Explore Workflows
View already parsed workflows here or click here to add your own
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merge and annotate svs with population allele freq and vep
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: 0805e8e0d358136468e0a9f49e06005e41965adc |
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PGAP Pipeline
PGAP pipeline for external usage, powered via containers |
Path: wf_common.cwl Branch/Commit ID: 3e7a3c1cc1ed5164ae0a51a96f20d7c480d1d70b |
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Raw sequence data to BQSR
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Path: definitions/subworkflows/sequence_to_bqsr.cwl Branch/Commit ID: dc2c019c1aa24cc01b451a0f048cf94a35f163c4 |
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Bacterial Annotation, pass 2, blastp-based functional annotation (first pass)
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Path: bacterial_annot/wf_bacterial_annot_pass2.cwl Branch/Commit ID: 5c40c5a0464c84076e0e407a0e05522b43bdc0a6 |
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Run genomic CMsearch (Rfam rRNA)
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Path: bacterial_ncrna/wf_gcmsearch.cwl Branch/Commit ID: 7b21dc40840852f3942c31b9c472346ea3f9a3ca |
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SV filtering workflow
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Path: definitions/subworkflows/filter_sv_vcf.cwl Branch/Commit ID: 0805e8e0d358136468e0a9f49e06005e41965adc |
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spurious_annot pass2
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Path: spurious_annot/wf_spurious_annot_pass2.cwl Branch/Commit ID: 7b21dc40840852f3942c31b9c472346ea3f9a3ca |
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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: 0805e8e0d358136468e0a9f49e06005e41965adc |
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Exome QC workflow
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Path: definitions/subworkflows/qc_exome.cwl Branch/Commit ID: a670f323e77e02d9b77be9a13d73d5276dd3676c |
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chipseq-header.cwl
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Path: metadata/chipseq-header.cwl Branch/Commit ID: f343b7c2d377876476087491025bb6bf5152a004 |
