# source("setupConfig.R")
# Set up run config: paths, name, organism
setupConfig <- function(pathRef, pathData, datasetName, organism, bPairedEnd, bOverwrite=TRUE)
{
config <- list()
# Path to reference fasta and gtf files; these will be copied locally
config$pathRef <- pathRef
# Path to input fastq files; these will be copied (or symlinked) locally
config$pathData <- pathData
# Path to aroma.seq package data
config$pathExData <- system.file("exData", package="aroma.seq")
# Dataset metadata
config$datasetName <- datasetName
config$organism <- organism
# config$bPairedEnd <- FALSE # [ Assign PE status later, at alignment stage ]
# config$qualityEncoding <- "illumina" # c("sanger", "solexa", "illumina"); cf. qrqc:ReadSeqFile
config$bPairedEnd <- bPairedEnd
config$bOverwrite <- bOverwrite
return(config)
}
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