Automated integrated analysis software for genomics data of the cancer patients.
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- task VarScan {
-
- String sample
- File normal_bam
- File normal_bam_index
- File tumor_bam
- File tumor_bam_index
-
- File ref_dir
- String fasta
- String docker
- String cluster_config
- String disk_size
-
- command <<<
- # somatic
- samtools mpileup -f ${ref_dir}/${fasta} -B ${normal_bam} ${tumor_bam} | java -Xmx64g -jar /opt/VarScan.v2.4.3.jar somatic --mpileup 1 --min-coverage 3 --min-coverage-normal 3 --min-coverage-tumor 3 --min-var-freq 0.08 --p-value 0.10 --somatic-p-value 0.05 --output-vcf 1 --output-snp ${sample}.VarScan.SNP --output-indel ${sample}.VarScan.INDEL --strand-filter 1
-
- # processSomatic
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar processSomatic ${sample}.VarScan.SNP.vcf
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar processSomatic ${sample}.VarScan.INDEL.vcf
-
- # somaticFilter
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar somaticFilter ${sample}.VarScan.SNP.Somatic.hc.vcf --min-coverage 10 --min-reads2 2 --min-strands2 1 --min-avg-qual 20 --p-value 0.1 --indel-file ${sample}.VarScan.INDEL.vcf --output-file ${sample}.VarScan.SNP.Somatic.filter.vcf
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar somaticFilter ${sample}.VarScan.SNP.Germline.hc.vcf --min-coverage 10 --min-reads2 2 --min-strands2 1 --min-avg-qual 20 --p-value 0.1 --indel-file ${sample}.VarScan.INDEL.vcf --output-file ${sample}.VarScan.SNP.Germline.filter.vcf
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar somaticFilter ${sample}.VarScan.SNP.LOH.hc.vcf --min-coverage 10 --min-reads2 2 --min-strands2 1 --min-avg-qual 20 --p-value 0.1 --indel-file ${sample}.VarScan.INDEL.vcf --output-file ${sample}.VarScan.SNP.LOH.filter.vcf
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar somaticFilter ${sample}.VarScan.INDEL.Somatic.hc.vcf --min-coverage 10 --min-reads2 2 --min-strands2 1 --min-avg-qual 20 --p-value 0.1 --output-file ${sample}.VarScan.INDEL.Somatic.filter.vcf
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar somaticFilter ${sample}.VarScan.INDEL.Germline.hc.vcf --min-coverage 10 --min-reads2 2 --min-strands2 1 --min-avg-qual 20 --p-value 0.1 --output-file ${sample}.VarScan.INDEL.Germline.filter.vcf
- java -Xmx64g -jar /opt/VarScan.v2.4.3.jar somaticFilter ${sample}.VarScan.INDEL.LOH.hc.vcf --min-coverage 10 --min-reads2 2 --min-strands2 1 --min-avg-qual 20 --p-value 0.1 --output-file ${sample}.VarScan.INDEL.LOH.filter.vcf
-
- # Merge SNP and INDEL
- awk '{if ($1!~/^#/) print}' ${sample}.VarScan.SNP.Somatic.filter.vcf | cat ${sample}.VarScan.INDEL.Somatic.filter.vcf - > ${sample}.VarScan.Somatic.vcf
- awk '{if ($1!~/^#/) print}' ${sample}.VarScan.SNP.Germline.filter.vcf | cat ${sample}.VarScan.INDEL.Germline.filter.vcf - > ${sample}.VarScan.Germline.vcf
- awk '{if ($1!~/^#/) print}' ${sample}.VarScan.SNP.LOH.filter.vcf | cat ${sample}.VarScan.INDEL.LOH.filter.vcf - > ${sample}.VarScan.LOH.vcf
- >>>
-
- runtime {
- docker: docker
- cluster: cluster_config
- systemDisk: "cloud_ssd 40"
- dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
- }
-
- output {
- File varscan_snp = "${sample}.VarScan.SNP.vcf"
- File varscan_indel = "${sample}.VarScan.INDEL.vcf"
- File varscan_somatic = "${sample}.VarScan.Somatic.vcf"
- File varscan_germline = "${sample}.VarScan.Germline.vcf"
- File varscan_loh = "${sample}.VarScan.LOH.vcf"
- }
- }
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