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This APP developed for germline and somatic short variant discovery (SNVs + Indels).
Accepted data
The datatype is judged by whether the bed file is set (i.e. the regions
in inputs).
Supported variant callers and annotation tools
haplotyper
(germline); tnseq
, tnscope
, varscan
(somatic).annovar
, vep
.false
. You need to manually set the caller to true
in the submitted sample.csv.v0.1.0
, has beed substituted by TNhaplotyper2.corealigner
step has been removed.interval_list
has turned into interval
.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/variant-calling [-f]
# List the parameters
$ choppy samples YaqingLiu/variant-calling-latest [--no-default]
# Submit you task with the `samples.csv file` and `project name`
$ choppy batch YaqingLiu/variant-calling-latest samples.csv -p Project [-l project:Label]
# Query the status of all tasks in the project
$ choppy query -L project:Label | grep "status"
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.
The parameters that must need contains: sample_id,normal_fastq_1,normal_fastq_2,tumor_fastq_1,tumor_fastq_2
Please carefully check