Workflow: Detect whitelisted variants

Fetched 2024-11-25 23:52:29 GMT
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Inputs

ID Type Title Doc
reference File
tumor_bam File
normal_bam File
min_coverage Integer
min_var_freq Float
interval_list File
whitelist_vcf File
filter_whitelist_variants Boolean

Steps

ID Runs Label Doc
bgzip
../tools/bgzip.cwl (CommandLineTool)
bgzip VCF
index
../tools/index_vcf.cwl (CommandLineTool)
vcf index
bgzip2
../tools/bgzip.cwl (CommandLineTool)
bgzip VCF
index2
../tools/index_vcf.cwl (CommandLineTool)
vcf index
decompose
../tools/vt_decompose.cwl (CommandLineTool)
run vt decompose
whitelist_filter
../tools/filter_vcf_whitelist.cwl (CommandLineTool)
Filter variants from the whitelist detector
GATK_haplotype_caller
../tools/whitelist_gatk_haplotype_caller.cwl (CommandLineTool)
HaplotypeCaller (GATK4)

Outputs

ID Type Label Doc
whitelist_variants_vcf File
Permalink: https://w3id.org/cwl/view/git/656d9ae18f164f983c5672bcf51037cd73309f4f/subworkflows/whitelist.cwl