Explore Workflows
View already parsed workflows here or click here to add your own
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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: a0b22644ca178b640fb74849d23b7c631022f0b5 |
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scatterfail.cwl
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Path: tests/wf/scatterfail.cwl Branch/Commit ID: 7dec97bb8f0bc2d9e9eb710faf41f2e98cc7cdda |
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Nested workflow example
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Path: tests/wf/nested.cwl Branch/Commit ID: e6a1e1f3a3b3168028bd19aaf465826fa276a35b |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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Nested workflow example
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Path: tests/wf/nested.cwl Branch/Commit ID: 7dec97bb8f0bc2d9e9eb710faf41f2e98cc7cdda |
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wffail.cwl
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Path: tests/wf/wffail.cwl Branch/Commit ID: 7dec97bb8f0bc2d9e9eb710faf41f2e98cc7cdda |
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Varscan Workflow
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Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: 195b4ab487c939eb32a55d9f78bc1befd100caae |
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MEME motif
This workflow uses MEME suite for motif finding |
Path: workflows/ChIP-Seq/meme-motif.cwl Branch/Commit ID: 3247592a89deafaa0d9c5910a1cb1d000ef9b098 |
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revsort.cwl
Reverse the lines in a document, then sort those lines. |
Path: tests/wf/revsort.cwl Branch/Commit ID: 7dec97bb8f0bc2d9e9eb710faf41f2e98cc7cdda |
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exome alignment and germline variant detection, with optitype for HLA typing
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Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
