Explore Workflows

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

Graph	Name	Retrieved From	View
	Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 2ae0a374fab650757cdae4391c8cbd32f02edf97
	wgs alignment and tumor-only variant detection	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/tumor_only_wgs.cwl Branch/Commit ID: 9e5f228bc1a3d0dfe950b5d41d7e4319e834a6d4
	sec-wf-out.cwl	https://github.com/common-workflow-language/cwltool.git Path: tests/wf/sec-wf-out.cwl Branch/Commit ID: d7481d03fa4b5b4630392540f598acfb100b421d
	rnaediting1strand.cwl	https://github.com/YeoLab/sailor.git Path: cwl/rnaediting1strand.cwl Branch/Commit ID: 5eb7864dd3622552dc95a927d3eb6ccf5f107745
	Varscan Workflow	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: c625e05eefb1754353c1bdfa46c01dc61e6233dd
	Tumor-Only Detect Variants workflow	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 457e101e3fb87e7fd792357afce00ed8ccbfbcdb
	Prepare user input Prepare user input for NCBI-PGAP pipeline	https://github.com/ncbi/pgap.git Path: prepare_user_input2.cwl Branch/Commit ID: 7c8eb4d23c3c9859f57421643710c0b6d57b606c
	Identifies non-coding RNAs using Rfams covariance models	https://github.com/mscheremetjew/workflow-is-cwl.git Path: workflows/cmsearch-multimodel-wf.cwl Branch/Commit ID: 0be3513056e3ebbf7eac38bc1f066d846414bd6d
	collate_unique_SSU_headers.cwl	https://github.com/proteinswebteam/ebi-metagenomics-cwl.git Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: 5dc7c5ca618a248a99bd4bf5f3042cdb21947193
	collate_unique_SSU_headers.cwl	https://github.com/EBI-Metagenomics/ebi-metagenomics-cwl.git Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: 25129f55226dee595ef941edc24d3c44414e0523