Infer and visualize copy number from high-throughput DNA sequencing data.
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  1. task batch {
  2. String sample_id
  3. File tumor_bam
  4. File tumor_bai
  5. File normal_bam
  6. File normal_bai
  7. String bed
  8. File ref_dir
  9. String fasta
  10. File access_bed
  11. String docker
  12. String cluster_config
  13. String disk_size
  14. command <<<
  15. cnvkit.py batch ${tumor_bam} --normal ${normal_bam} \
  16. --targets ${bed} \
  17. --fasta ${ref_dir}/${fasta} --access ${access_bed} \
  18. --output-reference my_reference.cnn --output-dir ./results/ \
  19. --diagram --scatter
  20. >>>
  21. runtime {
  22. docker: docker
  23. cluster: cluster_config
  24. systemDisk: "cloud_ssd 40"
  25. dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
  26. }
  27. output {
  28. File reference_cnn = "my_reference.cnn"
  29. Array[File] result = glob("result/*")
  30. }
  31. }