Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
qiime2 demux sequences
Demultiplexing sequences from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
Path: packed/qiime2-step1-import-demux.cwl Branch/Commit ID: qiime2-workflow Packed ID: qiime2-02-demux.cwl |
|
|
|
hi-c-processing-pairs.cwl
|
Path: cwl_awsem_v1/hi-c-processing-pairs.cwl Branch/Commit ID: dev2 |
|
|
|
Immunotherapy Workflow
|
Path: definitions/pipelines/immuno.cwl Branch/Commit ID: master |
|
|
|
scRNA-seq pipeline using Salmon and Alevin
|
Path: pipeline.cwl Branch/Commit ID: 16dd8ca |
|
|
|
Subworkflow that runs cnvkit in single sample mode and returns a vcf file
|
Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: master |
|
|
|
rnaediting1strand.cwl
|
Path: CWL-SINGULARITY-pipeline-building-code/cwl/rnaediting1strand.cwl Branch/Commit ID: 6f21086 |
|
|
|
revsort.cwl
Reverse the lines in a document, then sort those lines. |
Path: tests/data/revsort-run-1/snapshot/revsort.cwl Branch/Commit ID: main |
|
|
|
Transcriptome assembly workflow (single-end version)
|
Path: workflows/TranscriptomeAssembly-wf.single-end.cwl Branch/Commit ID: assembly |
|
|
|
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: downsample_and_recall |
|
|
|
ConcordanceCheckerWorkflow.cwl
|
Path: vcf-comparator/ConcordanceCheckerWorkflow.cwl Branch/Commit ID: 1.30.0 |
