Explore Workflows
View already parsed workflows here or click here to add your own
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chip_qc.cwl
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Path: CWL/workflow_modules/chip_qc.cwl Branch/Commit ID: 9ba07c9e24e49cd9cb21e6544d73b3f04316cf6f |
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exome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_exome.cwl Branch/Commit ID: 72c4c3115956340f35e72cda1fd46ec276f1ca03 |
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BLAST against rRNA db
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Path: bacterial_noncoding/wf_blastn.cwl Branch/Commit ID: 8a8fffb78b1e327ba0da51840ac8acc0c218d611 |
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gatk4_cohort_genotyping.cwl
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Path: genomel/cwl/workflows/variant_calling/gatk4_cohort_genotyping.cwl Branch/Commit ID: d777030ca3654fe78462ee69adcbd8221303b006 |
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freebayes.cwl
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Path: genomel/cwl/workflows/variant_calling/freebayes.cwl Branch/Commit ID: d777030ca3654fe78462ee69adcbd8221303b006 |
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mirna_profiling.cwl
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Path: workflows/mirnaseq/mirna_profiling.cwl Branch/Commit ID: a3eec6c1081d28efe00a0d269fb41303acc4ccdd |
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star_samtools_featurecounts_edger.cwl
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Path: workflows/star_samtools_featurecounts_edger.cwl Branch/Commit ID: 33a3cdba1184ad14e7a168eef3c505b9b4332f47 |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: f401b02285f30de1c12ac2859134099fe04be33f |
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merge and annotate svs with population allele freq
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: f401b02285f30de1c12ac2859134099fe04be33f |
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basename-fields-test.cwl
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Path: v1.0/v1.0/basename-fields-test.cwl Branch/Commit ID: 8c35118bbcd2b125635dcdfb16a09e09bbfd4015 |
