Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View | 
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                                        harmonization_bwa_mem.cwl
                                         
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                                             Path: genomel/cwl/workflows/harmonization/harmonization_bwa_mem.cwl Branch/Commit ID: c661469505c606e1353f23c21a6654724a9d8d63  | 
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                                        alignment_prep.cwl
                                         
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                                             Path: genomel/cwl/workflows/harmonization/alignment_prep.cwl Branch/Commit ID: c661469505c606e1353f23c21a6654724a9d8d63  | 
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                                        tt_fscr_calls_pass1
                                         
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                                             Path: task_types/tt_fscr_calls_pass1.cwl Branch/Commit ID: b38b0070edf910984f29a4a495b5dfa525b8b305  | 
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                                        count-lines1-wf.cwl
                                         
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                                             Path: tests/count-lines1-wf.cwl Branch/Commit ID: a0f2d38e37ff51721fdeaf993bb2ab474b17246b  | 
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                                        Varscan Workflow
                                         
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                                             Path: definitions/subworkflows/varscan_pre_and_post_processing.cwl Branch/Commit ID: f42c889734c8f709ad2fd9090493bcaac8326c98  | 
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                                        duplicated_readgroup_fix.cwl
                                         
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                                             Path: genomel/cwl/workflows/utils/duplicated_readgroup_fix.cwl Branch/Commit ID: c661469505c606e1353f23c21a6654724a9d8d63  | 
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                                        somatic_exome: exome alignment and somatic variant detection
                                         somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml  | 
                                    
                                        
                                             Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: a08de598edc04f340fdbff76c9a92336a7702022  | 
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                                        Detect Variants workflow
                                         
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                                             Path: definitions/pipelines/detect_variants_nonhuman.cwl Branch/Commit ID: 2e0562a5c3cd7aac24af4c622a5ae68a7fb23a71  | 
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                                        GATK4_SomaticVariantCaller_4_1_3_0.cwl
                                         
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                                             Path: janis_pipelines/wgs_somatic/cwl/tools/GATK4_SomaticVariantCaller_4_1_3_0.cwl Branch/Commit ID: 2743f22a7ffda13ac411fc1d6baa865b7c914a2b  | 
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                                        workflow.cwl
                                         
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                                             Path: flow_dispatch/2working_files/workflow.cwl Branch/Commit ID: b0c37f33a2821244526f7caa2567128bc165250b  | 
                                    
