Explore Workflows

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

Graph	Name	Retrieved From	View
	mixed_library_metrics.cwl	https://github.com/NCI-GDC/gdc-dnaseq-cwl.git Path: workflows/mirnaseq/mixed_library_metrics.cwl Branch/Commit ID: a57b8f0d8708078e87f13297e065d72db10e38a0
	nestedworkflows.cwl	https://github.com/common-workflow-language/common-workflow-language.git Path: v1.0/examples/nestedworkflows.cwl Branch/Commit ID: 622134ebc48980676b7e53fe39405c428920c03e
	protein_extract	https://github.com/ncbi-gpipe/pgap.git Path: progs/protein_extract.cwl Branch/Commit ID: 71e3a42eadc007b66ef4689086530dfc3123d32f
	snpeff-workflow.cwl Annotate variants provided in a gziped VCF using SnpEff	https://github.com/andrewjesaitis/cwl-tutorial.git Path: snpeff-workflow.cwl Branch/Commit ID: 9c8de191477ca98f6b4088cf010e973a3c3811b9
	metrics.cwl	https://github.com/NCI-GDC/gdc-dnaseq-cwl.git Path: workflows/dnaseq/metrics.cwl Branch/Commit ID: 14558b578bad217685ae3c4807ead2a4392d0319
	count-lines3-wf.cwl	https://github.com/common-workflow-language/common-workflow-language.git Path: v1.0/v1.0/count-lines3-wf.cwl Branch/Commit ID: 8dbb46740ea700469b609ae9a05f13e95cb5af6a
	hmmsearch_wnode and gpx_qdump combined workflow to apply scatter/gather	https://github.com/ncbi/pgap.git Path: task_types/tt_hmmsearch_wnode_plus_qdump.cwl Branch/Commit ID: 13b411d94a568e52797ba936732dc65f1a91bd41
	extract_readgroup_fastq_se.cwl	https://github.com/nci-gdc/gdc-dnaseq-cwl.git Path: workflows/bamfastq_align/extract_readgroup_fastq_se.cwl Branch/Commit ID: cf2e9d7c3cc87ce97a1fbf73fad574b170fedcfb
	extract_gencoll_ids	https://github.com/ncbi-gpipe/pgap.git Path: task_types/tt_extract_gencoll_ids.cwl Branch/Commit ID: 41dfc42a730087189122a2f74b2f547a4665a225
	exome alignment and germline variant detection	https://github.com/genome/cancer-genomics-workflow.git Path: germline_exome_workflow.cwl Branch/Commit ID: ab3cc1f460146c60d7de417508f0c1ea70506e6a