Infer and visualize copy number from high-throughput DNA sequencing data.
Nevar pievienot vairāk kā 25 tēmas Tēmai ir jāsākas ar burtu vai ciparu, tā var saturēt domu zīmes ('-') un var būt līdz 35 simboliem gara.

50 rindas
1.1KB

  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 fasta
  12. File fai
  13. String docker
  14. String cluster_config
  15. String disk_size
  16. call access.access as access {
  17. input:
  18. fasta=fasta,
  19. fai=fai,
  20. docker = docker,
  21. cluster_config = cluster_config,
  22. disk_size = disk_size
  23. }
  24. call batch.batch as batch {
  25. input:
  26. sample_id = sample_id,
  27. fasta=fasta,
  28. fai=fai,
  29. tumor_bam = tumor_bam,
  30. tumor_bai = tumor_bai,
  31. normal_bam = normal_bam,
  32. normal_bai = normal_bai,
  33. bed = bed,
  34. access_bed = access.access_bed,
  35. docker = docker,
  36. cluster_config = cluster_config,
  37. disk_size = disk_size
  38. }
  39. call export.export as export {
  40. input:
  41. result = batch.result,
  42. docker = docker,
  43. cluster_config = cluster_config,
  44. disk_size = disk_size
  45. }
  46. }