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Merge pull request #18 from annacprice/shovill
initial commit of shovill
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20
tools/shovill/main.nf
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20
tools/shovill/main.nf
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process shovill {
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tag { shovill }
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publishDir "${params.outdir}", pattern: '*.fasta', mode: 'copy'
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container "quay.io/biocontainers/shovill:1.0.9--0"
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input:
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tuple(sample_id, path(forward), path(reverse))
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output:
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path("${sample_id}.fasta")
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script:
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"""
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shovill --R1 ${forward} --R2 ${reverse} --outdir shovill_out
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mv shovill_out/contigs.fa ${sample_id}.fasta
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"""
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}
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30
tools/shovill/meta.yml
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tools/shovill/meta.yml
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name: Shovill
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description: Create a bacterial assembly from paired fastq using shovill
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keywords:
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- Genome Assembly
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- Bacterial Isolates
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tools:
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- fastqc:
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description: |
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Shovill assembles bacterial isolate genomes from Illumina
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paired-end reads. Shovill uses the SPAdes genome assembler,
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providing pre and post-processing to the SPAdes assembly.
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It also supports SKESA, Velvet and Megahit.
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homepage: https://github.com/tseemann/shovill
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documentation: https://github.com/tseemann/shovill/blob/master/README.md
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input:
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-
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- sample_id:
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type: string
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description: Sample identifier
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- reads:
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type: file
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description: pair of fastq files
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output:
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-
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- assembly:
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type: file
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description: fasta file
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pattern: ${sample_id}.fasta
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authors:
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- @annacprice
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17
tools/shovill/test/main.nf
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tools/shovill/test/main.nf
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#!/usr/bin/env nextflow
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nextflow.preview.dsl = 2
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// import shovill
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include {shovill} from '../main.nf' params(params)
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// define input channel
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readsPath = '../../../test-datasets/tools/shovill/input/SRR3609257_{1,2}.fastq.gz'
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Channel
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.fromFilePairs( "${readsPath}", flat: true )
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.set{ ch_reads }
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// main workflow
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workflow {
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shovill(ch_reads)
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}
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5
tools/shovill/test/nextflow.config
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tools/shovill/test/nextflow.config
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// docker
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docker.enabled = true
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// output directory
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params.outdir = './results'
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