Explore Workflows
View already parsed workflows here or click here to add your own
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gathered exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle_gathered.cwl Branch/Commit ID: f77a920bcc73f6cfdb091eed75a149d02cd8a263 |
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format_rrnas_from_seq_entry
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Path: task_types/tt_format_rrnas_from_seq_entry.cwl Branch/Commit ID: f5a467a21b8f69aef5666fb7bbf35efd98c0cbea |
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three_step_color.cwl
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Path: tests/wf/three_step_color.cwl Branch/Commit ID: d3c7bd5d6c409e857b98f9034a55952ca95afdb3 |
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cond-wf-007_nojs.cwl
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Path: tests/conditionals/cond-wf-007_nojs.cwl Branch/Commit ID: 31ec48a8d81ef7c1b2c5e9c0a19e7623efe4a1e2 |
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FASTQ to BQSR
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Path: definitions/subworkflows/fastq_to_bqsr.cwl Branch/Commit ID: 7f9dfad8e45ca096ae738cff646195b2b1ba7d7f |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf.cwl Branch/Commit ID: e7e888df9e7d44f036c4c7985e474016ee9e6525 |
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scatter-wf2.cwl
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Path: cwltool/schemas/v1.0/v1.0/scatter-wf2.cwl Branch/Commit ID: 49cd284a8fc7884de763573075d3e1d6a4c1ffdd |
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Single-Cell RNA-Seq Filtering Analysis
Single-Cell RNA-Seq Filtering Analysis Removes low-quality cells from the outputs of the “Cell Ranger Count (RNA)”, “Cell Ranger Count (RNA+VDJ)”, and “Cell Ranger Aggregate (RNA, RNA+VDJ)” pipelines. The results of this workflow are used in the “Single-Cell RNA-Seq Dimensionality Reduction Analysis” pipeline. |
Path: workflows/sc-rna-filter.cwl Branch/Commit ID: b4d578c2ba4713a5a22163d9f8c7105acda1f22e |
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scatterfail.cwl
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Path: tests/wf/scatterfail.cwl Branch/Commit ID: 6300a49ec29be956ab451311fe9781522f461aee |
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: a7838a5ca72b25db5c2af20a15f34303a839980e |
