Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: downsample_and_recall |
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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: master |
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snaptools_create_snap_file.cwl
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Path: steps/snaptools_create_snap_file.cwl Branch/Commit ID: 302f1f3 |
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module-3.cwl
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Path: workflows/module-3.cwl Branch/Commit ID: master |
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Detect Variants workflow
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Path: definitions/pipelines/detect_variants.cwl Branch/Commit ID: downsample_and_recall |
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ST520113.cwl
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Path: wf5201/ST520113.cwl Branch/Commit ID: main |
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Bisulfite QC tools
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Path: definitions/subworkflows/bisulfite_qc.cwl Branch/Commit ID: low-vaf |
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pipeline_cavatica.cwl
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Path: pipeline_cavatica.cwl Branch/Commit ID: main |
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ST610106.cwl
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Path: ST610106.cwl Branch/Commit ID: remove-cycles |
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02-trim-pe.cwl
STARR-seq 02 trimming - reads: PE |
Path: v1.0/STARR-seq_pipeline/02-trim-pe.cwl Branch/Commit ID: master |
