Explore Workflows
View already parsed workflows here or click here to add your own
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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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group-isoforms-batch.cwl
Workflow runs group-isoforms.cwl tool using scatter for isoforms_file input. genes_filename and common_tss_filename inputs are ignored. |
Path: tools/group-isoforms-batch.cwl Branch/Commit ID: license_test |
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count-lines1-wf.cwl
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Path: tests/count-lines1-wf.cwl Branch/Commit ID: main |
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TOPMed_RNA-seq
TOPMed RNA-seq CWL workflow. Documentation on the workflow can be found [here](https://github.com/heliumdatacommons/cwl_workflows/blob/master/topmed-workflows/TOPMed_RNAseq_pipeline/README.md). Example input files: [Dockstore.json](https://github.com/heliumdatacommons/cwl_workflows/blob/master/topmed-workflows/TOPMed_RNAseq_pipeline/input-examples/Dockstore.json) and [rnaseq_pipeline_fastq-example.yml](https://github.com/heliumdatacommons/cwl_workflows/blob/master/topmed-workflows/TOPMed_RNAseq_pipeline/input-examples/rnaseq_pipeline_fastq-example.yml). Quickstart instructions are [here](https://github.com/heliumdatacommons/cwl_workflows/blob/master/topmed-workflows/TOPMed_RNAseq_pipeline/README.md#Quick Start). [GitHub Repo](https://github.com/heliumdatacommons/cwl_workflows) 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: topmed-workflows/TOPMed_RNAseq_pipeline/rnaseq_pipeline_fastq.cwl Branch/Commit ID: CWLProvTesting |
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env-wf3.cwl
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Path: tests/env-wf3.cwl Branch/Commit ID: master |
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rRNA_selection.cwl
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Path: tools/rRNA_selection.cwl Branch/Commit ID: 9c57dba |
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scRNA-seq pipeline using Salmon and Alevin
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Path: pipeline.cwl Branch/Commit ID: release |
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Unaligned to aligned BAM
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Path: unaligned_bam_to_bqsr/align.cwl Branch/Commit ID: toil_compatibility |
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Production Configuration
This workflow prepares the configuration of the subsequent production steps. |
Path: workflows/wms/uc-wms-XXX.cwl Branch/Commit ID: main |
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Running cellranger count and lineage inference
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Path: definitions/subworkflows/single_cell_rnaseq.cwl Branch/Commit ID: master |
