Explore Workflows
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Graph | Name | Retrieved From | View |
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tt_hmmsearch_wnode.cwl
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![]() Path: task_types/tt_hmmsearch_wnode.cwl Branch/Commit ID: 42712bca4c3307d87b6b55f525a4c97cb6f7e288 |
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hmmsearch_wnode and gpx_qdump combined workflow to apply scatter/gather
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![]() Path: task_types/tt_hmmsearch_wnode_plus_qdump.cwl Branch/Commit ID: f5d70f3ad365a2c017fab1c9654c88bc1caf41aa |
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js_output_workflow.cwl
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![]() Path: tests/wf/js_output_workflow.cwl Branch/Commit ID: 75271e2a0887d47cca4077b60dd51ac763c09b63 |
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CreateSymlink-workflow.cwl
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![]() Path: CreateSymlink-workflow.cwl Branch/Commit ID: 58b23bf2d10154a5f2296df8fce496de4cecffef |
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fail-unconnected.cwl
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![]() Path: v1.0/v1.0/fail-unconnected.cwl Branch/Commit ID: 148f11b11d31c098196e649f680797f0b4680114 |
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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. |
![]() Path: samtoolsW.cwl Branch/Commit ID: fcab170f3e8a4bc70601650401cce2a9df42f484 |
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hmmsearch_wnode and gpx_qdump combined workflow to apply scatter/gather
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![]() Path: task_types/tt_hmmsearch_wnode_plus_qdump.cwl Branch/Commit ID: 42712bca4c3307d87b6b55f525a4c97cb6f7e288 |
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functional-wf.cwl
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![]() Path: tests/checker_wf/functional-wf.cwl Branch/Commit ID: 520acbfb82455c4bdabd5f2ea24842804e1c9f58 |
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cluster_blastp_wnode and gpx_qdump combined
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![]() Path: task_types/tt_cluster_and_qdump.cwl Branch/Commit ID: f5d70f3ad365a2c017fab1c9654c88bc1caf41aa |
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search.cwl#main
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![]() Path: cwltool/schemas/v1.0/v1.0/search.cwl Branch/Commit ID: 814bd0405a7701efc7d63e8f0179df394c7766f7 Packed ID: main |