Explore Workflows

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

Graph	Name	Retrieved From	View
	snaptools_create_snap_file.cwl	https://github.com/hubmapconsortium/sc-atac-seq-pipeline.git Path: steps/snaptools_create_snap_file.cwl Branch/Commit ID: bb023f9
	RNASelector as a CWL workflow https://doi.org/10.1007/s12275-011-1213-z	https://github.com/ProteinsWebTeam/ebi-metagenomics-cwl.git Path: workflows/rna-selector.cwl Branch/Commit ID: ca6ca61
	main.cwl	https://github.com/smc-rna-challenge/Ginny-9609498.git Path: main.cwl Branch/Commit ID: master
	ChIP-exo peak caller workflow for single-end samples This workflow execute peak caller and QC from ChIP-exo for single-end samples	https://gitlab.com/r78v10a07/cwl-workflow.git Path: workflows/ChIP-exo/peak_caller-SE.cwl Branch/Commit ID: master
	wrf_emep_full_workflow.cwl	https://github.com/UoMResearchIT/wrf_emep_cwl_linear_workflow.git Path: wrf_emep_full_workflow.cwl Branch/Commit ID: develop
	Salmon quantification, FASTQ -> H5AD count matrix	https://github.com/hubmapconsortium/multiome-rna-atac-pipeline.git Path: salmon-rnaseq/steps/salmon-quantification.cwl Branch/Commit ID: 999afe5
	exomeseq-02-variantdiscovery.cwl	https://github.com/Duke-GCB/bespin-cwl.git Path: subworkflows/exomeseq-02-variantdiscovery.cwl Branch/Commit ID: master
	Apply filters to VCF file	https://github.com/apaul7/cancer-genomics-workflow.git Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: low-vaf
	Tumor-Only Detect Variants workflow	https://github.com/genome/cancer-genomics-workflow.git Path: detect_variants/tumor_only_detect_variants.cwl Branch/Commit ID: toil_compatibility
	preprocess-illumina.cwl	https://github.com/fjrmoreews/cwl-workflow-SARS-CoV-2.git Path: PreProcessing/preprocess-illumina.cwl Branch/Commit ID: preprocessing