Explore Workflows
View already parsed workflows here or click here to add your own
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genomics-workspace-transcript.cwl
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Path: flow_genomicsWorkspace/genomics-workspace-transcript.cwl Branch/Commit ID: 556884e8e205295e561b1d9140d836cdd6c1d8c9 |
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rnaseq-pe-dutp.cwl
Runs RNA-Seq BioWardrobe basic analysis with strand specific pair-end data file. |
Path: workflows/rnaseq-pe-dutp.cwl Branch/Commit ID: cf84038de256c7ca98657ad81734d1aca1dad8c1 |
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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: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
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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: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
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Raw sequence data to BQSR
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Path: definitions/subworkflows/sequence_to_bqsr.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
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WGS QC workflow
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Path: definitions/subworkflows/qc_wgs.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
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Merge, annotate, and generate a TSV for SVs
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Path: definitions/subworkflows/merge_svs.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
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Apply filters to VCF file
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Path: definitions/subworkflows/germline_filter_vcf.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
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rhapsody_pipeline_2.0.cwl#VDJ_Assemble_and_Annotate_Contigs_TCR.cwl
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Path: rhapsody_pipeline_2.0.cwl Branch/Commit ID: 50ed14112f9db254034dd5530cf1a768e04eb7ff Packed ID: VDJ_Assemble_and_Annotate_Contigs_TCR.cwl |
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WGS QC workflow nonhuman
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Path: definitions/subworkflows/qc_wgs_nonhuman.cwl Branch/Commit ID: 5fda2d9eb52a363bd51011b3851c2afb86318c0c |
