Workflow: main-NA12878-platinum-chr20.cwl

Fetched 2026-10-11 23:56:59 GMT
children parents
Workflow as SVG
  • Selected
  • Default Values
  • Nested Workflows
  • Tools
  • Inputs/Outputs

Inputs

ID Type Title Doc
files 96c0eb78d9320cfb6fde870d8713f152[]
analysis String[]
vrn_file String[]
description String[]
rgnames__lb String[]
rgnames__pl String[]
rgnames__pu String[]
rgnames__rg String[]
genome_build String[]
rgnames__lane String[]
reference__rtg File[]
metadata__batch String[]
rgnames__sample String[]
reference__viral bcc15b411fa048c6dc280d9d971bc220[]
reference__snpeff File[]
metadata__phenotype String[]
config__algorithm__qc 6a86d8010c3c98b0a8f2881b2b865101[]
reference__fasta__base File[]
reference__bwa__indexes File[]
genome_resources__version Long[]
reference__genome_context c1a3cad20cbc1c17d6383fc301eb511a[]
config__algorithm__aligner String[]
config__algorithm__archive String[]
config__algorithm__effects Boolean[]
config__algorithm__realign Boolean[]
config__algorithm__tools_on e5ef9ea9fbda9a2c6969932c42c2b1c5[]
config__algorithm__validate File[]
config__algorithm__tools_off 55e6113164958030ec06ce247a3b84a6[]
config__algorithm__recalibrate Boolean[]
config__algorithm__variantcaller ac8b51d2368020ddbf3e0d86004e233f[]
genome_resources__aliases__human Boolean[]
genome_resources__rnaseq__dexseq File[]
genome_resources__variation__lcr File[]
genome_resources__aliases__snpeff String[]
genome_resources__rnaseq__refflat File[]
config__algorithm__mark_duplicates Boolean[]
config__algorithm__variant_regions String[]
genome_resources__aliases__ensembl String[]
genome_resources__variation__dbsnp File[]
config__algorithm__align_split_size String[]
config__algorithm__nomap_split_size Long[]
config__algorithm__validate_regions File[]
genome_resources__variation__cosmic String[]
config__algorithm__coverage_interval String[]
genome_resources__rnaseq__transcripts File[]
config__algorithm__nomap_split_targets Long[]
genome_resources__variation__sv_repeat File[]
genome_resources__variation__qsignature File[]
genome_resources__variation__train_omni File[]
genome_resources__variation__train_1000g File[]
genome_resources__variation__train_hapmap File[]
genome_resources__variation__train_indels File[]
genome_resources__rnaseq__transcripts_mask File[]
genome_resources__rnaseq__transcriptome_index__tophat String[]

Steps

ID Runs Label Doc
alignment
wf-alignment.cwl (Workflow)
qc_to_rec
steps/qc_to_rec.cwl (CommandLineTool)
variantcall
wf-variantcall.cwl (Workflow)
prep_samples
steps/prep_samples.cwl (CommandLineTool)
multiqc_summary
steps/multiqc_summary.cwl (CommandLineTool)
alignment_to_rec
steps/alignment_to_rec.cwl (CommandLineTool)
pipeline_summary
steps/pipeline_summary.cwl (CommandLineTool)
prep_samples_to_rec
steps/prep_samples_to_rec.cwl (CommandLineTool)
summarize_grading_vc
steps/summarize_grading_vc.cwl (CommandLineTool)
batch_for_variantcall
steps/batch_for_variantcall.cwl (CommandLineTool)
postprocess_alignment
steps/postprocess_alignment.cwl (CommandLineTool)
combine_sample_regions
steps/combine_sample_regions.cwl (CommandLineTool)
postprocess_alignment_to_rec
steps/postprocess_alignment_to_rec.cwl (CommandLineTool)

Outputs

ID Type Label Doc
align_bam File[]
summary__multiqc File[]
validate__grading_summary File[]
Permalink: https://w3id.org/cwl/view/git/b1f00f3ae914ca66aa0fa864869e934ddb69a715/NA12878-chr20/NA12878-platinum-chr20-workflow/main-NA12878-platinum-chr20.cwl