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. File? reference
  15. String min_gap_size
  16. String method
  17. String docker
  18. String cluster_config
  19. String disk_size
  20. call access.access as access {
  21. input:
  22. fasta = fasta,
  23. faidx = faidx,
  24. method = method,
  25. min_gap_size = min_gap_size,
  26. docker = docker,
  27. cluster_config = cluster_config,
  28. disk_size = disk_size
  29. }
  30. call batch.batch as batch {
  31. input:
  32. sample_id = sample_id,
  33. fasta = fasta,
  34. faidx = faidx,
  35. ref_flat = ref_flat,
  36. method = method,
  37. reference = reference,
  38. tumor_bam = tumor_bam,
  39. tumor_bai = tumor_bai,
  40. normal_bam = normal_bam,
  41. normal_bai = normal_bai,
  42. bed = bed,
  43. access_bed = access.access_bed,
  44. docker = docker,
  45. cluster_config = cluster_config,
  46. disk_size = disk_size
  47. }
  48. call export.export as export {
  49. input:
  50. sample_id = sample_id,
  51. results = batch.results,
  52. docker = docker,
  53. cluster_config = cluster_config,
  54. disk_size = disk_size
  55. }
  56. }