Explore Workflows

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

Graph	Name	Retrieved From	View
	Hello World Outputs a message using echo	https://github.com/common-workflow-language/cwltool.git Path: tests/wf/hello-workflow.cwl Branch/Commit ID: 4a5fe26e32d244d95f9483c3edfc3df04f3e5f7b
	Apply filters to VCF file	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: a93be3183c2218ee50f13ae2675dd1cde563fdbc
	extract_readgroups_bam_http.cwl	https://github.com/nci-gdc/gdc-dnaseq-cwl.git Path: workflows/bamfastq_align/extract_readgroups_bam_http.cwl Branch/Commit ID: 20a901f44c9fb0e6f4ee3c40ec33fa4b1c8ef005
	count-lines13-wf.cwl	https://github.com/common-workflow-language/cwltool.git Path: cwltool/schemas/v1.0/v1.0/count-lines13-wf.cwl Branch/Commit ID: 875b928ce50a3202f5954843b79ea86683c160fa
	conditional_bamindex.cwl	https://github.com/NCI-GDC/gdc-dnaseq-cwl.git Path: workflows/bamfastq_align/conditional_bamindex.cwl Branch/Commit ID: 0d3fdddeae5a398e476d91aa98766965866d8eae
	scatterfail.cwl	https://github.com/common-workflow-language/cwltool.git Path: tests/wf/scatterfail.cwl Branch/Commit ID: ec2cf2da6c31ffedf827a0fb213b5204e172f510
	exome alignment and germline variant detection	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: 0805e8e0d358136468e0a9f49e06005e41965adc
	fastq_clean_se.cwl	https://github.com/nci-gdc/gdc-dnaseq-cwl.git Path: workflows/bamfastq_align/fastq_clean_se.cwl Branch/Commit ID: 17823fcd036d134df803fbf76e23b0bc5eabedfd
	module-6	https://github.com/mskcc/roslin-variant.git Path: setup/cwl/module-6.cwl Branch/Commit ID: 49d7810b6446d6aadfcdbb6b5deee9f02ad749c2
	Filter Protein Seeds I; Find ProSplign Alignments I	https://github.com/ncbi/pgap.git Path: protein_alignment/wf_compart_filter_prosplign.cwl Branch/Commit ID: be5ae41801b19ebc69a2889d8fdb39e8e2359611