Germline & Somatic short variant discovery (SNVs + Indels) for WGS & WES.
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  1. ### Variant Calling
  2. This APP developed for germline and somatic short variant discovery (SNVs + Indels).
  3. **Accepted data**
  4. * TN matched WES for somatic variant calling
  5. * TN matched WGS for somatic variant calling
  6. * Normal-only WES for germline variant calling
  7. * Normal-only WGS for germline variant calling
  8. The datatype is judged by whether the bed file is set (i.e. the `regions` in inputs).
  9. **Supported variant callers and annotation tools**
  10. * Variant calling:
  11. * * `haplotyper` (germline)
  12. * * `tnseq`, `tnscope`, `varscan` (somatic)
  13. * Annotation: `annovar`, `vep`.
  14. * The above tools are <u>**not activated by default**</u>, which means the default setting is `false`. You need to manually set the caller to `true` in the submitted sample.csv.
  15. ### New Releases
  16. * Two annotation tools have been added.
  17. * TNhaplotyper, named as TNseq in `v0.1.0`, has beed substituted by TNhaplotyper2.
  18. * The `corealigner` step has been removed.
  19. * Some parameters' details have been changed, such as the `interval_list` has turned into `interval`.
  20. ### Getting Started
  21. We recommend using choppy system and Aliyun OSS service. The command will look like this:
  22. ```
  23. # Activate the choppy environment
  24. $ open-choppy-env
  25. # Install the APP
  26. $ choppy install YaqingLiu/variant-calling [-f]
  27. # List the parameters
  28. $ choppy samples YaqingLiu/variant-calling-latest [--no-default]
  29. # Submit you task with the `samples.csv file` and `project name`
  30. $ choppy batch YaqingLiu/variant-calling-latest samples.csv -p Project [-l project:Label]
  31. # Query the status of all tasks in the project
  32. $ choppy query -L project:Label | grep "status"
  33. ```
  34. **Please note:** The `defaults` can be forcibly replaced by the settings in `samples.csv`. Therefore, there is no need to contact me over this issue.
  35. The parameters that must need contains: sample_id,normal_fastq_1,normal_fastq_2,tumor_fastq_1,tumor_fastq_2
  36. **Please carefully check**
  37. * the reference genome you want to use is hg38 or hg19.
  38. * bed file.
  39. * the caller you want to use.
  40. * PoN VCFs for TNseq and TNscope is supported, but are need to be generated in advance.
  41. * interval padding is default 0, and you can change it.
  42. * the annotation tool is ANNOVAR or VEP.