Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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cram_to_bam workflow
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https://github.com/markrobbo/workflows.git
Path: workflows/hello/exome_alignment_packed.cwl Branch/Commit ID: master Packed ID: workflow.cwl |
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Find reads with predicted coding sequences above 60 AA in length
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https://github.com/proteinswebteam/ebi-metagenomics-cwl.git
Path: workflows/orf_prediction.cwl Branch/Commit ID: master |
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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/) |
https://github.com/datirium/workflows.git
Path: workflows/homer-motif-analysis-peak.cwl Branch/Commit ID: bf80c9339d81a78aefb8de661bff998ed86e836e |
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cnv_gridss
CNV GRIDSS calling |
https://gitlab.bsc.es/lrodrig1/structuralvariants_poc.git
Path: structuralvariants/subworkflows/cnv_gridss.cwl Branch/Commit ID: 3bb03c9b |
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conpair-master
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https://github.com/mskcc/roslin-variant.git
Path: setup/cwl/conpair/0.2/conpair-master.cwl Branch/Commit ID: 2.4.x |
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wf_clipseqcore_nostats_se_1barcode.cwl
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https://github.com/YeoLab/eclip.git
Path: cwl/wf_clipseqcore_nostats_se_1barcode.cwl Branch/Commit ID: master |
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workflow.cwl
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https://gitlab.ebrains.eu/sofiakar/yre-standardised-workflows.git
Path: Workflows/PSD_workflow_smr_1/workflow.cwl Branch/Commit ID: main |
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wf_trim_partial_and_map_se_scatter.cwl
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https://github.com/yeolab/eclip.git
Path: cwl/wf_trim_partial_and_map_se_scatter.cwl Branch/Commit ID: master |
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Per-chromosome pindel
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https://github.com/hamid58b/cancer-genomics-workflow.git
Path: pindel/pindel_cat.cwl Branch/Commit ID: master |
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cnv_manta
CNV Manta calling |
https://gitlab.bsc.es/lrodrig1/structuralvariants_poc.git
Path: structuralvariants/subworkflows/cnv_manta.cwl Branch/Commit ID: 3bb03c9b |