Explore Workflows
View already parsed workflows here or click here to add your own
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animal-genome-assembly.packed.cwl#main
Animal Genome Assembly pipeline by Kazuharu Arakawa (@gaou_ak) without assembly step by canu, CWLized by Tazro Ohta (@inutano) |
Path: workflow/animal-genome-assembly/animal-genome-assembly.packed.cwl Branch/Commit ID: main Packed ID: main |
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count-lines11-wf-noET.cwl
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Path: tests/count-lines11-wf-noET.cwl Branch/Commit ID: master |
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topmed-alignment.cwl
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Path: aligner/sbg-alignment-cwl/topmed-alignment.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: fa86fce |
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wf-alignment.cwl
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Path: somatic-giab-mix/somatic-giab-mix-workflow/wf-alignment.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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umi molecular alignment workflow
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Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: downsample_and_recall |
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wrf_workflow.cwl
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Path: workflows/wrf_workflow.cwl Branch/Commit ID: develop |
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Detect whitelisted variants
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Path: subworkflows/whitelist.cwl Branch/Commit ID: master |
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strelkaSomaticVariantCaller_v0_1_1.cwl
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Path: janis_pipelines/wgs_somatic/cwl/tools/strelkaSomaticVariantCaller_v0_1_1.cwl Branch/Commit ID: master |
