Workflow: scatter GATK HaplotypeCaller over intervals
Fetched 2024-05-18 21:23:02 GMT
Verified with cwltool version 3.1.20221201130942
- Selected
- |
- Default Values
- Nested Workflows
- Tools
- Inputs/Outputs
This workflow is Open Source and may be reused according to the terms of:
MIT License
Note that the tools invoked by the workflow may have separate licenses.
Inputs
| ID | Type | Title | Doc |
|---|---|---|---|
| bam | File | ||
| dbsnp_vcf | File (Optional) | ||
| intervals | 0de87bb9b02f1b8dae3134ebb08d1fc7[] | ||
| reference | File | ||
| read_filter | String (Optional) | ||
| gvcf_gq_bands | String[] | ||
| output_prefix | String (Optional) |
an optional string to prepend to the output filename |
|
| variant_index_type | |||
| max_alternate_alleles | Integer (Optional) | ||
| contamination_fraction | String (Optional) | ||
| variant_index_parameter | String (Optional) | ||
| emit_reference_confidence |
Steps
| ID | Runs | Label | Doc |
|---|---|---|---|
| haplotype_caller |
../tools/gatk_haplotype_caller.cwl
(CommandLineTool)
|
GATK HaplotypeCaller |
Outputs
| ID | Type | Label | Doc |
|---|---|---|---|
| gvcf | File[] |
Permalink:
https://w3id.org/cwl/view/git/233f026ffce240071edda526391be0c03186fce8/definitions/subworkflows/gatk_haplotypecaller_iterator.cwl
