from fastq to bam files
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  1. task samtools {
  2. File sam
  3. String sample_id
  4. String bam = sample_id + ".bam"
  5. String sorted_bam = sample_id + ".sorted.bam"
  6. String percent_bam = sample_id + ".percent.bam"
  7. String sorted_bam_index = sample_id + ".sorted.bam.bai"
  8. String ins_size = sample_id + ".ins_size"
  9. String docker
  10. String cluster
  11. String disk_size
  12. Int insert_size
  13. command <<<
  14. set -o pipefail
  15. set -e
  16. /opt/conda/bin/samtools view -bS ${sam} > ${bam}
  17. /opt/conda/bin/samtools sort -m 1000000000 ${bam} -o ${sorted_bam}
  18. /opt/conda/bin/samtools index ${sorted_bam}
  19. /opt/conda/bin/samtools view -bs 42.1 ${sorted_bam} > ${percent_bam}
  20. /opt/conda/bin/samtools stats -i ${insert_size} ${sorted_bam} |grep ^IS|cut -f 2- > ${sample_id}.ins_size
  21. >>>
  22. runtime {
  23. docker: docker
  24. cluster: cluster
  25. systemDisk: "cloud_ssd 40"
  26. dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
  27. }
  28. output {
  29. File out_bam = sorted_bam
  30. File out_percent = percent_bam
  31. File out_bam_index = sorted_bam_index
  32. File out_ins_size = ins_size
  33. }
  34. }