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

Fetched 2023-01-04 17:51:19 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)
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)
vep_ensembl_species String

ensembl species - Must be present in the cache directory. Examples: homo_sapiens or mus_musculus

vep_ensembl_version String

ensembl version - Must be present in the cache directory. Example: 95

estimate_sv_distance Boolean
vep_ensembl_assembly String

genome assembly to use in vep. Examples: GRCh38 or GRCm38

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/9a657bc8c462542dc7f57fba9e04dc1669f966ba/definitions/subworkflows/merge_svs.cwl