Automated integrated analysis software for genomics data of the cancer patients.
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vor 2 Jahren
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  1. task VarScan {
  2. String sample
  3. File normal_bam
  4. File normal_bam_index
  5. File tumor_bam
  6. File tumor_bam_index
  7. File ref_dir
  8. String fasta
  9. String docker
  10. String cluster_config
  11. String disk_size
  12. command <<<
  13. # somatic
  14. 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
  15. # processSomatic
  16. java -Xmx64g -jar /opt/VarScan.v2.4.3.jar processSomatic ${sample}.VarScan.SNP.vcf
  17. java -Xmx64g -jar /opt/VarScan.v2.4.3.jar processSomatic ${sample}.VarScan.INDEL.vcf
  18. # somaticFilter
  19. 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
  20. 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
  21. 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
  22. 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
  23. 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
  24. 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
  25. # Merge SNP and INDEL
  26. awk '{if ($1!~/^#/) print}' ${sample}.VarScan.SNP.Somatic.filter.vcf | cat ${sample}.VarScan.INDEL.Somatic.filter.vcf - > ${sample}.VarScan.Somatic.vcf
  27. awk '{if ($1!~/^#/) print}' ${sample}.VarScan.SNP.Germline.filter.vcf | cat ${sample}.VarScan.INDEL.Germline.filter.vcf - > ${sample}.VarScan.Germline.vcf
  28. awk '{if ($1!~/^#/) print}' ${sample}.VarScan.SNP.LOH.filter.vcf | cat ${sample}.VarScan.INDEL.LOH.filter.vcf - > ${sample}.VarScan.LOH.vcf
  29. >>>
  30. runtime {
  31. docker: docker
  32. cluster: cluster_config
  33. systemDisk: "cloud_ssd 40"
  34. dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
  35. }
  36. output {
  37. File varscan_snp = "${sample}.VarScan.SNP.vcf"
  38. File varscan_indel = "${sample}.VarScan.INDEL.vcf"
  39. File varscan_somatic = "${sample}.VarScan.Somatic.vcf"
  40. File varscan_germline = "${sample}.VarScan.Germline.vcf"
  41. File varscan_loh = "${sample}.VarScan.LOH.vcf"
  42. }
  43. }