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