Germline & Somatic short variant discovery (SNVs + Indels) for WGS & WES.
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- task somatic {
-
- 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 <<<
- samtools mpileup -f ${ref_dir}/${fasta} -B ${normal_bam} ${tumor_bam} | java -Xmx12g -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.TN.SNP --output-indel ${sample}.VarScan.TN.INDEL --strand-filter 1
- >>>
-
- runtime {
- docker: docker
- cluster: cluster_config
- systemDisk: "cloud_ssd 40"
- dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
- }
- output {
- File varscan_snp = "${sample}.VarScan.TN.SNP.vcf"
- File varscan_indel = "${sample}.VarScan.TN.INDEL.vcf"
-
- }
- }
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