Explore Workflows
View already parsed workflows here or click here to add your own
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kmer_top_n_extract
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Path: task_types/tt_kmer_top_n_extract.cwl Branch/Commit ID: dev |
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Bisulfite QC tools
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Path: definitions/subworkflows/bisulfite_qc.cwl Branch/Commit ID: low-vaf |
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word-mapping-dir.cwl#word-mapping-wf.cwl
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Path: ochre/cwl/word-mapping-dir.cwl Branch/Commit ID: master Packed ID: word-mapping-wf.cwl |
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scatter-two-steps.cwl
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Path: _includes/cwl/scatter-two-steps.cwl Branch/Commit ID: gh-pages |
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tt_kmer_top_n.cwl
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Path: task_types/tt_kmer_top_n.cwl Branch/Commit ID: dev |
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Whole Genome Sequence processing workflow scattered over samples
<p>This is a “real-world” workflow example for processing Next Generation Sequencing (NGS) Whole Genome Sequence (WGS) data.</p> <p>You can learn more and run this workflow yourself by going through the <a href=\"https://doc.arvados.org/main/user/tutorials/wgs-tutorial.html\">Processing Whole Genome Sequences</a> walkthrough in the Arvados user guide.</p> <p>The steps of this workflow include:</p> <ol> <li>Check of fastq quality using FastQC</li> <li>Local alignment using BWA-MEM</li> <li>Variant calling in parallel using GATK Haplotype Caller</li> <li>Generation of an HTML report comparing variants against ClinVar archive</li> </ol> <p>The primary input parameter is the <b>Directory of paired FASTQ files</b>, which should contain paired FASTQ files (suffixed with _1 and _2) to be processed. The workflow scatters over the samples to process them in parallel.</p> <p>The remaining parameters are reference data used by various tools in the pipeline.</p> |
Path: WGS-processing/cwl/wgs-processing-wf.cwl Branch/Commit ID: main |
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timelimit-wf.cwl
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Path: tests/timelimit-wf.cwl Branch/Commit ID: main |
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geogrid_workflow.cwl
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Path: workflows/geogrid_workflow.cwl Branch/Commit ID: develop |
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msa.cwl
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Path: msa.cwl Branch/Commit ID: master |
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count-lines11-null-step-wf.cwl
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Path: tests/count-lines11-null-step-wf.cwl Branch/Commit ID: main |
