Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
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sum-wf-noET.cwl
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Path: tests/sum-wf-noET.cwl Branch/Commit ID: main |
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tRNA_selection.cwl
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Path: tools/tRNA_selection.cwl Branch/Commit ID: ef3c7b2 |
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wf_step3.cwl
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Path: yw_cwl_modeling/additional_test_cases/wf_step3.cwl Branch/Commit ID: master |
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wf_paleocar_web-app_data_flow.cwl
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Path: yw_cwl_modeling/yw_cwl_parser_old/Examples/main/wf_paleocar_web-app_data_flow.cwl Branch/Commit ID: master |
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bqsr-distr.cwl
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Path: stage/bqsr-distr.cwl Branch/Commit ID: master |
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: 71d9c83 |
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cnv_manta
CNV Manta calling |
Path: structuralvariants/cwl/subworkflows/cnv_manta.cwl Branch/Commit ID: 1.0.6 |
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any-type-compat.cwl
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Path: tests/any-type-compat.cwl Branch/Commit ID: main |
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image_series.cwl
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Path: utils/IM/LINC/lincSun/workflow/image_series.cwl Branch/Commit ID: master |
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biowardrobe_chipseq_se.cwl
The workflow is used to run CHIP-Seq basic analysis with single-end input FASTQ file. In outputs it returns coordinate sorted BAM file alongside with index BAI file, quality statistics of the input FASTQ file, reads coverage in a form of bigWig file, peaks calling data in a form of narrowPeak or broadPeak files. |
Path: biowardrobe_chipseq_se.cwl Branch/Commit ID: v0.0.5 |
