Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and germline variant detection, with optitype for HLA typing
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![]() Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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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: a0b22644ca178b640fb74849d23b7c631022f0b5 |
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1st-workflow.cwl
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![]() Path: tests/wf/1st-workflow.cwl Branch/Commit ID: e6a1e1f3a3b3168028bd19aaf465826fa276a35b |
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Build Bismark indices
Copy fasta_file file to the folder and run run bismark_genome_preparation script to prepare indices for Bismark Methylation Analysis. Bowtie2 aligner is used by default. The name of the output indices folder is equal to the genome input. |
![]() Path: workflows/bismark-index.cwl Branch/Commit ID: a0b22644ca178b640fb74849d23b7c631022f0b5 |
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scatter-wf4.cwl#main
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![]() Path: v1.0/v1.0/scatter-wf4.cwl Branch/Commit ID: 4fe434e969c93c94b690ba72db295d9d52a6f576 Packed ID: main |
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directory.cwl
Inspect provided directory and return filenames. Generate a new directory and return it (including content). |
![]() Path: tests/wf/directory.cwl Branch/Commit ID: 7dec97bb8f0bc2d9e9eb710faf41f2e98cc7cdda |
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heatmap-prepare.cwl
Workflow runs homer-make-tag-directory.cwl tool using scatter for the following inputs - bam_file - fragment_size - total_reads `dotproduct` is used as a `scatterMethod`, so one element will be taken from each array to construct each job: 1) bam_file[0] fragment_size[0] total_reads[0] 2) bam_file[1] fragment_size[1] total_reads[1] ... N) bam_file[N] fragment_size[N] total_reads[N] `bam_file`, `fragment_size` and `total_reads` arrays should have the identical order. |
![]() Path: tools/heatmap-prepare.cwl Branch/Commit ID: 5e7385b8cfa4ddae822fff37b6bd22eb0370b389 |
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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: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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gather AML trio outputs
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![]() Path: definitions/pipelines/aml_trio_cle_gathered.cwl Branch/Commit ID: b8000c793d6e7ce4d690406c4f914c5c62acd51f |
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DiffBind - Differential Binding Analysis of ChIP-Seq Peak Data
Differential Binding Analysis of ChIP-Seq Peak Data --------------------------------------------------- DiffBind processes ChIP-Seq data enriched for genomic loci where specific protein/DNA binding occurs, including peak sets identified by ChIP-Seq peak callers and aligned sequence read datasets. It is designed to work with multiple peak sets simultaneously, representing different ChIP experiments (antibodies, transcription factor and/or histone marks, experimental conditions, replicates) as well as managing the results of multiple peak callers. For more information please refer to: ------------------------------------- Ross-Innes CS, Stark R, Teschendorff AE, Holmes KA, Ali HR, Dunning MJ, Brown GD, Gojis O, Ellis IO, Green AR, Ali S, Chin S, Palmieri C, Caldas C, Carroll JS (2012). “Differential oestrogen receptor binding is associated with clinical outcome in breast cancer.” Nature, 481, -4. |
![]() Path: workflows/diffbind.cwl Branch/Commit ID: a0b22644ca178b640fb74849d23b7c631022f0b5 |