Explore Workflows
View already parsed workflows here or click here to add your own
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align_sort_sa
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Path: task_types/tt_align_sort_sa.cwl Branch/Commit ID: a402541b8530f30eab726c160da90a23036847a1 |
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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: 46a077b51619c6a14f85e0aa5260ae8a04426fab |
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Cellranger Reanalyze
Cellranger Reanalyze ==================== |
Path: workflows/cellranger-reanalyze.cwl Branch/Commit ID: f3e44d3b0f198cf5245c49011124dc3b6c2b06fd |
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tt_blastn_wnode
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Path: task_types/tt_blastn_wnode.cwl Branch/Commit ID: d218e081d8f6a4fdab56a38ce0fc2fae6216cecc |
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mut.cwl
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Path: tests/wf/mut.cwl Branch/Commit ID: ec2cf2da6c31ffedf827a0fb213b5204e172f510 |
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Filter differentially expressed genes from DESeq for Tag Density Profile Analyses
Filters differentially expressed genes from DESeq for Tag Density Profile Analyses ================================================================================== Tool filters output from DESeq pipeline run for genes to create a file with regions of interest for Tag Density Profile Analyses. |
Path: workflows/filter-deseq-for-heatmap.cwl Branch/Commit ID: 36fd18f11e939d3908b1eca8d2939402f7a99b0f |
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ani_top_n
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Path: task_types/tt_ani_top_n.cwl Branch/Commit ID: 68058b108cb5b0b72ebe244c42eefa2747e1d64a |
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THOR - differential peak calling of ChIP-seq signals with replicates
What is THOR? -------------- THOR is an HMM-based approach to detect and analyze differential peaks in two sets of ChIP-seq data from distinct biological conditions with replicates. THOR performs genomic signal processing, peak calling and p-value calculation in an integrated framework. For more information please refer to: ------------------------------------- Allhoff, M., Sere K., Freitas, J., Zenke, M., Costa, I.G. (2016), Differential Peak Calling of ChIP-seq Signals with Replicates with THOR, Nucleic Acids Research, epub gkw680. |
Path: workflows/rgt-thor.cwl Branch/Commit ID: 93b844a80f4008cc973ea9b5efedaff32a343895 |
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DiffBind - Differential Binding Analysis of ChIP-Seq or CUTß&RUN/Tag Peak Data
Differential Binding Analysis of ChIP-Seq or CUT&RUN/Tag Peak Data --------------------------------------------------- DiffBind processes ChIP-Seq or CUT&RUN/Tag data enriched for genomic loci where specific protein/DNA binding occurs, including peak sets identified by peak caller tools and aligned sequence read datasets. It is designed to work with multiple peak sets simultaneously, representing different ChIP or CUT&RUN/Tag 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.cwl Branch/Commit ID: 93b844a80f4008cc973ea9b5efedaff32a343895 |
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HS Metrics workflow
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Path: definitions/subworkflows/hs_metrics.cwl Branch/Commit ID: 31602b94b34ff55876147c7299e1bec47e8d1a31 |
