Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
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scatter-wf1.cwl
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https://github.com/common-workflow-language/cwl-v1.1.git
Path: tests/scatter-wf1.cwl Branch/Commit ID: master |
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beagle-imputation-per-region.cwl
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https://github.com/hacchy1983/imputation-server-jp.git
Path: Workflows/beagle-imputation-per-region.cwl Branch/Commit ID: main |
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any-type-compat.cwl
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https://github.com/common-workflow-language/common-workflow-language.git
Path: v1.0/v1.0/any-type-compat.cwl Branch/Commit ID: master |
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main.cwl
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https://github.com/CLAIRE-COVID/AI-Covid19-pipelines.git
Path: online/streamflow/cwl/main.cwl Branch/Commit ID: master |
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exome alignment and germline variant detection
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https://github.com/litd/analysis-workflows.git
Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: master |
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Complex DAG
Non-linear combination of KnowEnG tools |
https://github.com/KnowEnG-Research/cwl-specification.git
Path: code/workflow.cwl Branch/Commit ID: master |
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samtoolsW.cwl
Author: AMBARISH KUMAR er.ambarish@gmail.com; ambari73_sit@jnu.ac.in This is a proposed standard operating procedure for genomic variant detection using VARSCAN. It is hoped to be effective and useful for getting SARS-CoV-2 genome variants. It uses Illumina RNASEQ reads and genome sequence. |
https://github.com/ambarishK/bio-cwl-tools.git
Path: samtoolsW.cwl Branch/Commit ID: release |
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wf-loadContents4.cwl
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https://github.com/common-workflow-language/cwl-v1.2.git
Path: tests/wf-loadContents4.cwl Branch/Commit ID: main |
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cond-wf-011_nojs.cwl
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https://github.com/common-workflow-language/cwl-v1.2.git
Path: tests/conditionals/cond-wf-011_nojs.cwl Branch/Commit ID: main |
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rnaseq-star-rsem-deseq2.cwl
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https://github.com/pitagora-network/dat2-cwl.git
Path: workflow/rna-seq/rnaseq-star-rsem-deseq2/rnaseq-star-rsem-deseq2.cwl Branch/Commit ID: main |
