Explore Workflows
View already parsed workflows here or click here to add your own
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Cell Ranger Aggregate
Cell Ranger Aggregate ===================== |
![]() Path: workflows/cellranger-aggr.cwl Branch/Commit ID: 60854b5d299df91e135e05d02f4be61f6a310fbc |
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Subworkflow to allow calling different SV callers which require bam files as inputs
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![]() Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: 479c9b3e3fa32ec9c7cd4073cfbccc675fd254d9 |
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bwa_mem
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![]() Path: structuralvariants/cwl/subworkflows/bwa_mem.cwl Branch/Commit ID: 3f6a871f81f343cf81a345f73ff2eeac70804b8c |
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Cut-n-Run pipeline paired-end
Experimental pipeline for Cut-n-Run analysis. Uses mapping results from the following experiment types: - `chipseq-pe.cwl` - `trim-chipseq-pe.cwl` - `trim-atacseq-pe.cwl` Note, the upstream analyses should not have duplicates removed |
![]() Path: workflows/trim-chipseq-pe-cut-n-run.cwl Branch/Commit ID: c9e7f3de7f6ba38ee663bd3f9649e8d7dbac0c86 |
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wgs alignment and germline variant detection
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![]() Path: definitions/pipelines/germline_wgs.cwl Branch/Commit ID: 174f3b239018328cec1d821947438b457552724c |
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Motif Finding with HOMER with target and background regions from peaks
Motif Finding with HOMER with target and background regions from peaks --------------------------------------------------- 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-peak.cwl Branch/Commit ID: 4a5c59829ff8b9f3c843e66e3c675dcd9c689ed5 |
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strelkaSomaticVariantCaller_v0_1_1.cwl
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![]() Path: janis_pipelines/wgs_somatic/cwl/tools/strelkaSomaticVariantCaller_v0_1_1.cwl Branch/Commit ID: d3ae7483f860339a12c5f404de9db0f026571f77 |
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Non-Coding Bacterial Genes
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![]() Path: bacterial_noncoding/wf_bacterial_noncoding.cwl Branch/Commit ID: 4def84df33963fc9ac9d5c5f804b911d01a0d9ad |
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samtools_sort
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![]() Path: structuralvariants/cwl/subworkflows/samtools_sort.cwl Branch/Commit ID: de9cb009f8fe0c8d5a94db5c882cf21ddf372452 |
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animal-genome-assembly.cwl
Animal Genome Assembly pipeline by Kazuharu Arakawa (@gaou_ak) without assembly step by canu, CWLized by Tazro Ohta (@inutano) |
![]() Path: workflow/animal-genome-assembly/animal-genome-assembly.cwl Branch/Commit ID: 0cd20e1be620ae0817a1aa4286d73b78c89809f0 |