Infer and visualize copy number from high-throughput DNA sequencing data.
選択できるのは25トピックまでです。 トピックは、先頭が英数字で、英数字とダッシュ('-')を使用した35文字以内のものにしてください。

61 行
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] 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. bed = bed,
  27. docker = docker,
  28. cluster_config = cluster_config,
  29. disk_size = disk_size
  30. }
  31. call batch.batch as batch {
  32. input:
  33. sample_id = sample_id,
  34. fasta = fasta,
  35. faidx = faidx,
  36. ref_flat = ref_flat,
  37. method = method,
  38. reference = reference,
  39. tumor_bam = tumor_bam,
  40. tumor_bai = tumor_bai,
  41. normal_bam = normal_bam,
  42. normal_bai = normal_bai,
  43. bed = bed,
  44. access_bed = access.access_bed,
  45. docker = docker,
  46. cluster_config = cluster_config,
  47. disk_size = disk_size
  48. }
  49. call export.export as export {
  50. input:
  51. sample_id = sample_id,
  52. results = batch.results,
  53. docker = docker,
  54. cluster_config = cluster_config,
  55. disk_size = disk_size
  56. }
  57. }