Explore Workflows
View already parsed workflows here or click here to add your own
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wgs alignment and germline variant detection
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![]() Path: definitions/pipelines/germline_wgs_gvcf.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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exome alignment and somatic variant detection
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![]() Path: definitions/pipelines/somatic_exome_nonhuman.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a |
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Nanopore assembly workflow
**Workflow for sequencing with ONT Nanopore data, from basecalled reads to (meta)assembly and binning**<br> - Workflow Nanopore Quality - Kraken2 taxonomic classification of FASTQ reads - Flye (de-novo assembly) - Medaka (assembly polishing) - metaQUAST (assembly quality reports) **When Illumina reads are provided:** - Workflow Illumina Quality: https://workflowhub.eu/workflows/336?version=1 - Assembly polishing with Pilon<br> - Workflow binnning https://workflowhub.eu/workflows/64?version=11 - Metabat2 - CheckM - BUSCO - GTDB-Tk **All tool CWL files and other workflows can be found here:**<br> Tools: https://git.wur.nl/unlock/cwl/-/tree/master/cwl<br> Workflows: https://git.wur.nl/unlock/cwl/-/tree/master/cwl/workflows<br> The dependencies are either accessible from https://unlock-icat.irods.surfsara.nl (anonymous,anonymous)<br> and/or<br> By using the conda / pip environments as shown in https://git.wur.nl/unlock/docker/-/blob/master/kubernetes/scripts/setup.sh<br> |
![]() Path: cwl/workflows/workflow_nanopore_assembly.cwl Branch/Commit ID: 2242521957bb07fc589d6bb07046f6a166bc975a |
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Chipseq alignment with qc and creating homer tag directory
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![]() Path: definitions/pipelines/chipseq.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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wgs alignment and tumor-only variant detection
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![]() Path: definitions/pipelines/tumor_only_wgs.cwl Branch/Commit ID: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e |
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Immunotherapy Workflow
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![]() Path: definitions/pipelines/immuno.cwl Branch/Commit ID: 9cbf2a483e1b9e4cdb8e2564be27a9e64fc1169e |
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exome alignment and tumor-only variant detection
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![]() Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 1750cd5cc653f058f521b6195e3bec1e7df1a086 |
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exome alignment and germline variant detection
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![]() Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: a59a803e1809a8fbfabca6b8962a8ad66dd01f1d |
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ROSE: rank ordering of super-enhancers
Super-enhancers, consist of clusters of enhancers that are densely occupied by the master regulators and Mediator. Super-enhancers differ from typical enhancers in size, transcription factor density and content, ability to activate transcription, and sensitivity to perturbation. Use to create stitched enhancers, and to separate super-enhancers from typical enhancers using sequencing data (.bam) given a file of previously identified constituent enhancers (.gff) |
![]() Path: workflows/super-enhancer.cwl Branch/Commit ID: c9e7f3de7f6ba38ee663bd3f9649e8d7dbac0c86 |
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Bisulfite alignment and QC
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![]() Path: definitions/pipelines/bisulfite.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a |