Explore Workflows

View already parsed workflows here or click here to add your own

Graph	Name	Retrieved From	View
	scatter-wf3.cwl#main	https://github.com/common-workflow-language/common-workflow-language.git Path: v1.0/v1.0/scatter-wf3.cwl Branch/Commit ID: e67f19d8a713759d761ecad050966d1eb043b85c Packed ID: main
	Whole genome alignment and somatic variant detection	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: 06d2440d115b446c299b4ce96e8812d2f8df86ec
	super-enhancer.cwl Both `islands_file` and `islands_control_file` should be produced by the same cwl tool (iaintersect.cwl or macs2-callpeak-biowardrobe-only.cwl)	https://github.com/Barski-lab/workflows.git Path: workflows/super-enhancer.cwl Branch/Commit ID: b4b7b2e7e508be5eac639f9e323d141daf714c0d
	Detect DoCM variants	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/docm_germline.cwl Branch/Commit ID: f615832615c3b41728df8e47b72ef11e37e6a9e5
	scatterfail.cwl	https://github.com/common-workflow-language/cwltool.git Path: tests/wf/scatterfail.cwl Branch/Commit ID: 445f6b3a214f0c48317b25f7af278ae919ce5403
	varscan somatic workflow	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: ece70ac30cd87100a70f7dc64d08fa72724e9416
	cache_asnb_entries	https://github.com/ncbi/pgap.git Path: task_types/tt_cache_asnb_entries.cwl Branch/Commit ID: 001e133e0eedaf0dd8447e3f8b3cc898ec6e3e1d
	CODEX analysis pipeline using Cytokit	https://github.com/hubmapconsortium/codex-pipeline.git Path: pipeline.cwl Branch/Commit ID: 611fc64473903d892eee21a2e6df5ddc2a33e58f
	Running cellranger count and lineage inference	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: f615832615c3b41728df8e47b72ef11e37e6a9e5
	tt_fscr_calls_pass1	https://github.com/ncbi/pgap.git Path: task_types/tt_fscr_calls_pass1.cwl Branch/Commit ID: 0514ffe248dd11068a3f2268bc67b6ce5ab051d2