Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_exome_mouse.cwl Branch/Commit ID: downsample_and_recall |
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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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workflow.cwl
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Path: cwl/workflow.cwl Branch/Commit ID: master |
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mut2.cwl
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Path: tests/wf/mut2.cwl Branch/Commit ID: 4642316a30a95d4f3d135c18f98477886b160094 |
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gathered exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle_gathered.cwl Branch/Commit ID: master |
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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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functional analysis prediction with InterProScan
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Path: workflows/functional_analysis.cwl Branch/Commit ID: 8515542 |
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contaminant_cleanup
This workflow detect and remove contamination from a DNA fasta file |
Path: workflows/Contamination/contaminant-cleanup.cwl Branch/Commit ID: master |
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count-lines6-wf.cwl
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Path: v1.0/v1.0/count-lines6-wf.cwl Branch/Commit ID: master |
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gcaccess_from_list
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Path: task_types/tt_gcaccess_from_list.cwl Branch/Commit ID: master |
