RNA-Seq in baySeq - how to interpret a result
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6.9 years ago
iza08.ik ▴ 20

Hello,

I need help.

I wrote and used the code:

groups <- list(NDE = c(1,1), DE = c(2,1)) replicates <- c('adipose','brain') CD <- new("countData", data = as.matrix(wang22)[1:1000,6:7], replicates = replicates, groups = groups) libsizes(CD) <- getLibsizes(CD, estimationType = "quantile") plotMA.CD(CD, samplesA = 'adipose', samplesB = 'brain', col = c(rep("red", 100), rep("black", 900))) if(require("parallel")) cl <- makeCluster(8) else cl <- NULL CD <- getPriors.NB(CD, samplesize = 10000, estimation = "QL", cl = cl) CD <- getLikelihoods(CD, cl = cl, bootStraps = 3, verbose = FALSE) topCounts(CD, group = "DE")

I don't know how to interpret the result and which gene are different expressed.

Can you help me, please?

RNA-Seq baySeq R Bioconductor • 1.2k views
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