test_validCytoScan <- function(){
filePath <- system.file("extdata", "Affy_cytoScan.cyhd.CN5.CNCHP.txt.bz2",
package = "rCGH")
checkTrue(rCGH:::.validCytoScan(filePath))
}
test_validSNP6 <- function(){
filePath <- system.file("extdata", "Affy_snp6_cnchp.txt.bz2",
package = "rCGH")
checkTrue(rCGH:::.validSNP6(filePath))
}
test_validAgilent <- function(){
filePath <- system.file("extdata", "Agilent4x180K.txt.bz2",
package = "rCGH")
checkTrue(rCGH:::.validAgilent(filePath))
}
test_Cores <- function(){
rCGH:::.setCores(4, FALSE) == 4
}
test_ToFewCores <- function(){
rCGH:::.setCores(0, FALSE) == 1
}
test_ToManyCores <- function(){
rCGH:::.setCores(1e12, FALSE) == parallel:::detectCores()
}
test_NotNumCores <- function(){
checkException(rCGH:::.setCores("a", FALSE), silent = TRUE)
}
test_Segmentation <- function(){
L2R <- rnorm(1e3)
Chr <- rep(1:3, each = 1e3)
Chr[1e3] <- 4
Pos <- 1e3
checkException(rCGH:::.computeSegmentation(L2R, Chr, Pos, NA, NA, 1),
silent = TRUE)
}
test_setter <- function(){
filePath <- system.file("extdata", "Affy_cytoScan.cyhd.CN5.CNCHP.txt.bz2",
package = "rCGH")
cgh <- readAffyCytoScan(filePath, sampleName = "AffyScHD")
setInfo(cgh, "item1") <- 35
setInfo(cgh, "item2") <- TRUE
checkTrue(
getInfo(cgh, "item1") == 35 &&
getInfo(cgh, "item2") == TRUE &&
checkException(setInfo(cgh) <- "whatever", silent = TRUE) &&
checkException(setInfo(cgh, "whatever"), silent = TRUE)
)
}
test_getter <- function(){
filePath <- system.file("extdata", "Affy_cytoScan.cyhd.CN5.CNCHP.txt.bz2",
package = "rCGH")
cgh <- readAffyCytoScan(filePath, sampleName = "AffyScHD")
checkTrue(
getInfo(cgh, "fileName") == "Affy_cytoScan.cyhd.CN5.CNCHP.txt.bz2" &&
getInfo(cgh, "sampleName") == "AffyScHD" &&
getInfo(cgh, "analysisDate") == format(Sys.Date(), "%Y-%m-%d") &&
getInfo(cgh, "rCGH_version") == as.character(packageVersion("rCGH"))
)
}
test_Pipeline <- function(){
# Reading
filePath <- system.file("extdata", "Affy_cytoScan.cyhd.CN5.CNCHP.txt.bz2",
package = "rCGH")
cgh <- readAffyCytoScan(filePath, sampleName = "sample1", labName = "myLab")
if(!checkTrue(inherits(cgh, "rCGH")))
stop("Error when reading Affy_cytoScan")
# Adjusting
cgh <- adjustSignal(cgh, nCores=1)
pars <- getParam(cgh)
if(length(pars)<10)
stop("Error when Adjusting: too few parameters.")
if(is.null(pars$dLRs))
stop("Error when Adjusting: dLRs is missing.")
if(is.null(pars$MAD))
stop("Error when Adjusting: MAD is missing.")
# Segmenting
cgh <- segmentCGH(cgh, nCores=1)
pars <- getParam(cgh)
st <- getSegTable(cgh)
if(is.null(pars$nSegment))
stop("Error when segmenting: nSegment is missing.")
if(nrow(st)==0)
stop("Error when segmenting: empty segmentation table.")
# Centering
cgh <- EMnormalize(cgh)
pars <- getParam(cgh)
if(length(pars)<18)
stop("Error when centralizing: too few parameters.")
if(is.null(pars$nPeak))
stop("Error when centralizing: nPeak is missing.")
if(is.null(pars$correctionValue))
stop("Error when centralizing: correctionValue is missing.")
# Extracting genes
bg <- byGeneTable(st)
if(nrow(bg)==0)
stop("Error when extracting genes: empty gene table.")
# Plotting profile
p <- plotProfile(cgh)
if(is.null(p))
stop("Error when plotting profile.")
# Plotting LOH
p <- plotLOH(cgh)
if(is.null(p))
stop("Error when plotting LOH.")
TRUE
}
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