Explore Workflows

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

Graph	Name	Retrieved From	View
	extract_gencoll_ids	https://github.com/ncbi/pgap.git Path: task_types/tt_extract_gencoll_ids.cwl Branch/Commit ID: f225cd99b0e0a5043dd102f8b33a6139fefe9ea4
	scatter-valuefrom-wf6.cwl	https://github.com/common-workflow-language/cwltool.git Path: cwltool/schemas/v1.0/v1.0/scatter-valuefrom-wf6.cwl Branch/Commit ID: 7bfe73a708dbf31d037303bb5a8fed1a79984b0f
	Running cellranger count and lineage inference	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e
	bgzip and index VCF	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/bgzip_and_index.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f
	advanced-header.cwl	https://github.com/datirium/workflows.git Path: metadata/advanced-header.cwl Branch/Commit ID: 10ce6e113f749c7bd725e426445220c3bdc5ddf1
	umi duplex alignment fastq workflow	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/alignment_umi_duplex.cwl Branch/Commit ID: 0b6e8fd8ead7644cf5398395b76af5cf4011686f
	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: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e
	cosifer-workflow.cwl	https://github.com/inab/ipc_workflows.git Path: cosifer/cwl/cosifer-workflow.cwl Branch/Commit ID: f0a821f8038717507ab6d8c7941e21b36969fa16
	alignment for mouse with qc	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/alignment_wgs_mouse.cwl Branch/Commit ID: 2979b565f88ceebca934611adbf3fb8cefd65a19
	wgs alignment and germline variant detection	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/germline_wgs_gvcf.cwl Branch/Commit ID: 0b6e8fd8ead7644cf5398395b76af5cf4011686f