Explore Workflows
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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: 7518b100d8cbc80c8be32e9e939dfbb27d6b4361 |
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QuantSeq 3' FWD, FWD-UMI or REV for single-read mRNA-Seq data
### Devel version of QuantSeq 3' FWD, FWD-UMI or REV for single-read mRNA-Seq data |
Path: workflows/trim-quantseq-mrnaseq-se-strand-specific.cwl Branch/Commit ID: 7fb8a1ebf8145791440bc2fed9c5f2d78a19d04c |
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no-inputs-wf.cwl
Workflow without inputs. |
Path: tests/no-inputs-wf.cwl Branch/Commit ID: 5f27e234b4ca88ed1280dedf9e3391a01de12912 |
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mut3.cwl
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Path: tests/wf/mut3.cwl Branch/Commit ID: 4642316a30a95d4f3d135c18f98477886b160094 |
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allele-alignreads-se-pe.cwl
Workflow maps FASTQ files from `fastq_files` input into reference genome `reference_star_indices_folder` and insilico generated `insilico_star_indices_folder` genome (concatenated genome for both `strain1` and `strain2` strains). For both genomes STAR is run with `outFilterMultimapNmax` parameter set to 1 to discard all of the multimapped reads. For insilico genome SAM file is generated. Then it's splitted into two SAM files based on strain names and then sorted by coordinates into the BAM format. For reference genome output BAM file from STAR slignment is also coordinate sorted. |
Path: subworkflows/allele-alignreads-se-pe.cwl Branch/Commit ID: e238d1756f1db35571e84d72e1699e5d1540f10c |
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Generate ATDP heatmap using Homer
Generate ATDP heatmap centered on TSS from an array of input BAM files and genelist TSV file. Returns array of heatmap JSON files with the names that have the same basenames as input BAM files, but with .json extension |
Path: workflows/heatmap.cwl Branch/Commit ID: bfa3843bcf36125ff258d6314f64b41336f06e6b |
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QuantSeq 3' FWD, FWD-UMI or REV for single-read mRNA-Seq data
### Devel version of QuantSeq 3' FWD, FWD-UMI or REV for single-read mRNA-Seq data |
Path: workflows/trim-quantseq-mrnaseq-se-strand-specific.cwl Branch/Commit ID: e99e80a2c19682d59947bde04a892d7b6d90091c |
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mut2.cwl
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Path: tests/wf/mut2.cwl Branch/Commit ID: 520acbfb82455c4bdabd5f2ea24842804e1c9f58 |
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mpi_simple_wf.cwl
Simple 2 step workflow to check that workflow steps are independently picking up on the number of processes. First run the parallel get PIDs step (on the input num procs) then run (on a single proc) the line count. This should equal the input. |
Path: tests/wf/mpi_simple_wf.cwl Branch/Commit ID: eba80916b5cde8bdbd56c077c94240ddf796a27b |
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TAP
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Path: CWL/Workflows/tap.prok.workflow.cwl Branch/Commit ID: 107cdd243d21449459a2126ddc7a365da64a74c0 |
