Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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wf-alignment.cwl
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https://github.com/bcbio/test_bcbio_cwl.git
Path: somatic/somatic-workflow/wf-alignment.cwl Branch/Commit ID: 7ea627c4825d9840cd978a4d17aeb27edc04ae62 |
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mirna_profiling.cwl
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https://github.com/NCI-GDC/gdc-dnaseq-cwl.git
Path: workflows/mirnaseq/mirna_profiling.cwl Branch/Commit ID: 3cd06184444bb85e9773a3e7dc548c6dd3bdaccb |
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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) |
https://github.com/heliumdatacommons/TOPMed_RNAseq_CWL.git
Path: workflow/rnaseq_pipeline_fastq.cwl Branch/Commit ID: adc00cfb4abbeab5b975f28780dc50b7c1f555bd |
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wf-variantcall.cwl
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https://github.com/bcbio/test_bcbio_cwl.git
Path: somatic/somatic-workflow/wf-variantcall.cwl Branch/Commit ID: 7ea627c4825d9840cd978a4d17aeb27edc04ae62 |
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haplotypecaller.cwl
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https://github.com/uc-cdis/genomel_pipelines.git
Path: genomel/cwl/workflows/variant_calling/haplotypecaller.cwl Branch/Commit ID: 1595f2bc453663c9e71c1a2d60729f481921029e |
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download_prep.cwl
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https://github.com/uc-cdis/genomel_pipelines.git
Path: genomel/cwl/workflows/utils/download_prep.cwl Branch/Commit ID: 1595f2bc453663c9e71c1a2d60729f481921029e |
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gatk3_realignment.cwl
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https://github.com/uc-cdis/genomel_pipelines.git
Path: genomel/cwl/workflows/realignment/gatk3_realignment.cwl Branch/Commit ID: 1595f2bc453663c9e71c1a2d60729f481921029e |
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alignment_bwa_mem.cwl
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https://github.com/uc-cdis/genomel_pipelines.git
Path: genomel/cwl/workflows/harmonization/alignment_bwa_mem.cwl Branch/Commit ID: 1595f2bc453663c9e71c1a2d60729f481921029e |
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wf_makeblastdb.cwl
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https://github.com/ncbi/pipelines.git
Path: amr_finder/wf_makeblastdb.cwl Branch/Commit ID: 85bd1acfc587e6a3ebce7ccf1ce93bf8b48e881c |
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upload_results.cwl
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https://github.com/uc-cdis/genomel_pipelines.git
Path: genomel/cwl/workflows/utils/upload_results.cwl Branch/Commit ID: 1595f2bc453663c9e71c1a2d60729f481921029e |