Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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io-int-optional-wf.cwl
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![]() Path: v1.0/v1.0/io-int-optional-wf.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b |
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downsample unaligned BAM and align
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![]() Path: definitions/subworkflows/downsampled_alignment.cwl Branch/Commit ID: 2ae0a374fab650757cdae4391c8cbd32f02edf97 |
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exome alignment and germline variant detection
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![]() Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: 3042812447d9e8889c6118986490e9c9b9b13223 |
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output-arrays-file-wf.cwl
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![]() Path: v1.0/v1.0/output-arrays-file-wf.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b |
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chip-seq-alignment.cwl
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![]() Path: workflows/ChIP-Seq/chip-seq-alignment.cwl Branch/Commit ID: 3b9736a19eed3efc8f6cc587df282aad4f50a2ee |
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scatterfail.cwl
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![]() Path: tests/wf/scatterfail.cwl Branch/Commit ID: e4a52682f3bdefafe5c27e32983fed31116ac489 |
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Varscan Workflow
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![]() Path: definitions/subworkflows/varscan_pre_and_post_processing.cwl Branch/Commit ID: cfdcd0735e8fb1ac0b97f1a5cbe0cc7e00033dd0 |
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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: 742dbafb5fb103d8578f48a0576c14dd8dae3b2a |
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genomel_cohort_gatk4.cwl
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![]() Path: genomel/genomel_cohort_gatk4.cwl Branch/Commit ID: 28bb82ba031041321ff9caa5c299ec1bb15d7471 |
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import_schema-def.cwl
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![]() Path: v1.0/v1.0/import_schema-def.cwl Branch/Commit ID: ca8e6661b5cab1f017e5bc4024650722dae4d50b |