context("Annotations parameters")
## Object cc will be used in units below. Querying error-prone biomart only
## once.
library("pRolocdata")
data("hyperLOPIT2015")
hyperLOPIT2015 <- markerMSnSet(hyperLOPIT2015)
par <- setAnnotationParams(inputs = c("Mouse genes",
"UniProtKB/Swiss-Prot ID"))
cc <- addGoAnnotations(hyperLOPIT2015, par,
namespace = "cellular_component")
test_that("Used annotation params successfully", {
expect_true(validObject(cc))
})
context("GO annotations framework")
test_that("filtering by min or max matrix annotations gives expected results", {
## Check that min markers specified matches output
m1 <- 20
cc1 <- filterMinMarkers(cc, n = m1)
m2 <- min(colSums(fData(cc1)$GOAnnotations))
expect_true(m1 <= m2)
## Check that max markers specified matches output
m1 <- 50
cc2 <- filterMaxMarkers(cc, n = m1)
m2 <- max(colSums(fData(cc2)$GOAnnotations))
expect_true(m1 >= m2)
})
context("clustDist function")
test_that("output from orderGoAnnotations and manually ordering clusters", {
seed <- sample(.Machine$integer.max, 1)
cc <- filterMinMarkers(cc, n = 20)
cc <- filterMaxMarkers(cc, p = .5)
res <- orderGoAnnotations(cc, k = 1:3, p = 1/3,
verbose = FALSE, seed = seed)
orgs1 <- colnames(fData(res)$GOAnnotations)
## Manually calculate distance and re-order by min
dd <- clustDist(cc, fcol = "GOAnnotations", k = 1:3,
verbose = FALSE, seed = seed)
minDist <- getNormDist(dd, p = 1/3)
o <- order(minDist)
orgs2 <- names(dd)[o]
expect_equal(orgs1, orgs2)
})
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