runArriba: Run Arriba on RNA-Seq samples using structural-variants...

Description Usage Arguments Value Author(s) See Also Examples

View source: R/analysisRNA_runArriba.R

Description

Run Arriba on RNA-Seq samples using structural-variants information derived from WGS.

Usage

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runArriba(data.SV, minTAF = 0.05, bamFolder, outputFolder)

Arguments

data.SV

(GRanges): GRanges of SV derived from WGS.

minTAF

(integer): Min. TAF of SV to take into the analysis, set to zero (0) for no filtering.

bamFolder

(character): Path to folder containing the RNA-Seq BAM files (STAR).

outputFolder

(character): Path to folder to write Arriba output.

Value

(chr) Command to run Arriba.

Author(s)

Job van Riet j.vanriet@erasmusmc.nl

See Also

Other RNA-Seq: importArriba(), retrieveDESeq2Results()

Examples

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	runArriba(
	  data.SV = DR71.CohortWGS$structuralVariants,
	  minTAF = 0.05,
	  bamFolder = '/mnt/data2/hartwig/DR71/Oct2020/dataHMF/RNASeq/BAM/',
	  outputFolder = '/mnt/data2/hartwig/DR71/Oct2020/dataHMF/RNASeq/Arriba/'
	)

J0bbie/R2CPCT documentation built on Feb. 24, 2022, 8:15 a.m.