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revise input

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stead99 4 år sedan
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eaafbc8f29
3 ändrade filer med 8 tillägg och 1 borttagningar
  1. +2
    -0
      inputs
  2. +3
    -0
      tasks/fastqc.wdl
  3. +3
    -1
      workflow.wdl

+ 2
- 0
inputs Visa fil

@@ -1,5 +1,7 @@
{ "{{ project_name }}.read1": "{{ read1 }}",
"{{ project_name }}.read2": "{{ read2 }}",
"{{ project_name }}.disk_size": "{{ disk_size }}",
"{{ project_name }}.cluster_config": "OnDemand bcs.a2.xlarge img-ubuntu-vpc",
"{{ project_name }}.fastqc.docker": "registry.cn-shanghai.aliyuncs.com/pgx-docker-registry/fastqc:v0.11.5",
"{{ project_name }}.fastqscreen.docker": "registry.cn-shanghai.aliyuncs.com/pgx-docker-registry/fastqscreen:0.12.0",
"{{ project_name }}.screen_ref_dir": "/data/home/shangjun/JS_data/source_tree/source_tree/project_code/choppy_app/reference/fastq_screen_reference/",

+ 3
- 0
tasks/fastqc.wdl Visa fil

@@ -13,6 +13,9 @@ task fastqc {

runtime {
docker:docker
systemDisk:"cloud_ssd 40"
cluster:cluster_config
dataDisk:"cloud_ssd " + disk_size + " /cromwell_root/"
}
output {
File read1_html = sub(basename(read1), "\\.(fastq|fq)\\.gz$", "_fastqc.html")

+ 3
- 1
workflow.wdl Visa fil

@@ -10,13 +10,15 @@ workflow {{ project_name }} {
call fastqc.fastqc as fastqc {
input:
read1=read1,
read2=read2
read2=read2,
docker=fastqc.docker
}

call fastqscreen.fastq_screen as fastqscreen {
input:
read1=read1,
read2=read2,
docker=fastqscreen.docker,
screen_ref_dir=screen_ref_dir,
fastq_screen_conf=fastq_screen_conf
}

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