library(DRomics) visualize <- FALSE # put to TRUE for a manual check of plots doboot <- FALSE if(visualize) { # Impact of ratio2switchinlog and minBMD on a toy example # # datafilename <- system.file("extdata", "transcripto_very_small_sample.txt", package="DRomics") datafilename <- system.file("extdata", "transcripto_sample.txt", package="DRomics") (o <- microarraydata(datafilename, check = TRUE, norm.method = "cyclicloess")) (s_quad <- itemselect(o, select.method = "quadratic", FDR = 0.01)) (f <- drcfit(s_quad, progressbar = TRUE)) (r <- bmdcalc(f)) plot(r) r$res (r <- bmdcalc(f, ratio2switchinlog = 1)) plot(r) (r <- bmdcalc(f, minBMD = 2)) plot(r) (r <- bmdcalc(f, minBMD = 2, ratio2switchinlog = 1)) plot(r) # check of defensive prog # (r <- bmdcalc(f, minBMD = 0)) # (r <- bmdcalc(f, minBMD = 1)) # 1 > minimal non null dose # look at BMR in the output (r <- bmdcalc(f, z = 2, x = 20)) r$res r$minBMD # bootstrap after forcing minBMD to a high value # without anay interest, but just to test bmdboot (r <- bmdcalc(f, minBMD = 2)) (b <- bmdboot(r, niter = 100)) # with a non reasonable value for niter b$res plot(b) # plot of BMD.zSD after removing of BMDs with infinite upper bounds # and with minBMD to its default value (dosemin/100) (r <- bmdcalc(f)) (b <- bmdboot(r, niter = 100)) # with a non reasonable value for niter plot(b) # plot of BMD.zSD after removing of BMDs with infinite upper bounds # using an RNAseq example # subsample # datafilename <- system.file("extdata", "RNAseq_sample.txt", package="DRomics") # (o <- RNAseqdata(datafilename, check = TRUE, transfo.method = "vst")) # whole data data(Zhou_kidney_pce) d <- Zhou_kidney_pce (o <- RNAseqdata(d)) (s <- itemselect(o, select.method = "quadratic", FDR = 0.01)) (f <- drcfit(s, progressbar = TRUE)) head(f$fitres) (r <- bmdcalc(f)) plot(r) (r <- bmdcalc(f, ratio2switchinlog = 1)) plot(r) (r <- bmdcalc(f, minBMD = 0.0001, ratio2switchinlog = 1)) plot(r) (r <- bmdcalc(f, minBMD = 1)) plot(r) }