Explore Workflows
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Showing results for "rnaseq" (Show all)
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: f615832615c3b41728df8e47b72ef11e37e6a9e5 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 97572e3a088d79f6a4166385f79e79ea77b11470 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: ecac0fda44df3a8f25ddfbb3e7a023fcbe4cbd0f |
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rnaseq-se.cwl
RNA-Seq basic analysis workflow for single-read experiment. |
https://github.com/datirium/workflows.git
Path: workflows/rnaseq-se.cwl Branch/Commit ID: 62323c137c0ce9b3f843df0dfbda28dafa7c90cf |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: cc3e7f1ccfdc7101c22bf88792608504eea7d53a |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 77ec4f26eb14ed82481828bd9f6ef659cfd8b40f |
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xenbase-rnaseq-pe.cwl
XenBase workflow for analysing RNA-Seq paired-end data |
https://github.com/datirium/workflows.git
Path: workflows/xenbase-rnaseq-pe.cwl Branch/Commit ID: a9551ece898f619167db58e4b74a6cae2d7f7d13 |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: d3e4bf55753cd92f97537c7d701187ea92d1e5f0 |
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allele-vcf-rnaseq-se.cwl
Allele specific RNA-Seq (using vcf) single-read workflow |
https://github.com/datirium/workflows.git
Path: workflows/allele-vcf-rnaseq-se.cwl Branch/Commit ID: 62323c137c0ce9b3f843df0dfbda28dafa7c90cf |
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Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs
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https://github.com/genome/analysis-workflows.git
Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 4aba7c6591c2f1ebd827a36d325a58738c429bea |
