Infer and visualize copy number from high-throughput DNA sequencing data.
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  1. task access {
  2. File faidx
  3. File fasta
  4. String method
  5. String min_gap_size
  6. String docker
  7. String cluster_config
  8. String disk_size
  9. command <<<
  10. if [ ${method} == "wgs" ]; then
  11. cnvkit.py access -s ${min_gap_size} -o access-mappable.bed ${fasta}
  12. fi
  13. >>>
  14. runtime {
  15. docker: docker
  16. cluster: cluster_config
  17. systemDisk: "cloud_ssd 40"
  18. dataDisk: "cloud_ssd " + disk_size + " /cromwell_root/"
  19. }
  20. output {
  21. File access_bed = "access-mappable.bed"
  22. }
  23. }