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更新 'tasks/HRD.wdl'

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1 mainītis faili ar 2 papildinājumiem un 3 dzēšanām
  1. +2
    -3
      tasks/HRD.wdl

+ 2
- 3
tasks/HRD.wdl Parādīt failu

@@ -21,8 +21,7 @@ task HRD {
small=${sample}'.small.seqz.gz'
# bam2seqz
# sequenza-utils bam2seqz -gc ${gc} --fasta ${ref_dir}/${fasta} -n ${normal_bam} -t ${tumor_bam} -o $seqz -C chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20 chr21 chr22 chrX chrY --parallel 24
sequenza-utils bam2seqz -gc ${gc} --fasta ${ref_dir}/${fasta} -n ${normal_bam} -t ${tumor_bam} -o $seqz --parallel $nt
sequenza-utils bam2seqz -gc ${gc} --fasta ${ref_dir}/${fasta} -n ${normal_bam} -t ${tumor_bam} -o $seqz -C chr1 chr2 chr3 chr4 chr5 chr6 chr7 chr8 chr9 chr10 chr11 chr12 chr13 chr14 chr15 chr16 chr17 chr18 chr19 chr20 chr21 chr22 chrX chrY --parallel 24
# merge and remove
zcat ${sample}_*.seqz.gz | awk '{if (NR == 1 || (NR != 1 && $1 != "chromosome")) {print $0}}' | bgzip > $seqz
@@ -33,7 +32,7 @@ task HRD {
sequenza-utils seqz_binning --seqz $seqz -w 200 -o $small
# analysis in r
Rscript /home/sequenza/sequenza.r '.' ${sample}
Rscript /home/sequenza/sequenza.r '.' ${sample} 'XY'
>>>
runtime {

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