Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View | 
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                                        THOR - differential peak calling of ChIP-seq signals with replicates
                                         What is THOR? -------------- THOR is an HMM-based approach to detect and analyze differential peaks in two sets of ChIP-seq data from distinct biological conditions with replicates. THOR performs genomic signal processing, peak calling and p-value calculation in an integrated framework. For more information please refer to: ------------------------------------- Allhoff, M., Sere K., Freitas, J., Zenke, M., Costa, I.G. (2016), Differential Peak Calling of ChIP-seq Signals with Replicates with THOR, Nucleic Acids Research, epub gkw680.  | 
                                    
                                        
                                             Path: workflows/rgt-thor.cwl Branch/Commit ID: e0a30aa1ad516dd2ec0e9ce006428964b840daf4  | 
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                                        03-map-pe.cwl
                                         ATAC-seq 03 mapping - reads: PE  | 
                                    
                                        
                                             Path: v1.0/ATAC-seq_pipeline/03-map-pe.cwl Branch/Commit ID: 8d02684ae0ff27e641f3704686e3bc8b1979b854  | 
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                                        kmer_ref_compare_wnode
                                         
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                                             Path: task_types/tt_kmer_ref_compare_wnode.cwl Branch/Commit ID: b12ec8c8e832151033b9e6c0a76a3c3df18d45da  | 
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                                        Subworkflow that runs cnvkit in single sample mode and returns a vcf file
                                         
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                                             Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a  | 
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                                        mosdepth_to_coverage_QC.cwl
                                         
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                                             Path: cwl/workflows/mosdepth_to_coverage_QC.cwl Branch/Commit ID: 2d9d8ae9a789a4b037b65dd1958649023b3d35c8  | 
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                                        tt_kmer_top_n.cwl
                                         
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                                             Path: task_types/tt_kmer_top_n.cwl Branch/Commit ID: be5ae41801b19ebc69a2889d8fdb39e8e2359611  | 
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                                        exome alignment and tumor-only variant detection
                                         
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                                             Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 74647cc0f1abac4ee22950cfa89c44cf2ca3cffd  | 
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                                        exomeseq-gatk4-03-organizedirectories.cwl
                                         
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                                             Path: subworkflows/exomeseq-gatk4-03-organizedirectories.cwl Branch/Commit ID: e82f3a71183048dd6700ec6725ee526ac1a95238  | 
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                                        ROSE: rank ordering of super-enhancers
                                         Super-enhancers, consist of clusters of enhancers that are densely occupied by the master regulators and Mediator. Super-enhancers differ from typical enhancers in size, transcription factor density and content, ability to activate transcription, and sensitivity to perturbation. Use to create stitched enhancers, and to separate super-enhancers from typical enhancers using sequencing data (.bam) given a file of previously identified constituent enhancers (.gff)  | 
                                    
                                        
                                             Path: workflows/super-enhancer.cwl Branch/Commit ID: e0a30aa1ad516dd2ec0e9ce006428964b840daf4  | 
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                                        Cut-n-Run pipeline paired-end
                                         Experimental pipeline for Cut-n-Run analysis. Uses mapping results from the following experiment types: - `chipseq-pe.cwl` - `trim-chipseq-pe.cwl` - `trim-atacseq-pe.cwl` Note, the upstream analyses should not have duplicates removed  | 
                                    
                                        
                                             Path: workflows/trim-chipseq-pe-cut-n-run.cwl Branch/Commit ID: e0a30aa1ad516dd2ec0e9ce006428964b840daf4  | 
                                    
