Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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rw-distr.cwl
run scatter-gather for rw stage |
![]() Path: stage/rw-distr.cwl Branch/Commit ID: master |
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WGS QC workflow
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![]() Path: definitions/subworkflows/qc_wgs.cwl Branch/Commit ID: low-vaf |
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: downsample_and_recall |
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workflowSegmentTest.cwl
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![]() Path: saber/i2g/examples/I2G_Seg_Workflow/workflowSegmentTest.cwl Branch/Commit ID: master |
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wgs alignment with qc
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![]() Path: definitions/pipelines/alignment_wgs.cwl Branch/Commit ID: master |
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mutect parallel workflow
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![]() Path: definitions/subworkflows/mutect.cwl Branch/Commit ID: low-vaf |
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scRNA-seq pipeline using Salmon and Alevin
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![]() Path: pipeline.cwl Branch/Commit ID: ada7831 |
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read_preprocessing.cwl
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![]() Path: workflows/read_preprocessing.cwl Branch/Commit ID: master |
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somatic_exome: exome alignment and somatic variant detection
somatic_exome is designed to perform processing of mutant/wildtype H.sapiens exome sequencing data. It features BQSR corrected alignments, 4 caller variant detection, and vep style annotations. Structural variants are detected via manta and cnvkit. In addition QC metrics are run, including somalier concordance metrics. example input file = analysis_workflows/example_data/somatic_exome.yaml |
![]() Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: downsample_and_recall |
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io-int-default-tool-and-wf.cwl
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![]() Path: tests/io-int-default-tool-and-wf.cwl Branch/Commit ID: main |