Explore Workflows
View already parsed workflows here or click here to add your own
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wf_calculate_models2.cwl
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Path: yw_cwl_modeling/calculate_models/wf_calculate_models2.cwl Branch/Commit ID: master |
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Functional analyis of sequences that match the 16S SSU
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Path: workflows/16S_taxonomic_analysis.cwl Branch/Commit ID: c1f8b22 |
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schemadef-wf.cwl
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Path: tests/schemadef-wf.cwl Branch/Commit ID: master |
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birds.cwl
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Path: birds.cwl Branch/Commit ID: visualise |
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standard_bam_to_collapsed_qc.cwl
This is a workflow to go from standard bams to collapsed bams and QC results. |
Path: workflows/subworkflows/standard_bam_to_collapsed_qc.cwl Branch/Commit ID: master |
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exome alignment and germline variant detection
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Path: definitions/subworkflows/germline_detect_variants.cwl Branch/Commit ID: master |
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umi duplex alignment workflow
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Path: definitions/subworkflows/duplex_alignment.cwl Branch/Commit ID: No_filters_detect_variants |
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SPRM pipeline
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Path: pipeline.cwl Branch/Commit ID: 62d3a80 |
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Prepare user input
Prepare user input for NCBI-PGAP pipeline |
Path: prepare_user_input2.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: low-vaf |
