Explore Workflows
View already parsed workflows here or click here to add your own
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dfast-filelist-outputdir.cwl
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Path: cwl/workflow/dfast-filelist-outputdir.cwl Branch/Commit ID: master |
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salmon_wf_se.cwl
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Path: workflows/salmon/single_end/salmon_wf_se.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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canine_gatk_cnv_module.cwl
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Path: subworkflows/canine_gatk_cnv_module.cwl Branch/Commit ID: master |
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wf_get_peaks_trim_partial_scatter_se.cwl
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Path: cwl/wf_get_peaks_trim_partial_scatter_se.cwl Branch/Commit ID: master |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf_nonhuman.cwl Branch/Commit ID: low-vaf |
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Instac stage-in
Stage-in using Instac |
Path: instac.cwl Branch/Commit ID: master Packed ID: main |
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Create Genomic Collection for Bacterial Pipeline
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Path: genomic_source/wf_genomic_source.cwl Branch/Commit ID: 9144d08fa7f4e852498761481dceab477167fa65 |
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bulk_process.cwl
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Path: steps/bulk_process.cwl Branch/Commit ID: 5465f66 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/pipelines/pvacseq.cwl Branch/Commit ID: No_filters_detect_variants |
