Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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exome alignment and germline variant detection
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![]() Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: c625e05eefb1754353c1bdfa46c01dc61e6233dd |
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split_bam_subpipeline.cwl
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![]() Path: janis_pipelines/wgs_somatic/cwl/tools/split_bam_subpipeline.cwl Branch/Commit ID: db347697cbf46ed1d160d50666943bd56a2646f4 |
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assm_assm_blastn_wnode
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![]() Path: task_types/tt_assm_assm_blastn_wnode.cwl Branch/Commit ID: 47ccbd0bc7b45bf8b3c92d0a66c1a9a232367a5d |
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Detect Variants workflow
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![]() Path: definitions/pipelines/detect_variants_mouse.cwl Branch/Commit ID: eb0092603bf57acb7bda08a06e4f2f1e2a8c9b6d |
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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: 06d2440d115b446c299b4ce96e8812d2f8df86ec |
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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: 06d2440d115b446c299b4ce96e8812d2f8df86ec |
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exome alignment and germline variant detection
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![]() Path: definitions/pipelines/germline_exome.cwl Branch/Commit ID: bed420556091b7b8b45cf20a95e5947e1de9a416 |
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vecscreen.cwl
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![]() Path: vecscreen/vecscreen.cwl Branch/Commit ID: 48381989cb983567ed936fde632714933df65350 |
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bacterial_screening.cwl
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![]() Path: vecscreen/bacterial_screening.cwl Branch/Commit ID: 02816f0d66e36c8eeba02d211cc90e36bf1c9df5 |
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tt_fscr_calls_pass1
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![]() Path: task_types/tt_fscr_calls_pass1.cwl Branch/Commit ID: 02816f0d66e36c8eeba02d211cc90e36bf1c9df5 |