Explore Workflows
View already parsed workflows here or click here to add your own
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scatter-wf4.cwl#main
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Path: tests/wf/scatter-wf4.cwl Branch/Commit ID: 6003cbb94f16103241b562f2133e7c4acac6c621 Packed ID: main |
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Varscan Workflow
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Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: 72e0bdc1ec449d86df4534132e9a30ad7e9b8afd |
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heatmap.cwl
Generates 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: 94471ee6c01b7bc17102e45e56e7366c2a52acdf |
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rnaseq-se-dutp.cwl
RNA-Seq basic analysis workflow for strand specific single-read experiment. |
Path: workflows/rnaseq-se-dutp.cwl Branch/Commit ID: 62323c137c0ce9b3f843df0dfbda28dafa7c90cf |
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allele-process-reference.cwl
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Path: subworkflows/allele-process-reference.cwl Branch/Commit ID: e238d1756f1db35571e84d72e1699e5d1540f10c |
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exomeseq-00-prepare-reference-data.cwl
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Path: subworkflows/exomeseq-00-prepare-reference-data.cwl Branch/Commit ID: 92b8d41bab2661919aa11aa84e1923748f8503c4 |
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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: 7518b100d8cbc80c8be32e9e939dfbb27d6b4361 |
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Generate genome index STAR RNA
Workflow makes indices for [STAR](https://github.com/alexdobin/STAR) v2.5.3a (03/17/2017) PMID: [23104886](https://www.ncbi.nlm.nih.gov/pubmed/23104886). It performs the following steps: 1. Runs `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. Transforms array of files into [Direcotry](http://www.commonwl.org/v1.0/CommandLineTool.html#Directory) data type 3. Separates *chrNameLength.txt* file as an output |
Path: workflows/star-index.cwl Branch/Commit ID: bfa3843bcf36125ff258d6314f64b41336f06e6b |
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QuantSeq 3' FWD, FWD-UMI or REV for single-read mRNA-Seq data
### Devel version of QuantSeq 3' FWD, FWD-UMI or REV for single-read mRNA-Seq data |
Path: workflows/trim-quantseq-mrnaseq-se-strand-specific.cwl Branch/Commit ID: a409db2289b86779897ff19003bd351701a81c50 |
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rnaseq-alignment-quantification
This workflow retrieve SRA fastqc data and execute QC, alignment and quantification from TPMCalculator |
Path: workflows/RNA-Seq/rnaseq-quantification-qc.cwl Branch/Commit ID: e541470bc9d0b064bc4ed7dd2b45d8ec67760613 |
