For RNA-seq data, from bam/fastq to AS sites files.
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  1. import "./tasks/rmats.wdl" as rmats
  2. workflow {{ project_name }} {
  3. String sample_id
  4. File b1_1
  5. File b1_2
  6. File b1_3
  7. File b2_1
  8. File b2_2
  9. File b2_3
  10. File reference_gtf_file
  11. String rmats_docker
  12. String rmats_cluster
  13. String disk_size
  14. call rmats.rmats as rmats {
  15. input:
  16. b1_1 = b1_1,
  17. b1_2 = b1_2,
  18. b1_3 = b1_3,
  19. b2_1 = b2_1,
  20. b2_2 = b2_2,
  21. b2_3 = b2_3,
  22. reference_gtf_file = reference_gtf_file,
  23. sample_id = sample_id,
  24. docker = rmats_docker,
  25. cluster = rmats_cluster,
  26. disk_size = disk_size
  27. }
  28. }