Annotation of genetic variants detected from human genome hg19 and hg38.
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README.md 859B

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  1. ### ANNOVAR
  2. This APP developed for the annotation of VCF files.
  3. **Please take care to check that the parameter `hg` is compatible with your reference genome reference builds version.**
  4. If the type and version of database currently used in the APP does not meet your needs, please contact the developer.
  5. ### Getting Started
  6. We recommend using choppy system and Aliyun OSS service. The command will look like this:
  7. ```
  8. # Activate the choppy environment
  9. $ open-choppy-env
  10. # Install the APP
  11. $ choppy install YaqingLiu/annovar [-f]
  12. # List the parameters
  13. $ choppy samples YaqingLiu/annovar-latest [--no-default]
  14. # Submit you task with the `samples.csv file` and `project name`
  15. $ choppy batch YaqingLiu/annovar-latest samples.csv -p Project [-l project:Label]
  16. # Query the status of all tasks in the project
  17. $ choppy query -L project:Label | grep "status"
  18. ```