Explore Workflows
View already parsed workflows here or click here to add your own
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workflow.cwl
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![]() Path: bioinformatics/tools/workflow.cwl Branch/Commit ID: master |
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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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STAR-Alignment-PE
This workflow aligns the fastq files using STAR for no spliced genomes |
![]() Path: workflows/Alignments/star-alignment-nosplice.cwl Branch/Commit ID: b5a440939ac6022ee81aeeb0dd7daf3983228a61 |
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conflict.cwl#main
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![]() Path: tests/wf/conflict.cwl Branch/Commit ID: main Packed ID: main |
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ValidateTriggerPerformance
Compare trigger performance between simulations and data. |
![]() Path: workflows/ValidateTriggerPerformance.cwl Branch/Commit ID: main |
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wf_demultiplex_se.cwl
This workflow takes in single-end reads, and performs the following steps in order: demux_se.cwl (does not actually demux for single end, but mirrors the paired-end processing protocol) |
![]() Path: cwl/wf_demultiplex_se.cwl Branch/Commit ID: master |
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batch-preprocess-ont.cwl
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![]() Path: PreProcessing/batch-preprocess-ont.cwl Branch/Commit ID: master |
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rna-seq-pipeline.cwl
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![]() Path: gtex-rnaseq-pipeline/rna-seq-pipeline.cwl Branch/Commit ID: master |
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02-trim-se.cwl
RNA-seq 02 trimming - reads: SE |
![]() Path: v1.0/RNA-seq_pipeline/02-trim-se.cwl Branch/Commit ID: master |
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revsort.cwl
Reverse the lines in a document, then sort those lines. |
![]() Path: tests/wf/revsort.cwl Branch/Commit ID: main |