test_that("range_beta_values", {
ssEnv <- init_env(tempFolder, parallel_strategy = "sequential")
nitem <- 1e4
nsamples <- 21
probe_features <- PROBES_Gene_Whole[!is.na(PROBES_Gene_Whole$START),c("CHR","START","PROBE")]
probe_features <- unique(probe_features)
probe_features$END <- probe_features$START
nitem <- min(nitem, nrow(probe_features))
probe_features <- probe_features[probe_features$PROBE %in% sample(x=probe_features[,"PROBE"] , size=nitem),]
methylation_data <- rnorm(nitem*nsamples,mean = 0.5, sd = 0.7)
methylation_data <- as.data.frame(matrix(methylation_data,nitem,nsamples))
row.names(methylation_data) <- probe_features$PROBE
# Sample_ID <- stri_rand_strings(nsamples, 15, pattern = "[A-Za-z]")
# colnames(methylation_data) <- Sample_ID
# Sample_Group <- c(rep("Control",nsamples/3),rep("Case",nsamples/3),rep("Reference",nsamples/3))
# sample_sheet <- data.frame(Sample_Group, Sample_ID)
#
# sliding_window_size <- 11
# bonferroni_threshold <- 0.01
# batch_id <- 1
iqrTimes <- 3
rr <- range_beta_values(methylation_data)
# sp <- analyze_batch(
# methylation_data = methylation_data,
# sample_sheet = sample_sheet,
# sliding_window_size = sliding_window_size,
# bonferroni_threshold = bonferroni_threshold,
# iqrTimes = iqrTimes,
# batch_id = batch_id)
#
# message(nrow(sp))
# message(nrow(sample_sheet))
testthat::expect_true(sum(colnames(rr)==c("beta_inferior_thresholds","beta_superior_thresholds","beta_median_values"))==3)
testthat::expect_true(nrow(rr)==nrow(methylation_data))
testthat::expect_true(rr$beta_inferior_thresholds[1]!=rr$beta_superior_thresholds[1])
testthat::expect_true(rr$beta_inferior_thresholds[1]!=rr$beta_median_values[1])
# future::plan( future::multisession)
})
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