Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
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gpas_gatk4.2.4.1_mutect2_tumor_only_workflow.cwl
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Path: gatk4-mutect2-tumor-only-cwl/gpas_gatk4.2.4.1_mutect2_tumor_only_workflow.cwl Branch/Commit ID: master |
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wf_vecscreen.cwl
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Path: contam_filter/wf_vecscreen.cwl Branch/Commit ID: master |
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sac-preprocess.cwl#align-texts-wf.cwl
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Path: ochre/cwl/sac-preprocess.cwl Branch/Commit ID: master Packed ID: align-texts-wf.cwl |
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mergeAndMarkBams_4_1_3.cwl
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Path: janis_pipelines/wgs_somatic/cwl/tools/mergeAndMarkBams_4_1_3.cwl Branch/Commit ID: master |
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chksum_for_corrupted_files.cwl
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Path: cwls/chksum_for_corrupted_files.cwl Branch/Commit ID: 0.5.0_test |
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clean_reads_qc.cwl
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Path: python/lib/MICGENT/data/cwl/clean_reads_qc.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: master |
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Detect DoCM variants
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Path: definitions/subworkflows/docm_germline.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 |
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kallisto_wf_pe.cwl
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Path: workflows/kallisto/paired_end/kallisto_wf_pe.cwl Branch/Commit ID: master |
