context("fry")
test_that('fry runs equivalently from do.roast vs direct call', {
vm <- exampleExpressionSet()
gsi <- exampleGeneSets(vm)
gsl <- exampleGeneSets()
gsd <- conform(GeneSetDb(gsl), vm)
## We have to ensure that the genesets are tested in the same order as they
## are tested from the GeneSetDb for the pvalues to be equivalent given
## the same random seed.
gsd.idxs <- as.list(gsd, value='x.idx')
gsi <- gsi[names(gsd.idxs)]
fried <- limma::fry(vm, gsi, vm$design, ncol(vm$design), sort=FALSE)
my <- multiGSEA:::do.fry(gsd, vm, vm$design, ncol(vm$design))
expect_equal(my, fried, check.attributes=FALSE)
mgr <- multiGSEA:::mgres.fry(my, gsd)
gs.tuple <- split_gskey(rownames(my))
expect_equal(mgr$collection, gs.tuple$collection)
expect_equal(mgr$name, gs.tuple$name)
})
test_that("fry runs through multiGSEA wrapper", {
vm <- exampleExpressionSet()
gsi <- exampleGeneSets(vm)
gsl <- exampleGeneSets()
gsd <- conform(GeneSetDb(gsl), vm)
## We have to ensure that the genesets are tested in the same order as they
## are tested from the GeneSetDb for the pvalues to be equivalent given
## the same random seed.
gsd.idxs <- as.list(gsd, value='x.idx')
gsi <- gsi[names(gsd.idxs)]
fried <- limma::fry(vm, gsi, vm$design, ncol(vm$design), sort=FALSE)
my <- multiGSEA(gsd, vm, vm$design, ncol(vm$design), methods='fry')
mgres <- transform(result(my, 'fry'),
key=encode_gskey(collection, name),
stringsAsFactors=FALSE)
expect_true(setequal(rownames(fried), mgres$key))
comp <- fried[mgres$key,]
expect_equal(mgres$n, comp$NGenes)
expect_equal(mgres$pval, comp$PValue)
})
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