Germline & Somatic short variant discovery (SNVs + Indels) for WGS & WES.
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README.md 2.1KB

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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 or tumor-only WES/WGS for somatic variant calling
  5. * Normal-only WES/WGS for germline variant calling
  6. The datatype is judged by whether the bed file is set (i.e. the `regions` in inputs).
  7. **Supported variant callers and annotation tools**
  8. * Variant calling: `haplotyper`, `pindel` (germline); `tnseq`, `tnscope`, `varscan` (somatic; `varscan` don't support the variant calling of tumor-only data).
  9. * Annotation: `annovar`, `vep`.
  10. * 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.
  11. ### New Releases
  12. * Two annotation tools have been added.
  13. * TNhaplotyper, named as TNseq in `v0.1.0`, has beed substituted by TNhaplotyper2.
  14. * The `corealigner` step has been removed.
  15. * Some parameters' details have been changed, such as the `interval_list` has turned into `interval`.
  16. ### Getting Started
  17. We recommend using choppy system and Aliyun OSS service. The command will look like this:
  18. ```
  19. # Activate the choppy environment
  20. $ open-choppy-env
  21. # Install the APP
  22. $ choppy install YaqingLiu/variant-calling [-f]
  23. # List the parameters
  24. $ choppy samples YaqingLiu/variant-calling-latest [--no-default]
  25. # Submit you task with the `samples.csv file` and `project name`
  26. $ choppy batch YaqingLiu/variant-calling-latest samples.csv -p Project [-l project:Label]
  27. # Query the status of all tasks in the project
  28. $ choppy query -L project:Label | grep "status"
  29. ```
  30. **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.
  31. The parameters that must need contains: sample_id,normal_fastq_1,normal_fastq_2,tumor_fastq_1,tumor_fastq_2
  32. **Please carefully check**
  33. * the reference genome you want to use is hg38 or hg19.
  34. * bed file.
  35. * the caller you want to use.
  36. * PoN VCFs for TNseq and TNscope is supported, but are need to be generated in advance.
  37. * interval padding is default 0, and you can change it.
  38. * usually only one annotation tool is sufficient.