Explore Workflows

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

Graph	Name	Retrieved From	View
	Detect Variants workflow for WGS pipeline	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/detect_variants_wgs.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a
	wf_bam_to_bigwig.cwl	https://github.com/YeoLab/sailor.git Path: cwl/wf_bam_to_bigwig.cwl Branch/Commit ID: 5eb7864dd3622552dc95a927d3eb6ccf5f107745
	bams2gvcf.wBQSR.cwl	https://github.com/ddbj/human-reseq.git Path: Workflows/bams2gvcf.wBQSR.cwl Branch/Commit ID: 4c49df49844f3e82b8fc4f30a3809ac6dc4f299a
	scatter-valuefrom-inputs-wf1.cwl	https://github.com/common-workflow-language/common-workflow-language.git Path: v1.0/v1.0/scatter-valuefrom-inputs-wf1.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b
	vecscreen.cwl	https://github.com/ncbi/pgap.git Path: vecscreen/vecscreen.cwl Branch/Commit ID: a33936cca222084cf68e00076255359688b6708a
	birds.cwl	https://github.com/eosc-lofar/presto-cwl.git Path: birds.cwl Branch/Commit ID: f6661b12c4c28184e826e5e64113e6f04eb8e39c
	Filter single sample sv vcf from depth callers(cnvkit/cnvnator)	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: cfdcd0735e8fb1ac0b97f1a5cbe0cc7e00033dd0
	Data2Services CWL workflow to convert CSV/TSV files with statements split, Vincent Emonet <vincent.emonet@gmail.com>	https://github.com/MaastrichtU-IDS/bio2rdf.git Path: support/pharmgkb/graphdb-workflow/workflow.cwl Branch/Commit ID: 7b8487b8333da4773f3790414b0863fe48d1fb0f
	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