Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and germline variant detection, with optitype for HLA typing
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Path: definitions/pipelines/germline_exome_hla_typing.cwl Branch/Commit ID: 8438316338e66823e1c9aca9f675b2bf33f2aa59 |
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umi molecular alignment workflow
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Path: definitions/subworkflows/molecular_qc.cwl Branch/Commit ID: 788bdc99c1d5b6ee7c431c3c011eb30d385c1370 |
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count-lines6-wf.cwl
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Path: cwltool/schemas/v1.0/v1.0/count-lines6-wf.cwl Branch/Commit ID: bfe56f3138e9e6fc0b9b8c06447553d4cea03d59 |
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Detect DoCM variants
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Path: definitions/subworkflows/docm_germline.cwl Branch/Commit ID: 4a04ad33e311c5e647cef848b74034477cb3c47e |
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Detect Variants workflow for nonhuman WGS pipeline
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Path: definitions/pipelines/detect_variants_wgs_nonhuman.cwl Branch/Commit ID: d57c2af01a3cb6016e5a264f60641eafd2e5aa05 |
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any-type-compat.cwl
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Path: cwltool/schemas/v1.0/v1.0/any-type-compat.cwl Branch/Commit ID: 10492acee927c177933160f6ad67085f9112b0d1 |
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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: bc75349ad3a7bdce82b4cd8584501f4d0280bb8d |
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Unaligned BAM to BQSR
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Path: definitions/subworkflows/bam_to_bqsr.cwl Branch/Commit ID: 0db1a5f1ceedd4416ac550787c27b99c87dbe985 |
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gather AML trio outputs
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Path: definitions/pipelines/aml_trio_cle_gathered.cwl Branch/Commit ID: 8438316338e66823e1c9aca9f675b2bf33f2aa59 |
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xenbase-sra-to-fastq-se.cwl
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Path: subworkflows/xenbase-sra-to-fastq-se.cwl Branch/Commit ID: b25b17651171f32005e9d879a9a049382f044baf |
