data(enterotypes_arumugam)
enterotype <- phyloseq::subset_samples(
enterotypes_arumugam,
Enterotype %in% c("Enterotype 3", "Enterotype 2", "Enterotype 1")
)
tukey_res <- run_posthoc_test(enterotype, "Enterotype", method = "tukey")
test_that("etaseq effect size", {
etasq <- calc_etasq(c(1, 2, 1.2, 3, 4, 1.4), c("a", "b", "c", "a", "b", "c"))
expect_equal(signif(etasq, 3), 0.421)
})
test_that("test multiple group enterotype result", {
# error group
expect_error(
run_test_multiple_groups(enterotype, "Entertype"),
regexp = "`group` must in the field of sample meta data",
fixed = TRUE
)
})
test_that("test post hoc test result", {
res_test <- tukey_res@result[["p__Bacteroidetes|g__Bacteroides"]] %>%
data.frame
expect_snapshot(print(res_test, digits = 5))
})
test_that("test visualization of post hoc test, p value significance level ", {
expect_equal(
pvalue2siglevel(c(0.05, 0.01, 0.0001, 0.06)),
c("*", "**", "***", "NS.")
)
})
test_that(
"test visualization of posthoc test, data of signicance level annotation",
{
# single feature
abd <- tukey_res@abundance
group <- abd$group
pht_df <- data.frame(tukey_res@result[["p__Bacteroidetes|g__Bacteroides"]])
annotation_single <- get_sig_annotation_single(
abd[["p__Bacteroidetes|g__Bacteroides"]],
pht_df,
group
)
annotation_single$y_position <- formatC(
annotation_single$y_position,
format = "g",
digits = 5
)
expect_snapshot(annotation_single)
# all features
annotation_all <- get_sig_annotation(tukey_res)
annotation_all$y_position <- formatC(
annotation_all$y_position,
format = "g",
digits = 5
)
expect_snapshot(head(annotation_all))
}
)
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