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fasta_sampler.nf

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  • Forked from LBMC / nextflow
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    trimming_single.nf 541 B
    params.fastq = "$baseDir/data/fastq/*.fastq"
    
    log.info "fastq files : ${params.fastq}"
    
    Channel
      .fromPath( params.fastq )
      .ifEmpty { error "Cannot find any fastq files matching: ${params.fastq}" }
      .set { fastq_files }
    
    process trimming {
      tag "$reads.baseName"
      cpus 4
    
      input:
      file reads from fastq_files
    
      output:
      file "*_trim.fastq.gz" into fastq_files_trim
    
      script:
      """
      UrQt --t 20 --m ${task.cpus} --gz \
      --in ${reads} \
      --out ${reads.baseName}_trim.fastq.gz \
      > ${reads.baseName}_trimming_report.txt
      """
    }