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rna-ex6.nf
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rna-ex6.nf
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/*
* Defines some parameters in order to specify the refence genomes
* and read pairs by using the command line options
*/
params.reads = "$baseDir/data/ggal/reads/ggal_gut_{1,2}.fq"
params.annot = "$baseDir/data/ggal/annotation.gff"
params.genome = "$baseDir/data/ggal/genome.fa"
/*
* prints user convenience
*/
println "R N A T O Y P I P E L I N E "
println "================================="
println "genome : ${params.genome}"
println "annotat : ${params.annot}"
println "reads : ${params.reads}"
/*
* get a file object for the given param string
*/
genome_file = file(params.genome)
annotation_file = file(params.annot)
/*
* Step 1. Builds the genome index required by the mapping process
*/
process buildIndex {
input:
file genome from genome_file
output:
file 'genome.index*' into genome_index
"""
bowtie2-build --threads ${task.cpus} ${genome} genome.index
"""
}
/*
* Create the `read_pairs` channel that emits tuples containing three elements:
* the pair ID, the first read-pair file and the second read-pair file
*/
read_pairs = Channel.fromFilePairs(params.reads, flat: true)
/*
* Step 2. Maps each read-pair by using Tophat2 mapper tool
*/
process mapping {
input:
file 'genome.index.fa' from genome_file
file genome_index from genome_index
set pair_id, file(read1), file(read2) from read_pairs
output:
set pair_id, "tophat_out/accepted_hits.bam" into bam
"""
tophat2 -p ${task.cpus} genome.index ${read1} ${read2}
"""
}
/*
* Step 3. Assembles the transcript by using the "cufflinks" tool
*/
process makeTranscript {
publishDir "results", mode: 'copy'
input:
file annot from annotation_file
set pair_id, file(bam_file) from bam
output:
set pair_id, file('transcript_*.gtf') into transcripts
"""
cufflinks --no-update-check -q -p ${task.cpus} -G $annot ${bam_file}
mv transcripts.gtf transcript_${pair_id}.gtf
"""
}