Workflow: merge and annotate svs with population allele freq and vep

Fetched 2025-04-23 06:59:42 GMT
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Inputs

ID Type Title Doc
vcfs File[]
sv_db File
reference String
same_type Boolean
coding_only Boolean (Optional)
cohort_name String (Optional)
same_strand Boolean
vep_plugins String[] (Optional)
vep_assembly String
synonyms_file File (Optional)
vep_cache_dir String
minimum_sv_size Integer
minimum_sv_calls Integer
custom_gnomad_vcf File (Optional)
custom_clinvar_vcf File (Optional)
estimate_sv_distance Boolean
max_distance_to_merge Integer

Steps

ID Runs Label Doc
sort_vcf
../tools/sort_vcf.cwl (CommandLineTool)
Sort VCF
merge_vcfs
../tools/survivor.cwl (CommandLineTool)
Run SURVIVOR to merge SV calls
annotate_variants
../tools/vep.cwl (CommandLineTool)
Ensembl Variant Effect Predictor
add_population_frequency
../tools/add_sv_population_frequency.cwl (CommandLineTool)
add population allele frequencies to a vcf

Outputs

ID Type Label Doc
vep_summary File
merged_annotated_vcf File
Permalink: https://w3id.org/cwl/view/git/ffab5424bb8b5905aecf6f8e2e6387da7f3df562/definitions/subworkflows/merge_svs.cwl