Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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phase VCF
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![]() Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: 54846feabbf008c1946db2a86d87252e0edd95b0 |
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RNA-Seq alignment and transcript/gene abundance workflow
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![]() Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 54846feabbf008c1946db2a86d87252e0edd95b0 |
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: 742dbafb5fb103d8578f48a0576c14dd8dae3b2a |
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bam to trimmed fastqs
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![]() Path: definitions/subworkflows/bam_to_trimmed_fastq.cwl Branch/Commit ID: 742dbafb5fb103d8578f48a0576c14dd8dae3b2a |
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Coverage_generator.cwl
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![]() Path: workflows/Coverage_generator.cwl Branch/Commit ID: 61fc6a32a38aabc111a5841ec7792abe9a53a25f |
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Filter single sample sv vcf from paired read callers(Manta/Smoove)
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![]() Path: definitions/subworkflows/sv_paired_read_caller_filter.cwl Branch/Commit ID: 74647cc0f1abac4ee22950cfa89c44cf2ca3cffd |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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![]() Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: 74647cc0f1abac4ee22950cfa89c44cf2ca3cffd |
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exome alignment with qc
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![]() Path: definitions/pipelines/alignment_exome.cwl Branch/Commit ID: 233f026ffce240071edda526391be0c03186fce8 |
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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: 74647cc0f1abac4ee22950cfa89c44cf2ca3cffd |
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Detect Variants workflow
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![]() Path: definitions/pipelines/detect_variants.cwl Branch/Commit ID: 233f026ffce240071edda526391be0c03186fce8 |