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@@ -21,8 +21,7 @@ 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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sequenza-utils bam2seqz -gc ${gc} --fasta ${ref_dir}/${fasta} -n ${normal_bam} -t ${tumor_bam} -o $seqz --parallel $nt |
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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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# 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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@@ -33,7 +32,7 @@ task HRD { |
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sequenza-utils seqz_binning --seqz $seqz -w 200 -o $small |
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# analysis in r |
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Rscript /home/sequenza/sequenza.r '.' ${sample} |
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Rscript /home/sequenza/sequenza.r '.' ${sample} 'XY' |
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>>> |
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runtime { |