Explore Workflows

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

Graph	Name	Retrieved From	View
	cluster_blastp_wnode and gpx_qdump combined	https://github.com/ncbi/pgap.git Path: task_types/tt_cluster_and_qdump.cwl Branch/Commit ID: e6fd7898b71a89b667d2eb38f412999920be5902
	WGS QC workflow	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/qc_wgs.cwl Branch/Commit ID: c711498c04d6b8ddf92ddceb6219f074765f7993
	bwa_pe.cwl	https://github.com/nci-gdc/gdc-dnaseq-cwl.git Path: workflows/bamfastq_align/bwa_pe.cwl Branch/Commit ID: 10c05314890db2b5bd85c3d338d7f5657fe0c646
	cluster_blastp_wnode and gpx_qdump combined	https://github.com/ncbi/pgap.git Path: task_types/tt_cluster_and_qdump.cwl Branch/Commit ID: 8a8fffb78b1e327ba0da51840ac8acc0c218d611
	merge and annotate svs with population allele freq and vep	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: c711498c04d6b8ddf92ddceb6219f074765f7993
	Exome QC workflow	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/qc_exome.cwl Branch/Commit ID: c711498c04d6b8ddf92ddceb6219f074765f7993
	exome alignment and germline variant detection	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: c711498c04d6b8ddf92ddceb6219f074765f7993
	SV filtering workflow	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/filter_sv_vcf.cwl Branch/Commit ID: c711498c04d6b8ddf92ddceb6219f074765f7993
	Subworkflow that runs cnvkit in single sample mode and returns a vcf file	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: c711498c04d6b8ddf92ddceb6219f074765f7993
	module-2	https://github.com/mskcc/roslin-variant.git Path: setup/cwl/module-2.cwl Branch/Commit ID: f1d57f1774b959979ed590c89e11f05b2c639d7c