Explore Workflows
View already parsed workflows here or click here to add your own
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EMG core analysis for Illumina
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Path: workflows/emg-core-analysis-v4.cwl Branch/Commit ID: 1b0851e |
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pipeline.cwl
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Path: pipeline.cwl Branch/Commit ID: c2c4f45 |
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wf_paleocar_web-app_data_flow.cwl
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Path: yw_cwl_modeling/yw_cwl_parser_old/Examples/main/wf_paleocar_web-app_data_flow.cwl Branch/Commit ID: master |
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Task2
For CMRxRecon validation |
Path: workflow-task2.cwl Branch/Commit ID: master |
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fillout_index_prefilter.cwl
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Path: cwl/fillout_index_prefilter.cwl Branch/Commit ID: master |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: No_filters_detect_variants |
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Per-chromosome pindel
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Path: pindel/pindel_cat.cwl Branch/Commit ID: master |
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ST520101.cwl
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Path: wf5201/ST520101.cwl Branch/Commit ID: main |
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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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gathered exome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_exome_gathered.cwl Branch/Commit ID: low-vaf |
