Explore Workflows
View already parsed workflows here or click here to add your own
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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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wf_demultiplex_se.cwl
This workflow takes in single-end reads, and performs the following steps in order: demux_se.cwl (does not actually demux for single end, but mirrors the paired-end processing protocol) |
Path: cwl/wf_demultiplex_se.cwl Branch/Commit ID: master |
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wf-variantcall.cwl
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Path: somatic-lowfreq/pisces-titr-workflow/wf-variantcall.cwl Branch/Commit ID: master |
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canine_strelka2_module.cwl
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Path: subworkflows/canine_strelka2_module.cwl Branch/Commit ID: master |
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module-2.cwl
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Path: workflows/module-2.cwl Branch/Commit ID: 0.0.33_dmp |
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bulk_analysis.cwl
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Path: steps/bulk_analysis.cwl Branch/Commit ID: 44dbe38 |
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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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count-lines10-wf.cwl
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Path: tests/count-lines10-wf.cwl Branch/Commit ID: main |
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etl_http.cwl
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Path: workflows/dnaseq/etl_http.cwl Branch/Commit ID: 1.0 |
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scRNA-seq pipeline using Salmon and Alevin
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Path: pipeline.cwl Branch/Commit ID: cee6caf |
