Channel splitting problem
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@krasikovscienceuvanl-1517
Last seen 9.6 years ago
Hello, I have a strange problem occured in spliting two-channel data into single channel set The funny story is that the same code (adopted from limma user's guide) works well for another set of microarrays. All the differencies between two sets are first one is 8K Custom Agilent and second one is 11K Custom Agilent. Both of them contains the same number of Probes (8091), but different number of Control spots. As well probe annotation is slightly different. probeNames are the same and unique on both arrays, but corresponding geneNames are different. Most geneNames are missing in 8K microarray, whereas on 11K there are no missing values. Maybe that is the reason for below described failure. Has anybody any suggestions how to solve it? # The Code: >targets <- readTargets(file=targetsFile, path=loadPath, sep="\t") >RG <- read.maimages(targets$fileName, path=loadPath, source="agilent", quote="") # SpotTypes attachement: >spottypes <- readSpotTypes(file = "SpotTypeFile.txt", path = "qqq") >show(spottypes) >RG$genes$Status <- controlStatus(spottypes, RG) # Removing Control spots: >isGene <- RG$genes$Status == "Gene" >RGc <- RG[isGene,] # Normalization: >RGb <- backgroundCorrect(RGc,method="minimum") >MAlo <- normalizeWithinArrays(RGb, method="loess") >MAaq <- normalizeBetweenArrays(MAlo, method="Aquantile") # Channel Spliting: >targets2 <- targetsA2C(targets) >u <- unique(targets2$Target) >f <- factor(targets2$Target, levels=u) >design <- model.matrix(~0+f) >colnames(design) <- u >corfit <- intraspotCorrelation(MAaq, design) Here I'm getting long list of the same "Warning message: NaNs produced in: log(x)" And then lmscfit doesn't work: >fit <- lmscFit(MAaq, design, correlation=corfit$consensus) "Error in if (abs(correlation) >= 1) stop("correlation must be strictly between -1 and 1") : missing value where TRUE/FALSE needed" Any suggestions? Best wishes Vladimir
Microarray Annotation probe limma Microarray Annotation probe limma • 908 views
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