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