Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
---|---|---|---|
|
scRNA-seq pipeline using Salmon and Alevin
|
![]() Path: pipeline.cwl Branch/Commit ID: c502823c0b078737ef4533b1509e25d58cb3a78a |
|
|
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: 9850a859de1f42d3d252c50e15701928856fe774 |
|
|
metrics-flow.cwl
Run metrics workflow |
![]() Path: stage/metrics-flow.cwl Branch/Commit ID: 845f4699c5fce96a4c708a553b3701c9cf296653 |
|
|
js-expr-req-wf.cwl#wf
|
![]() Path: v1.0/v1.0/js-expr-req-wf.cwl Branch/Commit ID: e67f19d8a713759d761ecad050966d1eb043b85c Packed ID: wf |
|
|
Single-Cell Preprocessing Cell Ranger Pipeline
Devel version of Single-Cell Preprocessing Cell Ranger Pipeline =============================================================== |
![]() Path: workflows/single-cell-preprocess-cellranger.cwl Branch/Commit ID: 104059e07a2964673e21d371763e33c0afeb2d03 |
|
|
scatter-wf4.cwl#main
|
![]() Path: v1.0/v1.0/scatter-wf4.cwl Branch/Commit ID: f02557902989c749c9c2187c7045e340e2d76bfc Packed ID: main |
|
|
Build Bowtie indices
Workflow runs [Bowtie](http://bowtie-bio.sourceforge.net/tutorial.shtml) v1.2.0 (12/30/2016) to build indices for reference genome provided in a single FASTA file as fasta_file input. Generated indices are saved in a folder with the name that corresponds to the input genome |
![]() Path: workflows/bowtie-index.cwl Branch/Commit ID: 799575ce58746813f066a665adeacdda252d8cab |
|
|
spurious_annot
|
![]() Path: spurious_annot/wf_spurious_annot_pass1.cwl Branch/Commit ID: 5463361069e263ad6455858e054c1337b1d9e752 |
|
|
tnhc-distr.cwl
|
![]() Path: stage/tnhc-distr.cwl Branch/Commit ID: 845f4699c5fce96a4c708a553b3701c9cf296653 |
|
|
bam to trimmed fastqs and HISAT alignments
|
![]() Path: definitions/subworkflows/bam_to_trimmed_fastq_and_hisat_alignments.cwl Branch/Commit ID: 3042812447d9e8889c6118986490e9c9b9b13223 |