Infer and visualize copy number from high-throughput DNA sequencing data.
Vous ne pouvez pas sélectionner plus de 25 sujets Les noms de sujets doivent commencer par une lettre ou un nombre, peuvent contenir des tirets ('-') et peuvent comporter jusqu'à 35 caractères.

59 lignes
1.4KB

  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. bed = bed,
  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. segment_method = segment_method,
  38. reference = reference,
  39. tumor_bam = tumor_bam,
  40. normal_bam = normal_bam,
  41. bed = bed,
  42. access_bed = access.access_bed,
  43. docker = docker,
  44. cluster_config = cluster_config,
  45. disk_size = disk_size
  46. }
  47. call export.export as export {
  48. input:
  49. sample_id = sample_id,
  50. results = batch.results,
  51. docker = docker,
  52. cluster_config = cluster_config,
  53. disk_size = disk_size
  54. }
  55. }