evalTypeIError | R Documentation |
This function evaluates the type I error rate of selected methods for enrichment analysis when applied to one or more expression datasets.
evalTypeIError(
methods,
exp.list,
gs,
alpha = 0.05,
ea.perm = 1000,
tI.perm = 1000,
perm.block.size = -1,
summarize = TRUE,
save2file = FALSE,
out.dir = NULL,
verbose = TRUE,
...
)
methods |
Methods for enrichment analysis. This can be either
|
exp.list |
Experiment list. A |
gs |
Gene sets, i.e. a list of character vectors of gene IDs. |
alpha |
Numeric. Statistical significance level. Defaults to 0.05. |
ea.perm |
Integer. Number of permutations of the sample group assignments during enrichment analysis. Defaults to 1000. Can also be an integer vector matching the length of 'methods' to assign different numbers of permutations for different methods. |
tI.perm |
Integer. Number of permutations of the sample group assignments
during type I error rate evaluation. Defaults to 1000. Can also be an integer
vector matching the length of |
perm.block.size |
Integer. When running in parallel, splits |
summarize |
Logical. If |
save2file |
Logical. Should results be saved to file for subsequent
benchmarking? Defaults to |
out.dir |
Character. Determines the output directory where results are
saved to. Defaults to |
verbose |
Logical. Should progress be reported? Defaults to |
... |
Additional arguments passed to the selected enrichment methods. |
A list with an entry for each method applied. Each method entry is
a list with an entry for each dataset analyzed. Each dataset entry is either
a summary (summarize=TRUE
) or the full vector of type I error rates
(summarize=FALSE
) across tI.perm
permutations of the sample labels.
Ludwig Geistlinger <Ludwig.Geistlinger@sph.cuny.edu>
sbea
and nbea
for carrying out set- and network-based enrichment analysis.
BiocParallelParam
and register
for
configuration of parallel computation.
# loading three datasets from the GEO2KEGG compendium
geo2kegg <- loadEData("geo2kegg", nr.datasets=3)
# only considering the first 1000 probes for demonstration
geo2kegg <- lapply(geo2kegg, function(d) d[1:1000,])
# preprocessing and DE analysis for two of the datasets
geo2kegg <- maPreproc(geo2kegg[2:3])
geo2kegg <- runDE(geo2kegg)
# getting a subset of human KEGG gene sets
gs.file <- system.file("extdata", package="EnrichmentBrowser")
gs.file <- file.path(gs.file, "hsa_kegg_gs.gmt")
kegg.gs <- EnrichmentBrowser::getGenesets(gs.file)
# evaluating type I error rate of two methods on two datasets
# NOTE: using a small number of permutations for demonstration;
# for a meaningful evaluation tI.perm should be >= 1000
res <- evalTypeIError(geo2kegg, methods=c("ora",
"camera"), gs=kegg.gs, ea.perm=0, tI.perm=3)
# applying a user-defined enrichment method ...
# ... or a mix of pre-defined and user-defined methods
dummySBEA <- function(se, gs)
{
sig.ps <- sample(seq(0, 0.05, length=1000), 5)
nsig.ps <- sample(seq(0.1, 1, length=1000), length(gs)-5)
ps <- sample(c(sig.ps, nsig.ps), length(gs))
names(ps) <- names(gs)
return(ps)
}
methods <- list(camera = "camera", dummySBEA = dummySBEA)
res <- evalTypeIError(methods, geo2kegg, gs=kegg.gs, tI.perm=3)
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