Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
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exomeseq-gatk4-03-organizedirectories.cwl
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Path: subworkflows/exomeseq-gatk4-03-organizedirectories.cwl Branch/Commit ID: master |
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calculate_contamination_workflow.cwl
GATK4.1.2 Calculate tumor-normal contamination workflow |
Path: subworkflows/calculate_contamination_workflow.cwl Branch/Commit ID: master |
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Running cellranger count and lineage inference
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Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: low-vaf |
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count-lines11-extra-step-wf-noET.cwl
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Path: tests/count-lines11-extra-step-wf-noET.cwl Branch/Commit ID: main |
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wgs alignment and germline variant detection
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Path: definitions/pipelines/germline_wgs.cwl Branch/Commit ID: downsample_and_recall |
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: master |
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integrity.cwl
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Path: workflows/dnaseq/integrity.cwl Branch/Commit ID: 1.0 |
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Salmon quantification, FASTQ -> H5AD count matrix
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Path: steps/salmon-quantification.cwl Branch/Commit ID: d71be68 |
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gcaccess_from_list
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Path: task_types/tt_gcaccess_from_list.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 |
