Explore Workflows
View already parsed workflows here or click here to add your own
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trim-rnaseq-se.cwl
Runs RNA-Seq BioWardrobe basic analysis with single-end data file. |
Path: workflows/trim-rnaseq-se.cwl Branch/Commit ID: b4b7b2e7e508be5eac639f9e323d141daf714c0d |
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somatic_subpipeline.cwl
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Path: janis_pipelines/wgs_somatic/cwl/tools/somatic_subpipeline.cwl Branch/Commit ID: f7f887b84734a932534ed6a4732a48852e6169d4 |
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umi duplex alignment workflow
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Path: definitions/subworkflows/duplex_alignment.cwl Branch/Commit ID: 051074fce4afd9732ef34db9dd43d3a1d8e979d6 |
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wf-loadContents4.cwl
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Path: tests/wf-loadContents4.cwl Branch/Commit ID: e62f99dd79d6cb9c157cceb458f74200da84f6e9 |
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GATKBaseRecalBQSRWorkflow_4_1_3.cwl
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Path: janis_pipelines/wgs_somatic/cwl/tools/GATKBaseRecalBQSRWorkflow_4_1_3.cwl Branch/Commit ID: f7f887b84734a932534ed6a4732a48852e6169d4 |
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no-outputs-wf.cwl
Workflow without outputs. |
Path: tests/no-outputs-wf.cwl Branch/Commit ID: ea9f8634e41824ac3f81c3dde698d5f0eef54f1b |
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Build Bowtie indices
Workflow runs [Bowtie](http://bowtie-bio.sourceforge.net/tutorial.shtml) v1.2.0 (12/30/2016) to build indices for reference genome provided in a single FASTA file as fasta_file input. Generated indices are saved in a folder with the name that corresponds to the input genome |
Path: workflows/bowtie-index.cwl Branch/Commit ID: 7eef0294395d83ff0765fce61726a59d71126422 |
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scatter-wf1_v1_2.cwl
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Path: testdata/scatter-wf1_v1_2.cwl Branch/Commit ID: 0ad6983898f0d9001fe0f416f97c4d8b940e384a |
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CLIP-Seq pipeline for single-read experiment NNNNG
CLIP-Seq workflow for single-read experiment. |
Path: workflows/clipseq-se.cwl Branch/Commit ID: cb5e5b8563be4977e9f2babc14fe084faa234847 |
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genome-kallisto-index.cwl
Generates a FASTA file with the DNA sequences for all transcripts in a GFF file and builds kallisto index |
Path: tools/genome-kallisto-index.cwl Branch/Commit ID: a8909e86f5bcb048d136f9a7d70b4b6f8f4e485f |
