Explore Workflows
View already parsed workflows here or click here to add your own
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TOPMed_RNA-seq
TOPMed RNA-seq CWL workflow. Documentation on the workflow can be found [here](https://github.com/heliumdatacommons/TOPMed_RNAseq_CWL/blob/master/README.md). Example input files: [Dockstore.json](https://github.com/heliumdatacommons/TOPMed_RNAseq_CWL/blob/master/workflow/input-examples/Dockstore.json) and [rnaseq_pipeline_fastq-example.yml](https://github.com/heliumdatacommons/TOPMed_RNAseq_CWL/blob/master/workflow/input-examples/rnaseq_pipeline_fastq-example.yml). Quickstart instructions are [here](https://github.com/heliumdatacommons/TOPMed_RNAseq_CWL/README.md#Quick Start). [GitHub Repo](https://github.com/heliumdatacommons/TOPMed_RNAseq_CWL) Pipeline steps: 1. Align RNA-seq reads with [STAR v2.5.3a](https://github.com/alexdobin/STAR). 2. Run [Picard](https://github.com/broadinstitute/picard) [MarkDuplicates](https://broadinstitute.github.io/picard/command-line-overview.html#MarkDuplicates). 2a. Create BAM index for MarkDuplicates BAM with [Samtools 1.6](https://github.com/samtools/samtools/releases) index. 3. Transcript quantification with [RSEM 1.3.0](https://deweylab.github.io/RSEM/) 4. Gene quantification and quality control with [RNA-SeQC 1.1.9](https://github.com/francois-a/rnaseqc) |
Path: workflow/rnaseq_pipeline_fastq.cwl Branch/Commit ID: master |
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snapanalysis_setup_and_analyze.cwl
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Path: steps/snapanalysis_setup_and_analyze.cwl Branch/Commit ID: 44dbe38 |
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preprocessor_for_oxog.cwl
This workflow will perform preprocessing steps on VCFs for the OxoG/Variantbam/Annotation workflow. |
Path: preprocessor_for_oxog.cwl Branch/Commit ID: master |
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test-data.cwl
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Path: test-data.cwl Branch/Commit ID: master |
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collate_unique_SSU_headers.cwl
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Path: tools/collate_unique_SSU_headers.cwl Branch/Commit ID: 43d2fb8 |
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CODEX analysis pipeline using Cytokit
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Path: pipeline.cwl Branch/Commit ID: 2d9ddc6 |
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main-pisces-titr.cwl
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Path: somatic-lowfreq/pisces-titr-workflow/main-pisces-titr.cwl Branch/Commit ID: master |
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ChIP-seq peak caller workflow MACS2 based
This workflow execute peak caller and QC for ChIP-seq using MACS2 |
Path: workflows/ChIP-Seq/peak-calling-MACS2.cwl Branch/Commit ID: master |
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rnaseq-star-rsem-pe.cwl
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Path: workflow/rna-seq/rnaseq-star-rsem-pe/rnaseq-star-rsem-pe.cwl Branch/Commit ID: main |
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SetReadoutPulseShape
Set FADC pulse for high and low-gain channel. Apply transformations required by the simulation model (e.g., normalization, time shift) |
Path: workflows/SetReadoutPulseShape.cwl Branch/Commit ID: main |
