Explore Workflows
View already parsed workflows here or click here to add your own
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HS Metrics workflow
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Path: definitions/subworkflows/hs_metrics.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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exome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_exome_mouse.cwl Branch/Commit ID: downsample_and_recall |
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bulk_analysis.cwl
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Path: steps/bulk_analysis.cwl Branch/Commit ID: 102d8cb |
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exome alignment with qc
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Path: definitions/pipelines/alignment_exome.cwl Branch/Commit ID: downsample_and_recall |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: low-vaf |
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download_check.cwl
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Path: genomel/cwl/workflows/utils/download_check.cwl Branch/Commit ID: master |
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md5-validate.cwl
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Path: cwl_awsem_v1/md5-validate.cwl Branch/Commit ID: dev2 |
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exomeseq-00-prepare-reference-data.cwl
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Path: subworkflows/exomeseq-00-prepare-reference-data.cwl Branch/Commit ID: master |
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wesp2.cwl
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Path: workflows/wesp2.cwl Branch/Commit ID: dev |
