Explore Workflows

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

Graph	Name	Retrieved From	View
	chipseq-header.cwl	https://github.com/datirium/workflows.git Path: metadata/chipseq-header.cwl Branch/Commit ID: a179b226d17177dd32a3f9d1a24a895f33c42b38
	bam_readcount workflow	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/bam_readcount.cwl Branch/Commit ID: c235dc6d623879a6c4f5fb307f545c9806eb2d23
	fastq_clean_pe.cwl	https://github.com/NCI-GDC/gdc-dnaseq-cwl.git Path: workflows/bamfastq_align/fastq_clean_pe.cwl Branch/Commit ID: 2f7c0e92e7b88b57b86602f11c595661c374008a
	Subworkflow to allow calling different SV callers which require bam files as inputs	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: f45b52a24c7b54a75368dcbab24b4eb2c5a9c75a
	functional-wf.cwl	https://github.com/common-workflow-language/cwltool.git Path: tests/checker_wf/functional-wf.cwl Branch/Commit ID: cb81b22abc52838823da9945f04d06739ab32fda
	workflow-ebisearch.cwl	https://github.com/ebi-wp/webservice-cwl.git Path: workflows/workflow-ebisearch.cwl Branch/Commit ID: 40d46a0685a85895f597cbac7b147fd95d22c6a3
	exome alignment and germline variant detection	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: f45b52a24c7b54a75368dcbab24b4eb2c5a9c75a
	mixed_library_metrics.cwl	https://github.com/nci-gdc/gdc-dnaseq-cwl.git Path: workflows/dnaseq/mixed_library_metrics.cwl Branch/Commit ID: 2f7c0e92e7b88b57b86602f11c595661c374008a
	exome alignment and germline variant detection	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: 1249b5d4e23d57ca5e3b8ad6d8e5f10ddb019f68
	xenbase-sra-to-fastq-se.cwl	https://github.com/datirium/workflows.git Path: subworkflows/xenbase-sra-to-fastq-se.cwl Branch/Commit ID: 0ddfca10c41f83bb120c7633e0db9dba7441bca0