Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View | 
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                                        fillout_workflow.cwl
                                         Workflow to run GetBaseCountsMultiSample fillout on a number of bam files with a single maf file  | 
                                    
                                        
                                             Path: cwl/fillout_workflow.cwl Branch/Commit ID: dbff0c5ae06a8b21ec70bc8279f32bce151cbfc2  | 
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                                        gatk-4.0.0.0-genomics-db-and-genotypegvcfs-per-interval.cwl
                                         
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                                             Path: cwl/workflows/gatk-4.0.0.0-genomics-db-and-genotypegvcfs-per-interval.cwl Branch/Commit ID: b7aa668822c782191d0fe5641467885c023cc256  | 
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                                        trim-chipseq-pe.cwl
                                         Runs ChIP-Seq BioWardrobe basic analysis with paired-end input data files.  | 
                                    
                                        
                                             Path: workflows/trim-chipseq-pe.cwl Branch/Commit ID: 144eee15187c1a1145ce1ee0239da69059fd2752  | 
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                                        step-valuefrom2-wf.cwl
                                         
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                                             Path: cwltool/schemas/v1.0/v1.0/step-valuefrom2-wf.cwl Branch/Commit ID: 4bf61c8a3d519eefd8b9271af73974bec62535ba  | 
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                                        rnaseq-alignment-quantification
                                         This workflow retrieve SRA fastqc data and execute QC, alignment and quantification from TPMCalculator  | 
                                    
                                        
                                             Path: workflows/RNA-Seq/rnaseq-alignment-quantification.cwl Branch/Commit ID: b5a440939ac6022ee81aeeb0dd7daf3983228a61  | 
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                                        tmb_workflow.cwl
                                         Workflow to run the TMB analysis on a batch of samples and merge the results back into a single data clinical file  | 
                                    
                                        
                                             Path: cwl/tmb_workflow.cwl Branch/Commit ID: dbff0c5ae06a8b21ec70bc8279f32bce151cbfc2  | 
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                                        scRNA-seq pipeline using Salmon and Alevin
                                         
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                                             Path: pipeline.cwl Branch/Commit ID: 4c38ec433fd6fcbbe2ab659c97db729665864023  | 
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                                        count-lines1-wf.cwl
                                         
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                                             Path: cwltool/schemas/v1.0/v1.0/count-lines1-wf.cwl Branch/Commit ID: b3639a4c5075abc562b7f9b816be0d4f7d711703  | 
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                                        wgs alignment and germline variant detection
                                         
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                                             Path: definitions/pipelines/germline_wgs.cwl Branch/Commit ID: efbbe5ed51f6ac583e87a348785c72818a33f56e  | 
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                                        Tumor-Only Detect Variants workflow
                                         
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                                             Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 37a3622d1d03812e4f868b5024c52607696bfb75  | 
                                    
