Explore Workflows
View already parsed workflows here or click here to add your own
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echo-wf-default.cwl
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![]() Path: v1.0/v1.0/echo-wf-default.cwl Branch/Commit ID: 17695244222b0301b37cb749fe4a8d89622cd1ad |
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any-type-compat.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/any-type-compat.cwl Branch/Commit ID: 203797516329f7fb8aa5e763e6f9b331c63c3060 |
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SoupX (workflow) - an R package for the estimation and removal of cell free mRNA contamination
Wrapped in a workflow SoupX tool for easy access to Cell Ranger pipeline compressed outputs. |
![]() Path: tools/soupx-subworkflow.cwl Branch/Commit ID: 30031ca5e69cec603c4733681de54dc7bffa20a3 |
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revsort_step_bad_schema.cwl
Reverse the lines in a document, then sort those lines. |
![]() Path: tests/wf/revsort_step_bad_schema.cwl Branch/Commit ID: f94719e862f86cc88600caf3628faba6c0d05042 |
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Cellranger Reanalyze
Cellranger Reanalyze ==================== |
![]() Path: workflows/cellranger-reanalyze.cwl Branch/Commit ID: 30031ca5e69cec603c4733681de54dc7bffa20a3 |
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List ZIP content for zenodo community
For a given Zenodo community, list file content of its downloadable *.zip files |
![]() Path: code/data-gathering/workflows/zenodo-zip-content.cwl Branch/Commit ID: c0afa9b82e29ee0dfa83e903784ee54479567920 |
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01-qc-pe.cwl
ATAC-seq 01 QC - reads: PE |
![]() Path: v1.0/ATAC-seq_pipeline/01-qc-pe.cwl Branch/Commit ID: 6e68bda2cb45e8dc8e4d067c4220d65acfa53065 |
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Motif Finding with HOMER with custom background regions
Motif Finding with HOMER with custom background regions --------------------------------------------------- HOMER contains a novel motif discovery algorithm that was designed for regulatory element analysis in genomics applications (DNA only, no protein). It is a differential motif discovery algorithm, which means that it takes two sets of sequences and tries to identify the regulatory elements that are specifically enriched in on set relative to the other. It uses ZOOPS scoring (zero or one occurrence per sequence) coupled with the hypergeometric enrichment calculations (or binomial) to determine motif enrichment. HOMER also tries its best to account for sequenced bias in the dataset. It was designed with ChIP-Seq and promoter analysis in mind, but can be applied to pretty much any nucleic acids motif finding problem. For more information please refer to: ------------------------------------- [Official documentation](http://homer.ucsd.edu/homer/motif/) |
![]() Path: workflows/homer-motif-analysis-bg.cwl Branch/Commit ID: 30031ca5e69cec603c4733681de54dc7bffa20a3 |
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conflict-wf.cwl#collision
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![]() Path: cwltool/schemas/v1.0/v1.0/conflict-wf.cwl Branch/Commit ID: 49cd284a8fc7884de763573075d3e1d6a4c1ffdd Packed ID: collision |
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DESeq - differential gene expression analysis
Differential gene expression analysis ===================================== Differential gene expression analysis based on the negative binomial distribution Estimate variance-mean dependence in count data from high-throughput sequencing assays and test for differential expression based on a model using the negative binomial distribution. DESeq1 ------ High-throughput sequencing assays such as RNA-Seq, ChIP-Seq or barcode counting provide quantitative readouts in the form of count data. To infer differential signal in such data correctly and with good statistical power, estimation of data variability throughout the dynamic range and a suitable error model are required. Simon Anders and Wolfgang Huber propose a method based on the negative binomial distribution, with variance and mean linked by local regression and present an implementation, [DESeq](http://bioconductor.org/packages/release/bioc/html/DESeq.html), as an R/Bioconductor package DESeq2 ------ In comparative high-throughput sequencing assays, a fundamental task is the analysis of count data, such as read counts per gene in RNA-seq, for evidence of systematic changes across experimental conditions. Small replicate numbers, discreteness, large dynamic range and the presence of outliers require a suitable statistical approach. [DESeq2](http://www.bioconductor.org/packages/release/bioc/html/DESeq2.html), a method for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates. This enables a more quantitative analysis focused on the strength rather than the mere presence of differential expression. |
![]() Path: workflows/deseq.cwl Branch/Commit ID: 30031ca5e69cec603c4733681de54dc7bffa20a3 |