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 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. docker = docker,
  24. cluster_config = cluster_config,
  25. disk_size = disk_size
  26. }
  27. call batch.batch as batch {
  28. input:
  29. sample_id = sample_id,
  30. fasta = fasta,
  31. faidx = faidx,
  32. ref_flat = ref_flat,
  33. method = method,
  34. reference = reference,
  35. tumor_bam = tumor_bam,
  36. tumor_bai = tumor_bai,
  37. normal_bam = normal_bam,
  38. normal_bai = normal_bai,
  39. bed = bed,
  40. access_bed = access.access_bed,
  41. docker = docker,
  42. cluster_config = cluster_config,
  43. disk_size = disk_size
  44. }
  45. call export.export as export {
  46. input:
  47. sample_id = sample_id,
  48. results = batch.results,
  49. docker = docker,
  50. cluster_config = cluster_config,
  51. disk_size = disk_size
  52. }
  53. }