从RNAseq数据中call突变
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  1. task mapping {
  2. File SAref_dir
  3. File STref_dir
  4. File fasta
  5. File fastq_1
  6. File fastq_2
  7. String sample
  8. String SAdocker
  9. String cluster_config
  10. String disk_size
  11. command <<<
  12. set -o pipefail
  13. set -e
  14. STAR --genomeDir ${SAref_dir} --readFilesIn ${fastq_1} ${fastq_2} --readFilesCommand zcat --runThreadN 20 --outFileNamePrefix OnePass_
  15. STAR --runMode genomeGenerate --genomeDir "./" --genomeFastaFiles ${STref_dir}/${fasta} --sjdbFileChrStartEnd OnePass_SJ.out.tab --sjdbOverhang 75 --runThreadN 12
  16. STAR --genomeDir "./" --readFilesIn ${fastq_1} ${fastq_2} --readFilesCommand zcat --runThreadN 20 --outFileNamePrefix ${sample}_
  17. >>>
  18. runtime {
  19. docker:SAdocker
  20. cluster: cluster_config
  21. systemDisk: "cloud_ssd 40"
  22. dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
  23. }
  24. output {
  25. File aligned_sam = "${sample}_Aligned.out.sam"
  26. }
  27. }