Explore Workflows
View already parsed workflows here or click here to add your own
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                                        genomics-workspace-transcript.cwl
                                         
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                                             Path: flow_genomicsWorkspace/genomics-workspace-transcript.cwl Branch/Commit ID: master  | 
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                                        Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
                                         
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                                             Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: low-vaf  | 
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                                        exome alignment and germline variant detection, with optitype for HLA typing
                                         
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                                             Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: downsample_and_recall  | 
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                                        EMG assembly for paired end Illumina
                                         
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                                             Path: workflows/emg-pipeline-v4-assembly-metaSPAdes.cwl Branch/Commit ID: master  | 
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                                        env-wf3.cwl
                                         
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                                             Path: tests/env-wf3.cwl Branch/Commit ID: main  | 
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                                        Whole Genome Sequence processing workflow scattered over samples
                                         <p>This is a “real-world” workflow example for processing Next Generation Sequencing (NGS) Whole Genome Sequence (WGS) data.</p> <p>You can learn more and run this workflow yourself by going through the <a href=\"https://doc.arvados.org/main/user/tutorials/wgs-tutorial.html\">Processing Whole Genome Sequences</a> walkthrough in the Arvados user guide.</p> <p>The steps of this workflow include:</p> <ol> <li>Check of fastq quality using FastQC</li> <li>Local alignment using BWA-MEM</li> <li>Variant calling in parallel using GATK Haplotype Caller</li> <li>Generation of an HTML report comparing variants against ClinVar archive</li> </ol> <p>The primary input parameter is the <b>Directory of paired FASTQ files</b>, which should contain paired FASTQ files (suffixed with _1 and _2) to be processed. The workflow scatters over the samples to process them in parallel.</p> <p>The remaining parameters are reference data used by various tools in the pipeline.</p>  | 
                                    
                                        
                                             Path: WGS-processing/cwl/wgs-processing-wf.cwl Branch/Commit ID: main  | 
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                                        pipeline.cwl
                                         
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                                             Path: pipeline.cwl Branch/Commit ID: 8c65f17  | 
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                                        if_input_is_bz2_generate_md5sum_else_return_input_chksum_json.cwl
                                         
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                                             Path: cwls/toolkit/if_input_is_bz2_generate_md5sum_else_return_input_chksum_json.cwl Branch/Commit ID: 0.4.0  | 
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                                        vecscreen_and_filter_workflow.cwl
                                         
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                                             Path: progs/vecscreen_and_filter_workflow.cwl Branch/Commit ID: main  | 
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                                        download_gtf.cwl
                                         
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                                             Path: workflow/download_gtf.cwl Branch/Commit ID: master  | 
                                    
