Explore Workflows
View already parsed workflows here or click here to add your own
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iwdr_with_nested_dirs.cwl
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Path: v1.0/v1.0/iwdr_with_nested_dirs.cwl Branch/Commit ID: e67f19d8a713759d761ecad050966d1eb043b85c |
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running cellranger mkfastq and count
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Path: definitions/subworkflows/cellranger_mkfastq_and_count.cwl Branch/Commit ID: 509938802c5e42bb8084c6a5a26ab6425c60e69a |
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Tumor-Only Detect Variants workflow
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Path: definitions/pipelines/tumor_only_detect_variants.cwl Branch/Commit ID: 9c9e6a6a48eb321804ce772a2c2c12b4f2f32529 |
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tRNA_selection.cwl
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Path: tools/tRNA_selection.cwl Branch/Commit ID: c34db66a79cec3b66a0f1be5e499eef88db5a9ed |
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SoupX (workflow) - an R package for the estimation and removal of cell free mRNA contamination
Wrapped in a workflow SoupX tool for easy access to Cell Ranger pipeline compressed outputs. |
Path: tools/soupx-subworkflow.cwl Branch/Commit ID: 4360fb2e778ecee42e5f78f83b78c65ab3a2b1df |
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: c34db66a79cec3b66a0f1be5e499eef88db5a9ed |
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collate_unique_SSU_headers.cwl
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Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: c34db66a79cec3b66a0f1be5e499eef88db5a9ed |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 233f026ffce240071edda526391be0c03186fce8 |
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Unaligned BAM to BQSR and VCF
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Path: definitions/subworkflows/bam_to_bqsr_no_dup_marking.cwl Branch/Commit ID: f45b52a24c7b54a75368dcbab24b4eb2c5a9c75a |
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exome alignment and tumor-only variant detection
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Path: definitions/pipelines/tumor_only_exome.cwl Branch/Commit ID: 9e5f228bc1a3d0dfe950b5d41d7e4319e834a6d4 |
