Explore Workflows
View already parsed workflows here or click here to add your own
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WGS QC workflow
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Path: definitions/subworkflows/qc_wgs.cwl Branch/Commit ID: 8cee1920920ed73384fb3ab74272da9c92a20cf2 |
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Generate ATDP heatmap using Homer
Generate ATDP heatmap centered on TSS from an array of input BAM files and genelist TSV file. Returns array of heatmap JSON files with the names that have the same basenames as input BAM files, but with .json extension |
Path: workflows/heatmap.cwl Branch/Commit ID: 730b40bc403263b724399a952c0f3e2d28f13519 |
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io-int-wf.cwl
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Path: tests/io-int-wf.cwl Branch/Commit ID: 664835e83eb5e57eee18a04ce7b05fb9d70d77b7 |
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DiffBind Multi-factor Analysis
DiffBind Multi-factor Analysis ------------------------------ DiffBind processes ChIP-Seq data enriched for genomic loci where specific protein/DNA binding occurs, including peak sets identified by ChIP-Seq peak callers and aligned sequence read datasets. It is designed to work with multiple peak sets simultaneously, representing different ChIP experiments (antibodies, transcription factor and/or histone marks, experimental conditions, replicates) as well as managing the results of multiple peak callers. For more information please refer to: ------------------------------------- Ross-Innes CS, Stark R, Teschendorff AE, Holmes KA, Ali HR, Dunning MJ, Brown GD, Gojis O, Ellis IO, Green AR, Ali S, Chin S, Palmieri C, Caldas C, Carroll JS (2012). “Differential oestrogen receptor binding is associated with clinical outcome in breast cancer.” Nature, 481, -4. |
Path: workflows/diffbind-multi-factor.cwl Branch/Commit ID: 261c0232a7a40880f2480b811ed2d7e89c463869 |
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sec-wf.cwl
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Path: tests/wf/sec-wf.cwl Branch/Commit ID: 2dce710246e091f0189fab41b589ee062ee94500 |
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Generate genome indices for STAR & bowtie
Creates indices for: * [STAR](https://github.com/alexdobin/STAR) v2.5.3a (03/17/2017) PMID: [23104886](https://www.ncbi.nlm.nih.gov/pubmed/23104886) * [bowtie](http://bowtie-bio.sourceforge.net/tutorial.shtml) v1.2.0 (12/30/2016) It performs the following steps: 1. `STAR --runMode genomeGenerate` to generate indices, based on [FASTA](http://zhanglab.ccmb.med.umich.edu/FASTA/) and [GTF](http://mblab.wustl.edu/GTF2.html) input files, returns results as an array of files 2. Outputs indices as [Direcotry](http://www.commonwl.org/v1.0/CommandLineTool.html#Directory) data type 3. Separates *chrNameLength.txt* file from Directory output 4. `bowtie-build` to generate indices requires genome [FASTA](http://zhanglab.ccmb.med.umich.edu/FASTA/) file as input, returns results as a group of main and secondary files |
Path: workflows/genome-indices.cwl Branch/Commit ID: 29bf638904709cfbf10908adcd51ba4886ace94a |
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advanced-header.cwl
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Path: metadata/advanced-header.cwl Branch/Commit ID: 44214a9d02e6d85b03eb708552ed812ae3d4a733 |
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scatter-wf2_v1_1.cwl
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Path: testdata/scatter-wf2_v1_1.cwl Branch/Commit ID: c1875d54dedc41b1d2fa08634dcf1caa8f1bc631 |
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Running cellranger count and lineage inference
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Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: a3e26136043c03192c38c335316d2d36e3e67478 |
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mut3.cwl
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Path: tests/wf/mut3.cwl Branch/Commit ID: fd6e054510e2bb65eed4069a3a88013d7ecbb99c |
