Explore Workflows
View already parsed workflows here or click here to add your own
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Exome QC workflow
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Path: definitions/subworkflows/qc_exome_no_verify_bam.cwl Branch/Commit ID: 6949082038c1ad36d6e9848b97a2537aef2d3805 |
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Filter differentially expressed genes from DESeq for Tag Density Profile Analyses
Filters differentially expressed genes from DESeq for Tag Density Profile Analyses ================================================================================== Tool filters output from DESeq pipeline run for genes to create a file with regions of interest for Tag Density Profile Analyses. |
Path: workflows/filter-deseq-for-heatmap.cwl Branch/Commit ID: 480e99a4bb3046e0565113d9dca294e0895d3b0c |
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Genomic regions intersection and visualization
Genomic regions intersection and visualization ============================================== 1. Merges intervals within each of the filtered peaks files from ChIP/ATAC experiments 2. Overlaps merged intervals and assigns the nearest genes to them |
Path: workflows/intervene.cwl Branch/Commit ID: 480e99a4bb3046e0565113d9dca294e0895d3b0c |
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Add snv and indel bam-readcount files to a vcf
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Path: definitions/subworkflows/vcf_readcount_annotator.cwl Branch/Commit ID: 788bdc99c1d5b6ee7c431c3c011eb30d385c1370 |
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workflow.cwl
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Path: flow_dispatch/2working_files/workflow.cwl Branch/Commit ID: 78d6c8be6c033774839fd68a0b5e643d4592489c |
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checker_workflow.cwl
Description of checker workflow here |
Path: checker_workflow.cwl Branch/Commit ID: fb42c673c20df2f91cb7cfebe52254efcda5657f |
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umi per-lane alignment subworkflow
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Path: definitions/subworkflows/umi_alignment.cwl Branch/Commit ID: 6949082038c1ad36d6e9848b97a2537aef2d3805 |
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foreign_screening.cwl
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Path: vecscreen/foreign_screening.cwl Branch/Commit ID: 5e92165ac2c11608ab2db42fe2d66eabe72dbb40 |
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exome alignment and somatic variant detection for cle purpose
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Path: definitions/pipelines/somatic_exome_cle.cwl Branch/Commit ID: 788bdc99c1d5b6ee7c431c3c011eb30d385c1370 |
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THOR - differential peak calling of ChIP-seq signals with replicates
What is THOR? -------------- THOR is an HMM-based approach to detect and analyze differential peaks in two sets of ChIP-seq data from distinct biological conditions with replicates. THOR performs genomic signal processing, peak calling and p-value calculation in an integrated framework. For more information please refer to: ------------------------------------- Allhoff, M., Sere K., Freitas, J., Zenke, M., Costa, I.G. (2016), Differential Peak Calling of ChIP-seq Signals with Replicates with THOR, Nucleic Acids Research, epub gkw680. |
Path: workflows/rgt-thor.cwl Branch/Commit ID: 9e3c3e65c19873cd1ed3cf7cc3b94ebc75ae0cc5 |
