Explore Workflows
View already parsed workflows here or click here to add your own
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mut2.cwl
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Path: tests/wf/mut2.cwl Branch/Commit ID: 814bd0405a7701efc7d63e8f0179df394c7766f7 |
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env-wf2.cwl
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Path: cwltool/schemas/v1.0/v1.0/env-wf2.cwl Branch/Commit ID: 7bfd77118cdc80dd7150115dd7a1a7ee6046f6fe |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: aba52e94b6d7470132d3c092c26d67e29d615300 |
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Build STAR indices
Workflow runs [STAR](https://github.com/alexdobin/STAR) v2.5.3a (03/17/2017) PMID: [23104886](https://www.ncbi.nlm.nih.gov/pubmed/23104886) to build indices for reference genome provided in a single FASTA file as fasta_file input and GTF annotation file from annotation_gtf_file input. Generated indices are saved in a folder with the name that corresponds to the input genome. |
Path: workflows/star-index.cwl Branch/Commit ID: bf80c9339d81a78aefb8de661bff998ed86e836e |
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AcceptParameterFailure
validation or review of parameter updates failed. Action required and feedback to be provided. |
Path: workflows/AcceptParameterFailure.cwl Branch/Commit ID: 789752af87eb190387ff2acb4c95c7a5cdb961e7 |
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trim-rnaseq-pe.cwl
Runs RNA-Seq BioWardrobe basic analysis with pair-end data file. |
Path: workflows/trim-rnaseq-pe.cwl Branch/Commit ID: 812b0ff40dda18ab7a9a872ff13a577be8531ba6 |
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Quality assessment, amplicon classification and functional prediction
Workflow for quality assessment of paired reads and classification using NGTax 2.0 and functional annotation using picrust2. In addition files are exported to their respective subfolders for easier data management in a later stage. Steps: - FastQC (read quality control) - NGTax 2.0 - Picrust 2 - Export module for ngtax |
Path: cwl/workflows/workflow_ngtax_picrust2.cwl Branch/Commit ID: 2242521957bb07fc589d6bb07046f6a166bc975a |
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animal-genome-assembly.with_canu.cwl
Animal Genome Assembly pipeline by Kazuharu Arakawa (@gaou_ak), CWLized by Tazro Ohta (@inutano). This workflow contains assembly step by canu which may take a few weeks to complete. Be careful to run! |
Path: workflow/animal-genome-assembly/animal-genome-assembly.with_canu.cwl Branch/Commit ID: b63171820f546def8c26f558182912a71af88b48 |
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exomeseq-01-preprocessing.cwl
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Path: subworkflows/exomeseq-01-preprocessing.cwl Branch/Commit ID: 727ad5dbd15ef6aaa9cd5a3f7b23e74ff74663ea |
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bam-bedgraph-bigwig.cwl
Workflow converts input BAM file into bigWig and bedGraph files. Input BAM file should be sorted by coordinates (required by `bam_to_bedgraph` step). If `split` input is not provided use true by default. Default logic is implemented in `valueFrom` field of `split` input inside `bam_to_bedgraph` step to avoid possible bug in cwltool with setting default values for workflow inputs. `scale` has higher priority over the `mapped_reads_number`. The last one is used to calculate `-scale` parameter for `bedtools genomecov` (step `bam_to_bedgraph`) only in a case when input `scale` is not provided. All logic is implemented inside `bedtools-genomecov.cwl`. `bigwig_filename` defines the output name only for generated bigWig file. `bedgraph_filename` defines the output name for generated bedGraph file and can influence on generated bigWig filename in case when `bigwig_filename` is not provided. All workflow inputs and outputs don't have `format` field to avoid format incompatibility errors when workflow is used as subworkflow. |
Path: tools/bam-bedgraph-bigwig.cwl Branch/Commit ID: 94c6ea7bf4b64599746d778568efbd8e10f0d5ba |
