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prefiltering isotopically labeled analytes according to the experiment design.
prefilter(xset, subgroup = NULL, unlabel = NULL, reps = TRUE, p = 0.05, folds = 10)
xcms object.
subset the xcms groups. The name should be the same as in phboData$class. default = NULL, which means no subset will be performed.
specify which is unlabeled group.
if there are replicates in the sample.
p-value threshold, default value = 0.05
fold change threshold, default value = 10
a filtered peaklist
# NOT RUN { data(lcms) explist <- prefilter(lcms, subgroup = c("B", "C", "D"), unlabel = "B") # }
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