Open ekarlins opened 7 years ago
I'm going to create a new branch named after this issue to start implementing this plan, wrapped with snakemake:
read in the idat files using R "illuminaio". I'll generalize the code below:
RedIdatIntensityMatrix <- function(path){ require(illuminaio) redIdats <- dir(path, pattern = "_Red.idat") red1 <- readIDAT(paste(path, redIdats[1], sep = "/")) m <- cbind(red1$Quants[,1]) for (i in 2:length(redIdats)){ redI <- redIdats[i] red <- readIDAT(paste(path, redI, sep = "/")) m <- cbind(m, red$Quants[,1]) } m }
Run quantile normalization, one channel at a time (Red and Grn) and split into sub-bead pools, as described in this document: http://dnatech.genomecenter.ucdavis.edu/wp-content/uploads/2013/06/illumina_gt_normalization.pdf
The sub-bead pool ID is in the manifest as "BeadSetID".
I need to generalize the code below and take it to LRR and BAF calculations and write to file.
quantile normalization:
require(preprocessCore) r <- RedIdatIntensityMatrix(path) probesToKeep <- annotation$AddressA_ID[annotation$BeadSetID == myBeadID] newR <- r[as.character(probesToKeep),] newNormR <- normalize.quantiles(newR)
I'm going to create a new branch named after this issue to start implementing this plan, wrapped with snakemake:
read in the idat files using R "illuminaio". I'll generalize the code below:
Run quantile normalization, one channel at a time (Red and Grn) and split into sub-bead pools, as described in this document: http://dnatech.genomecenter.ucdavis.edu/wp-content/uploads/2013/06/illumina_gt_normalization.pdf
The sub-bead pool ID is in the manifest as "BeadSetID".
I need to generalize the code below and take it to LRR and BAF calculations and write to file.
quantile normalization: