Annotation of genetic variants detected from human genome hg19 and hg38.
Vous ne pouvez pas sélectionner plus de 25 sujets Les noms de sujets doivent commencer par une lettre ou un nombre, peuvent contenir des tirets ('-') et peuvent comporter jusqu'à 35 caractères.
YaqingLiu 17a6f2ef49 alter annotation db il y a 3 ans
tasks alter annotation db il y a 3 ans
.DS_Store first commit il y a 4 ans
LICENSE.md first commit il y a 4 ans
README.md Update: README il y a 4 ans
defaults Update il y a 4 ans
inputs Update il y a 4 ans
workflow.wdl Update il y a 4 ans

README.md

ANNOVAR

This APP developed for the annotation of VCF files.

Please take care to check that the parameter hg is compatible with your reference genome reference builds version.

If the type and version of database currently used in the APP does not meet your needs, please contact the developer.

Getting Started

We recommend using choppy system and Aliyun OSS service. The command will look like this:

# Activate the choppy environment
$ open-choppy-env

# Install the APP
$ choppy install YaqingLiu/annovar [-f]

# List the parameters
$ choppy samples YaqingLiu/annovar-latest [--no-default]

# Submit you task with the `samples.csv file` and `project name`
$ choppy batch YaqingLiu/annovar-latest samples.csv -p Project [-l project:Label]

# Query the status of all tasks in the project
$ choppy query -L project:Label | grep "status"