Infer and visualize copy number from high-throughput DNA sequencing data.
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  1. import "./tasks/access.wdl" as access
  2. import "./tasks/batch.wdl" as batch
  3. import "./tasks/export.wdl" as export
  4. workflow {{ project_name }} {
  5. String sample_id
  6. Array[File] tumor_bam
  7. Array[File] tumor_bai
  8. Array[File] normal_bam
  9. Array[File] normal_bai
  10. File bed
  11. File faidx
  12. File fasta
  13. File ref_flat
  14. String docker
  15. String cluster_config
  16. String disk_size
  17. call access.access as access {
  18. input:
  19. fasta = fasta,
  20. faidx = faidx,
  21. docker = docker,
  22. cluster_config = cluster_config,
  23. disk_size = disk_size
  24. }
  25. call batch.batch as batch {
  26. input:
  27. sample_id = sample_id,
  28. fasta = fasta,
  29. faidx = faidx,
  30. ref_flat = ref_flat,
  31. tumor_bam = tumor_bam,
  32. tumor_bai = tumor_bai,
  33. normal_bam = normal_bam,
  34. normal_bai = normal_bai,
  35. bed = bed,
  36. access_bed = access.access_bed,
  37. docker = docker,
  38. cluster_config = cluster_config,
  39. disk_size = disk_size
  40. }
  41. call export.export as export {
  42. input:
  43. sample_id = sample_id,
  44. results = batch.results,
  45. docker = docker,
  46. cluster_config = cluster_config,
  47. disk_size = disk_size
  48. }
  49. }