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.transcriptome
output:
path 'index' into index_ch
script:
"""
salmon index --threads $task.cpus -t $transcriptome -i index
"""
}
Channel
.fromFilePairs( params.reads, checkIfExists: true )
.into { read_pairs_ch; read_pairs2_ch }
process quantification {
tag "$pair_id"
input:
path index from index_ch
tuple 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
"""
}
process fastqc {
tag "FASTQC on $sample_id"
input:
tuple sample_id, path(reads) from read_pairs2_ch
output:
path "fastqc_${sample_id}_logs" into fastqc_ch
script:
"""
mkdir fastqc_${sample_id}_logs
fastqc -o fastqc_${sample_id}_logs -f fastq -q ${reads}
"""
}
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" )
}