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@@ -8,6 +8,7 @@ task HRD { |
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File tumor_bam_index |
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File? normal_bam |
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File? normal_bam_index |
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File? bed_file |
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String docker |
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String cluster_config |
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String disk_size |
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@@ -21,16 +22,23 @@ task HRD { |
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small=${sample}'.small.seqz.gz' |
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# bam2seqz |
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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 |
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if [ ${normal_bam} ]; then |
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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 |
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else |
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sequenza-utils bam2seqz -gc ${gc} --fasta ${ref_dir}/${fasta} -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 |
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fi |
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# merge and remove |
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zcat ${sample}_*.seqz.gz | awk '{if (NR == 1 || (NR != 1 && $1 != "chromosome")) {print $0}}' | bgzip > $seqz |
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tabix -f -s 1 -b 2 -e 2 -S 1 $seqz |
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rm ${sample}_*.seqz.gz; rm ${sample}_*.seqz.gz.tbi |
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# seqz_binning: WES: 50; WGS: 200 |
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sequenza-utils seqz_binning --seqz $seqz -w 200 -o $small |
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if [ ${bed_file} ]; then |
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sequenza-utils seqz_binning --seqz $seqz -w 50 -o $small |
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else |
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sequenza-utils seqz_binning --seqz $seqz -w 200 -o $small |
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fi |
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# analysis in r |
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Rscript /home/sequenza/sequenza.r '.' ${sample} 'XY' |
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>>> |