Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
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1st-workflow.cwl
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https://github.com/NAL-i5K/CWL_Common-Workflow-Language.git
Path: demo_workflow4/1st-workflow.cwl Branch/Commit ID: 0aae893956e815cde58d5f04d92e44ad918ffac1 |
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allele-vcf-rnaseq-se.cwl
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https://github.com/Barski-lab/workflows.git
Path: workflows/allele-vcf-rnaseq-se.cwl Branch/Commit ID: b25b17651171f32005e9d879a9a049382f044baf |
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tt_univec_wnode.cwl
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https://github.com/ncbi/pgap.git
Path: task_types/tt_univec_wnode.cwl Branch/Commit ID: 68058b108cb5b0b72ebe244c42eefa2747e1d64a |
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downsample unaligned BAM and align
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/downsampled_alignment.cwl Branch/Commit ID: 25aa4788dd4efb1cc8ed6f609cb7803896e4d28d |
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mutect parallel workflow
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/mutect.cwl Branch/Commit ID: 60d8a9e6c5f571ec9b37f10290a1f4613013f3e1 |
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assemble.cwl
Assemble a set of reads using SKESA |
https://github.com/ncbi/pgap.git
Path: assemble.cwl Branch/Commit ID: f3bc91cf1320f75967ec2719b1506b75f23cb4b6 |
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exome alignment and somatic variant detection
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https://github.com/genome/analysis-workflows.git
Path: definitions/pipelines/somatic_exome_mouse.cwl Branch/Commit ID: 1560e7817fdb71d58aca7f98aba68809d840ade1 |
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alignment_bwa_mem.cwl
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https://github.com/uc-cdis/genomel_pipelines.git
Path: genomel/cwl/workflows/harmonization/alignment_bwa_mem.cwl Branch/Commit ID: 8b8c058848e4efe8b12e4070efec046835a19508 |
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default-dir5.cwl
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https://github.com/common-workflow-language/cwltool.git
Path: tests/wf/default-dir5.cwl Branch/Commit ID: 526f36f93655bfb098f766ff020708b5a707513a |
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Detect DoCM variants
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/docm_germline.cwl Branch/Commit ID: e509210450e4c62aecb99a228fc97f0eae2d9580 |
