Explore Workflows
View already parsed workflows here or click here to add your own
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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 |
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rnaseq_pipeline_fastq.cwl
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Path: topmed-workflows/TOPMed_RNAseq_pipeline/rnaseq_pipeline_fastq.cwl Branch/Commit ID: master |
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vecscreen_and_filter_workflow.cwl
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Path: progs/vecscreen_and_filter_workflow.cwl Branch/Commit ID: main |
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rna-seq-pipeline.cwl
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Path: gtex-rnaseq-pipeline/rna-seq-pipeline.cwl Branch/Commit ID: master |
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Transcriptome assembly workflow (paired-end version)
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Path: workflows/TranscriptomeAssembly-wf.paired-end.cwl Branch/Commit ID: assembly |
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cwlsite.cwl
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Path: site/cwlsite.cwl Branch/Commit ID: master |
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GATK-v1.0-Workflow.cwl
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Path: GATK-v1.0-Workflow.cwl Branch/Commit ID: master |
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strelkaSomaticVariantCaller_v0_1_1.cwl
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Path: janis_pipelines/wgs_somatic/cwl/tools/strelkaSomaticVariantCaller_v0_1_1.cwl Branch/Commit ID: master |
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dynresreq-workflow-tooldefault.cwl
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Path: tests/dynresreq-workflow-tooldefault.cwl Branch/Commit ID: master |
