- Selected
- |
- Default Values
- Nested Workflows
- Tools
- Inputs/Outputs
This workflow is Open Source and may be reused according to the terms of:
GNU Affero General Public License v3.0
Note that the tools invoked by the workflow may have separate licenses.
Inputs
ID | Type | Title | Doc |
---|---|---|---|
bam | File [BAM] | Indexed sorted BAM with labeled duplicates | |
sample | String | Sample Name | |
reference | File [FASTA] | Reference genome | |
knownsites1 | File [VCF] | VCF of known SNPS sites for BQSR | |
knownsites2 | File [VCF] | VCF of known indel sites for BQSR | |
scattercount | String | Desired split for variant calling | |
fullintervallist | File | Full list of intervals to operate over |
Steps
ID | Runs | Label | Doc |
---|---|---|---|
gather-GVCFs |
gather-array-vcf.cwl
(CommandLineTool)
|
Gather GVCFs | |
splitintervals |
gatk-splitintervals.cwl
(CommandLineTool)
|
Create scatter interval files | |
recal-haplotypecaller |
gatk-wf-with-interval.cwl
(Workflow)
|
Variant calling workflow for given interval |
Outputs
ID | Type | Label | Doc |
---|---|---|---|
gatheredgvcf | File [VCF] | Gathered GVCF |
Permalink:
https://w3id.org/cwl/view/git/e4d896f5f94a9cf7b157cf87d5042e416649d87b/WGS-processing/cwl/helper/scatter-gatk-wf-with-interval.cwl