Explore Workflows
View already parsed workflows here or click here to add your own
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varscan somatic workflow
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Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: master |
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deal_with_functional_annotation.cwl
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Path: workflows/subworkflows/assembly/deal_with_functional_annotation.cwl Branch/Commit ID: master |
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find_hotspots_in_normals.cwl
Workflow to find hotspot VAFs from duplex (for Tumor sample) and unfiltered (for Normal sample) pileups. These inputs are all required to be sorted in the same order: sample_ids patient_ids sample_classes unfiltered_pileups duplex_pileups |
Path: workflows/subworkflows/find_hotspots_in_normals.cwl Branch/Commit ID: master |
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md_launch_mutate.cwl
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Path: md_launch_mutate.cwl Branch/Commit ID: main |
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bam_filtering
BAM filtering |
Path: structuralvariants/cwl/subworkflows/bam_filtering.cwl Branch/Commit ID: 1.0.7 |
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cram_to_bam workflow
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Path: definitions/subworkflows/cram_to_bam_and_index.cwl Branch/Commit ID: low-vaf |
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: master |
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SNV background error suppression using panel of normals
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Path: subworkflows/suppress_background_error.cwl Branch/Commit ID: master |
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step3: create STAR index
create STAR index for mapping CAGE-Seq data (step 1: decompress reference genome fasta file, step 2: create STAR index) |
Path: workflow/02_star_index_subworkflow.cwl Branch/Commit ID: main |
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wf-variantcall.cwl
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Path: NA12878-chr20/NA12878-platinum-chr20-workflow-arvados/wf-variantcall.cwl Branch/Commit ID: master |
