Explore Workflows
View already parsed workflows here or click here to add your own
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bams2cram.cwl
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Path: per-sample/Workflows/bams2cram.cwl Branch/Commit ID: 22a56d63bd3e05f484032b686d074cc15e3aeed0 |
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gp_makeblastdb
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Path: progs/gp_makeblastdb.cwl Branch/Commit ID: 4a44218a713aecc488359be275409414ae8c1434 |
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blastp_wnode_struct
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Path: task_types/tt_blastp_wnode_struct.cwl Branch/Commit ID: cc2f633532a6e0bc399b29180f25cc58ad5963d6 |
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PGAP Pipeline, simple user input, PGAPX-134
PGAP pipeline for external usage, powered via containers, simple user input: (FASTA + yaml only, no template) |
Path: pgap.cwl Branch/Commit ID: 1bf7dc7b03ea3c64e54375cc5c3767849a801000 |
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ChIP-seq peak caller workflow MACS2 based
This workflow execute peak caller and QC for ChIP-seq using MACS2 |
Path: workflows/ChIP-Seq/peak-calling-MACS2-PE-genome-size.cwl Branch/Commit ID: master |
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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: 3c7a6e39d956ca065751f23ee0316ac3f3306d9a |
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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: 3c7a6e39d956ca065751f23ee0316ac3f3306d9a |
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prepare_gencode_refs.cwl
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Path: workflow/prepare_gencode_refs.cwl Branch/Commit ID: master |
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wgs alignment and tumor-only variant detection
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Path: definitions/pipelines/wgs.cwl Branch/Commit ID: de81bd20ce8829ef64146115902a10e4fe7bad0b |
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811.cwl
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Path: tests/wf/811.cwl Branch/Commit ID: 4bb5329997cb84562a40733b5c2f55600b1a741a |
