| plotPValues {DRIMSeq} | R Documentation |
Plot p-value distribution
plotPValues(x, ...) ## S4 method for signature 'dmDStest' plotPValues(x, level = "gene") ## S4 method for signature 'dmSQTLtest' plotPValues(x)
x |
|
... |
Other parameters that can be defined by methods using this generic. |
level |
Character specifying which type of results to return. Possible
values |
Plot a histogram of p-values.
Malgorzata Nowicka
plotData, plotPrecision,
plotProportions
# --------------------------------------------------------------------------
# Create dmDSdata object
# --------------------------------------------------------------------------
## Get kallisto transcript counts from the 'PasillaTranscriptExpr' package
library(PasillaTranscriptExpr)
data_dir <- system.file("extdata", package = "PasillaTranscriptExpr")
## Load metadata
pasilla_metadata <- read.table(file.path(data_dir, "metadata.txt"),
header = TRUE, as.is = TRUE)
## Load counts
pasilla_counts <- read.table(file.path(data_dir, "counts.txt"),
header = TRUE, as.is = TRUE)
## Create a pasilla_samples data frame
pasilla_samples <- data.frame(sample_id = pasilla_metadata$SampleName,
group = pasilla_metadata$condition)
levels(pasilla_samples$group)
## Create a dmDSdata object
d <- dmDSdata(counts = pasilla_counts, samples = pasilla_samples)
## Use a subset of genes, which is defined in the following file
gene_id_subset <- readLines(file.path(data_dir, "gene_id_subset.txt"))
d <- d[names(d) %in% gene_id_subset, ]
# --------------------------------------------------------------------------
# Differential transcript usage analysis - simple two group comparison
# --------------------------------------------------------------------------
## Filtering
## Check what is the minimal number of replicates per condition
table(samples(d)$group)
d <- dmFilter(d, min_samps_gene_expr = 7, min_samps_feature_expr = 3,
min_gene_expr = 10, min_feature_expr = 10)
plotData(d)
## Create the design matrix
design_full <- model.matrix(~ group, data = samples(d))
## To make the analysis reproducible
set.seed(123)
## Calculate precision
d <- dmPrecision(d, design = design_full)
plotPrecision(d)
head(mean_expression(d))
common_precision(d)
head(genewise_precision(d))
## Fit full model proportions
d <- dmFit(d, design = design_full)
## Get fitted proportions
head(proportions(d))
## Get the DM regression coefficients (gene-level)
head(coefficients(d))
## Get the BB regression coefficients (feature-level)
head(coefficients(d), level = "feature")
## Fit null model proportions and perform the LR test to detect DTU
d <- dmTest(d, coef = "groupKD")
## Plot the gene-level p-values
plotPValues(d)
## Get the gene-level results
head(results(d))
## Plot feature proportions for a top DTU gene
res <- results(d)
res <- res[order(res$pvalue, decreasing = FALSE), ]
top_gene_id <- res$gene_id[1]
plotProportions(d, gene_id = top_gene_id, group_variable = "group")
plotProportions(d, gene_id = top_gene_id, group_variable = "group",
plot_type = "lineplot")
plotProportions(d, gene_id = top_gene_id, group_variable = "group",
plot_type = "ribbonplot")