Explore Workflows
View already parsed workflows here or click here to add your own
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conditional_step_no_inputs.cwl
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Path: tests/wf/conditional_step_no_inputs.cwl Branch/Commit ID: 190415a46a7249ab85fde87d797ec1ea688a8cc5 |
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mutect panel-of-normals workflow
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Path: definitions/pipelines/panel_of_normals.cwl Branch/Commit ID: No_filters_detect_variants |
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Complex DAG
Non-linear combination of KnowEnG tools |
Path: code/workflow.cwl Branch/Commit ID: master |
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spiel.cwl
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Path: spiel.cwl Branch/Commit ID: master |
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SSU-from-tablehits.cwl
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Path: tools/SSU-from-tablehits.cwl Branch/Commit ID: master |
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Find reads with predicted coding sequences above 60 AA in length
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Path: workflows/orf_prediction.cwl Branch/Commit ID: d4e5e53 |
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count-lines18-wf.cwl
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Path: tests/count-lines18-wf.cwl Branch/Commit ID: ea9f8634e41824ac3f81c3dde698d5f0eef54f1b |
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SSU-from-tablehits.cwl
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Path: tools/SSU-from-tablehits.cwl Branch/Commit ID: f993cad |
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EMG pipeline v4.0 (single end version)
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Path: workflows/emg-pipeline-v4-single.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. |
Path: samtoolsW.cwl Branch/Commit ID: release |
