Explore Workflows
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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: master |
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pipeline.cwl
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![]() Path: pipeline.cwl Branch/Commit ID: 8c65f17 |
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Functional analyis of sequences that match the 16S SSU
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![]() Path: workflows/16S_taxonomic_analysis.cwl Branch/Commit ID: 135976d |
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STAR-RNA-Seq alignment and transcript/gene abundance workflow
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![]() Path: definitions/pipelines/rnaseq_star_fusion.cwl Branch/Commit ID: master |
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ST520107.cwl
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![]() Path: wf5201/ST520107.cwl Branch/Commit ID: main |
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Functional analyis of sequences that match the 16S SSU
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![]() Path: workflows/16S_functional_analysis.cwl Branch/Commit ID: caea457 |
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functional analysis prediction with InterProScan
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![]() Path: workflows/functional_analysis.cwl Branch/Commit ID: fa86fce |
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pipeline.cwl
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![]() Path: pipeline.cwl Branch/Commit ID: 0da4327 |
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count-lines1-wf.cwl
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![]() Path: tests/count-lines1-wf.cwl Branch/Commit ID: master |
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ST520106.cwl
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![]() Path: ST520106.cwl Branch/Commit ID: main |