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_txt_file
  5. Array[Array[File]] b1_txt = read_csv(b1_txt_file)
  6. File b2_txt_file
  7. Array[Array[File]] b2_txt = read_csv(b2_txt_file)
  8. File reference_gtf_file
  9. String rmats_docker
  10. String rmats_cluster
  11. String disk_size
  12. call rmats.rmats as rmats {
  13. input:
  14. b1_txt_file = b1_txt_file,
  15. b2_txt_file = b2_txt_file,
  16. reference_gtf_file = reference_gtf_file,
  17. sample_id = sample_id,
  18. docker = rmats_docker,
  19. cluster = rmats_cluster,
  20. disk_size = disk_size
  21. }
  22. }