Explore Workflows
View already parsed workflows here or click here to add your own
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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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scatter_head.cwl
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Path: tests/cwl/scatter_head.cwl Branch/Commit ID: master |
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workflow.cwl
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Path: flow_create_genomics-workspace_yml/flow_create_yml/workflow.cwl Branch/Commit ID: master |
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count-lines11-extra-step-wf-noET.cwl
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Path: tests/count-lines11-extra-step-wf-noET.cwl Branch/Commit ID: main |
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count-lines3-wf.cwl
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Path: tests/count-lines3-wf.cwl Branch/Commit ID: main |
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exome alignment with qc
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Path: definitions/pipelines/alignment_exome.cwl Branch/Commit ID: master |
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no-inputs-wf.cwl
Workflow without inputs. |
Path: tests/no-inputs-wf.cwl Branch/Commit ID: main |
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WGS QC workflow
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Path: definitions/subworkflows/qc_wgs.cwl Branch/Commit ID: master |
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CODEX analysis pipeline using Cytokit
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Path: pipeline.cwl Branch/Commit ID: no-gpu-for-cwl-vis-only |
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ACCESS_pipeline.cwl
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Path: workflows/ACCESS_pipeline.cwl Branch/Commit ID: master |
