repicc | R Documentation |
The function can be used to calculate ICC for each CpG probe using balanced or unbalanced replicate samples.
repicc(dat,repid,mvalue=FALSE,nCores=2,qcflag=FALSE,qc=NULL,
detPthre=0.05,nbthre=3)
dat |
Methylation beta value matrix |
repid |
A data frame with two variables, id and idx. id should be the same with column name of "dat", idx is a variable to show the relationship between samples with same value for samples from same individual. |
mvalue |
If TRUE, the beta value will be converted to M value for calculation of ICC |
nCores |
Number of cores will be used for calculation of ICC |
qcflag |
Whether to perform QC before calculation of ICC |
qc |
QC object from function QCinfo |
detPthre |
If qcflag=TRUE, the methylation values with detection P value higher than the threshold will be removed before calculation |
nbthre |
If qcflag=TRUE, the methylation values with number of bead smaller |
A data frame containing ICC for each probe
Zongli Xu
Zongli Xu, Jack A Taylor. Reliability of DNA methylation measures using Illumina methylation BeadChip. Epigenetics 2020
if (require(minfiData)){
path <- file.path(find.package("minfiData"),"extdata")
rgSet <- readidat(path = path,recursive = TRUE)
mdat=getmeth(rgSet)
beta=getB(mdat,"Illumina")
repid=data.frame(id=c("5723646052_R02C02","5723646052_R04C01","5723646052_R05C02","5723646053_R04C02","5723646053_R05C02","5723646053_R06C02"),idx=c(1,2,3,1,2,3))
iccresu<-repicc(dat=beta,repid=repid)
}
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