Explore Workflows
View already parsed workflows here or click here to add your own
| Graph | Name | Retrieved From | View |
|---|---|---|---|
|
|
env-wf1.cwl
|
Path: tests/env-wf1.cwl Branch/Commit ID: 707ebcd2173889604459c5f4ffb55173c508abb3 |
|
|
|
steplevel-resreq.cwl
|
Path: cwltool/schemas/v1.0/v1.0/steplevel-resreq.cwl Branch/Commit ID: 20d664eff23e59aa57908345bfdb1ceeab3438f2 |
|
|
|
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: 954bb2f213d97dfef1cddaf9e830169a92ad0c6b |
|
|
|
revsort-array.cwl
Reverse the lines in a document, then sort those lines. |
Path: input-data/revsort-array.cwl Branch/Commit ID: 4fd8e7dbcff5492cb32e4fb15263a51fa4490cf1 |
|
|
|
Varscan Workflow
|
Path: definitions/subworkflows/varscan_germline.cwl Branch/Commit ID: a670f323e77e02d9b77be9a13d73d5276dd3676c |
|
|
|
exome alignment with qc, no bqsr, no verify_bam_id
|
Path: definitions/pipelines/alignment_exome_nonhuman.cwl Branch/Commit ID: b465f0da2806ddb6df481409541d13288ccb40ec |
|
|
|
RNA-seq alelle specific pipeline for paired-end data
Allele specific RNA-Seq paired-end workflow |
Path: workflows/allele-rnaseq-pe.cwl Branch/Commit ID: c602e3cdd72ff904dd54d46ba2b5146eb1c57022 |
|
|
|
Single-Cell Preprocessing Pipeline
Devel version of Single-Cell Preprocessing Pipeline =================================================== |
Path: workflows/single-cell-preprocess.cwl Branch/Commit ID: cbefc215d8286447620664fb47076ba5d81aa47f |
|
|
|
allele-process-reference.cwl
|
Path: subworkflows/allele-process-reference.cwl Branch/Commit ID: e9a24699d8b5ffe64412b1ba0af8448c281b223a |
|
|
|
scatter-wf3_v1_2.cwl#main
|
Path: testdata/scatter-wf3_v1_2.cwl Branch/Commit ID: 77669d4dd1d1ebd2bdd9810f911608146d9b8e51 Packed ID: main |
