Explore Workflows
View already parsed workflows here or click here to add your own
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Whole genome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a |
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workflow.cwl
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Path: flow_md5checksums/workflow.cwl Branch/Commit ID: 0b58c250e8ab7c5efae29443f08ea74316127041 |
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Cell Ranger Count Gene Expression
Cell Ranger Count Gene Expression ================================= |
Path: workflows/single-cell-preprocess-cellranger.cwl Branch/Commit ID: b1a5dabeeeb9079b30b2871edd9c9034a1e00c1c |
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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: 336f7d1af649f42543baa6be2594cd872919b5b5 |
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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: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a |
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Detect DoCM variants
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Path: definitions/subworkflows/docm_germline.cwl Branch/Commit ID: 336f7d1af649f42543baa6be2594cd872919b5b5 |
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genomics-workspace.cwl
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Path: flow_genomicsWorkspace/genomics-workspace.cwl Branch/Commit ID: 0b58c250e8ab7c5efae29443f08ea74316127041 |
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FastQC - a quality control tool for high throughput sequence data
FastQC - a quality control tool for high throughput sequence data ===================================== FastQC aims to provide a simple way to do some quality control checks on raw sequence data coming from high throughput sequencing pipelines. It provides a modular set of analyses which you can use to give a quick impression of whether your data has any problems of which you should be aware before doing any further analysis. The main functions of FastQC are: - Import of data from FastQ files (any variant) - Providing a quick overview to tell you in which areas there may be problems - Summary graphs and tables to quickly assess your data - Export of results to an HTML based permanent report - Offline operation to allow automated generation of reports without running the interactive application |
Path: workflows/fastqc.cwl Branch/Commit ID: 09267e79fd867aa68a219c69e6db7d8e2e877be2 |
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adapter for sequence_align_and_tag
Some workflow engines won't stage files in our nested structure, so parse it out here |
Path: definitions/subworkflows/sequence_align_and_tag_adapter.cwl Branch/Commit ID: 336f7d1af649f42543baa6be2594cd872919b5b5 |
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workflow.cwl
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Path: flow_create_genomics-workspace_yml/flow_create_yml/workflow.cwl Branch/Commit ID: 0b58c250e8ab7c5efae29443f08ea74316127041 |
