Explore Workflows
View already parsed workflows here or click here to add your own
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trnascan_wnode and gpx_qdump combined
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Path: bacterial_trna/wf_scan_and_dump.cwl Branch/Commit ID: 22ffe27d9d4a899def7592d75d5871c1856adbdb |
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allele-process-reference.cwl
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Path: subworkflows/allele-process-reference.cwl Branch/Commit ID: c602e3cdd72ff904dd54d46ba2b5146eb1c57022 |
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cond-wf-004.cwl
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Path: tests/conditionals/cond-wf-004.cwl Branch/Commit ID: 707ebcd2173889604459c5f4ffb55173c508abb3 |
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count-lines7-single-source-wf_v1_1.cwl
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Path: testdata/count-lines7-single-source-wf_v1_1.cwl Branch/Commit ID: 77669d4dd1d1ebd2bdd9810f911608146d9b8e51 |
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umi duplex alignment workflow
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Path: definitions/subworkflows/duplex_alignment.cwl Branch/Commit ID: ae75b938e6e8ae777a55686bbacad824b3c6788c |
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scatter-valuefrom-wf3.cwl#main
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Path: tests/scatter-valuefrom-wf3.cwl Branch/Commit ID: 707ebcd2173889604459c5f4ffb55173c508abb3 Packed ID: main |
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SetParameter
Receive, assert, and validate new simulation model parameters. Update simulation model data base after passing all outlined steps. |
Path: workflows/SetParameter.cwl Branch/Commit ID: 84b99c6e475ad104cdd714d8588ff49805763420 |
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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: 27dcb1ae121be6a23057b74332b8c752ea425735 |
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count-lines1-wf.cwl
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Path: cwltool/schemas/v1.0/v1.0/count-lines1-wf.cwl Branch/Commit ID: 526f36f93655bfb098f766ff020708b5a707513a |
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Single-Cell RNA-Seq Cluster Analysis
Single-Cell RNA-Seq Cluster Analysis Clusters cells by similarity of gene expression data from the outputs of the “Single-Cell RNA-Seq Dimensionality Reduction Analysis” pipeline. The results of this workflow are used in the “Single-Cell Manual Cell Type Assignment”, “Single-Cell RNA-Seq Differential Expression Analysis”, “Single-Cell RNA-Seq Trajectory Analysis”, and “Single-Cell Differential Abundance Analysis” pipelines. |
Path: workflows/sc-rna-cluster.cwl Branch/Commit ID: 261c0232a7a40880f2480b811ed2d7e89c463869 |
