Explore Workflows
View already parsed workflows here or click here to add your own
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: downsample_and_recall |
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wgs alignment with qc
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Path: definitions/pipelines/alignment_wgs.cwl Branch/Commit ID: downsample_and_recall |
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Detect Variants workflow for WGS pipeline
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Path: definitions/pipelines/detect_variants_wgs.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: downsample_and_recall |
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Chipseq alignment with qc and creating homer tag directory
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Path: definitions/pipelines/chipseq.cwl Branch/Commit ID: downsample_and_recall |
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alignment for mouse with qc
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Path: definitions/pipelines/alignment_wgs_mouse.cwl Branch/Commit ID: downsample_and_recall |
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Immunotherapy Workflow
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Path: definitions/pipelines/immuno.cwl Branch/Commit ID: downsample_and_recall |
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exome alignment and germline variant detection
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Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: downsample_and_recall |
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03-map-se-blacklist-removal.cwl
ATAC-seq 03 mapping - reads: SE |
Path: v1.0/ATAC-seq_pipeline/03-map-se-blacklist-removal.cwl Branch/Commit ID: v1.0 |
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picard_markduplicates
Mark duplicates |
Path: structuralvariants/cwl/abstract_operations/subworkflows/picard_markduplicates.cwl Branch/Commit ID: master |
