Infer and visualize copy number from high-throughput DNA sequencing data.
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README.md 1.1KB

4 vuotta sitten
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  1. # CNVkit
  2. > Author: Yaqing Liu
  3. >
  4. > E-mail:yaqing.liu@outlook.com
  5. >
  6. ## Install
  7. ```
  8. # activate choppy environment
  9. open-choppy-env
  10. # install app
  11. choppy install YaqingLiu/CNVkit
  12. ```
  13. ## Copy number calling pipeline
  14. ![image](https://cnvkit.readthedocs.io/en/stable/_images/workflow.png)
  15. ## Input
  16. ```json
  17. {
  18. "tumor_bam": [
  19. "oss://choppy-cromwell-result/...bam",
  20. "oss://choppy-cromwell-result/...bam",
  21. "oss://choppy-cromwell-result/...bam"
  22. ],
  23. "tumor_bai": [
  24. "oss://choppy-cromwell-result/...bai",
  25. "oss://choppy-cromwell-result/...bai",
  26. "oss://choppy-cromwell-result/...bai"
  27. ],
  28. "normal_bam": [
  29. "oss://choppy-cromwell-result/...bam",
  30. "oss://choppy-cromwell-result/...bam",
  31. "oss://choppy-cromwell-result/...bam"
  32. ],
  33. "normal_bai": [
  34. "oss://choppy-cromwell-result/...bai",
  35. "oss://choppy-cromwell-result/...bai",
  36. "oss://choppy-cromwell-result/...bai"
  37. ],
  38. "sample_id": "..."
  39. }
  40. ```
  41. #### Output
  42. A segment file and some intermediate *.cnn/cns will be generated, and the segment file can be imported into IGV.