haplotyper-battle-royale/main.nf

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#!/usr/bin/env nextflow
include { EFETCH } from './modules/efetch'
include { HAPLINK_HAPLOTYPES as HAPLINK_ML_HAPLOTYPES } from './modules/haplink/haplotypes'
include { HAPLINK_HAPLOTYPES as HAPLINK_RAW_HAPLOTYPES } from './modules/haplink/haplotypes'
include { HAPLINK_VARIANTS } from './modules/haplink/variants'
include { MINIMAP2 } from './modules/minimap2'
include { NANOFILT } form './modules/nanofilt'
include { SHORAH_AMPLICON } from './modules/shorah/amplicon'
include { SHORAH_SHOTGUN } from './modules/shorah/shotgun'
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include { VIQUAS } from './modules/viquas'
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workflow {
Channel
.fromPath("*.fastq.gz")
.map { file -> tuple(file.simpleName, file) }
.set { ch_input }
EFETCH('NC_036618.1')
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EFETCH
.out
.set { ch_reference }
NANOFILT( ch_input )
NANOFILT
.out
.set { ch_reads }
MINIMAP2( ch_reads, ch_reference )
MINIMAP2
.out
.set { ch_alignments }
HAPLINK_VARIANTS( ch_alignments, ch_reference )
HAPLINK_VARIANTS
.out
.set { ch_variants }
ch_alignments
.join( ch_variants )
.set { ch_haplotype_calling }
HAPLINK_RAW_HAPLOTYPES(
ch_haplotype_calling,
ch_reference
)
HAPLINK_RAW_HAPLOTYPES
.out
.map{ [ it[0], 'raw', it[1] ] }
.set{ ch_raw_haplotypes }
HAPLINK_ML_HAPLOTYPES(
ch_haplotype_calling,
ch_reference
)
HAPLINK_ML_HAPLOTYPES
.out
.map{ [ it[0], 'ml', it[1] ] }
.set{ ch_ml_haplotypes }
ch_raw_haplotypes
.mix(ch_ml_haplotypes)
.set{ ch_all_haplotypes }
HAPLINK_SEQUENCES(
ch_all_haplotypes,
ch_reference
)
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VIQUAS(
ch_alignments,
ch_reference
)
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}
process HAPLINK_SEQUENCES {
cpus 1
memory '6.GB'
input:
tuple val(prefix), val(method), path(yaml)
path reference
output:
tuple val(prefix), val(method), path("*.fasta")
publishDir "results/${method}-haplotypes", mode: 'copy'
script:
"""
export JULIA_NUM_THREADS=${task.cpus}
haplink sequences \\
"${reference}" \\
"${yaml}" \\
--prefix "${prefix}" \\
> "${prefix}.fasta"
"""
}