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Showing results for "rnaseq" (Show all)

Graph	Name	Retrieved From	View
	rnaseq-pe-dutp.cwl RNA-Seq basic analysis workflow for strand specific paired-end experiment.	https://github.com/datirium/workflows.git Path: workflows/rnaseq-pe-dutp.cwl Branch/Commit ID: 4b8bb1a1ec39056253ca8eee976078e51f4a954e
	Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs	https://github.com/genome/analysis-workflows.git Path: definitions/pipelines/pvacseq.cwl Branch/Commit ID: ddb49a0951d9ad537269d7db3fe8f904495a8bf4
	trim-rnaseq-pe.cwl Runs RNA-Seq BioWardrobe basic analysis with pair-end data file.	https://github.com/Barski-lab/workflows.git Path: workflows/trim-rnaseq-pe.cwl Branch/Commit ID: c82a2e766abba032f0bbe2aa76e0176e69064569
	rnaseq-se-dutp.cwl RNA-Seq basic analysis workflow for strand specific single-read experiment.	https://github.com/datirium/workflows.git Path: workflows/rnaseq-se-dutp.cwl Branch/Commit ID: 4b8bb1a1ec39056253ca8eee976078e51f4a954e
	trim-rnaseq-pe-dutp.cwl Runs RNA-Seq BioWardrobe basic analysis with strand specific pair-end data file.	https://github.com/Barski-lab/workflows.git Path: workflows/trim-rnaseq-pe-dutp.cwl Branch/Commit ID: 812b0ff40dda18ab7a9a872ff13a577be8531ba6
	rnaseq-se.cwl Runs RNA-Seq BioWardrobe basic analysis with single-end data file.	https://github.com/Barski-lab/workflows.git Path: workflows/rnaseq-se.cwl Branch/Commit ID: 896422c9ff1995024cb77675edcd4d973ae11f7a
	trim-rnaseq-pe-dutp.cwl Runs RNA-Seq BioWardrobe basic analysis with strand specific pair-end data file.	https://github.com/Barski-lab/workflows.git Path: workflows/trim-rnaseq-pe-dutp.cwl Branch/Commit ID: 568da91bb1c6182ba4f146e2a729cac1c3d8783c
	trim-rnaseq-pe.cwl Runs RNA-Seq BioWardrobe basic analysis with pair-end data file.	https://github.com/Barski-lab/workflows.git Path: workflows/trim-rnaseq-pe.cwl Branch/Commit ID: 5a92b026bd62fe1597de940088e8adeef6939d5a
	rnaseq-se.cwl Runs RNA-Seq BioWardrobe basic analysis with single-end data file.	https://github.com/Barski-lab/workflows.git Path: workflows/rnaseq-se.cwl Branch/Commit ID: b4b7b2e7e508be5eac639f9e323d141daf714c0d
	Workflow to run pVACseq from detect_variants and rnaseq pipeline outputs	https://github.com/genome/analysis-workflows.git Path: definitions/subworkflows/pvacseq.cwl Branch/Commit ID: 6949082038c1ad36d6e9848b97a2537aef2d3805