Visualizes the interaction between a facet and a grouping variable as a heatmap. Rows represent facet levels, columns represent group values, and cell color indicates the selected metric.
Usage
plot_dif_heatmap(
x,
metric = c("obs_exp", "t", "contrast"),
draw = TRUE,
show_values = TRUE,
value_digits = 2L,
flag_threshold = NULL,
scale_limit = NULL,
flag_color = "black",
...
)Arguments
- x
Output from
dif_interaction_table(),analyze_dff(), oranalyze_dif(). When anmfrm_dff/mfrm_difobject is passed, thecell_tableelement is used (requiresmethod = "residual").- metric
Which metric to plot:
"obs_exp"for observed-minus-expected average (default),"t"for the standardized residual / t-statistic, or"contrast"for pairwise differential-functioning contrast (only formfrm_dffobjects withdif_table).- draw
If
TRUE(default), draw the plot.- show_values
Logical. If
TRUE(default), print rounded cell values on top of the heatmap.- value_digits
Non-negative integer number of digits after the decimal point for cell labels.
- flag_threshold
Optional non-negative absolute-value threshold. When supplied, cells with
abs(value) >= flag_thresholdare recorded in$data$flag_matrixand outlined on the drawn heatmap.- scale_limit
Optional positive scalar for a symmetric color scale from
-scale_limitto+scale_limit. Use this to make several heatmaps visually comparable.- flag_color
Border color for cells meeting
flag_threshold.- ...
Additional graphical parameters passed to
graphics::image().
Value
Invisibly, an mfrm_plot_data object whose data slot bundles
the row x column metric matrix ($matrix), the source long table
($pairs), and the metric label. Earlier 0.1.x releases returned the
bare matrix; consume $data$matrix to keep code forward-compatible.
Interpreting output
Warm colors (red) indicate positive Obs-Exp values (the model underestimates the facet level for that group).
Cool colors (blue) indicate negative Obs-Exp values (the model overestimates).
White/neutral indicates no systematic difference.
The
"contrast"view is best for pairwise differential-functioning summaries, whereas"obs_exp"and"t"are best for cell-level diagnostics.
Typical workflow
Compute interaction with
dif_interaction_table()or differential- functioning contrasts withanalyze_dff().Plot with
plot_dif_heatmap(...).Identify extreme cells or contrasts for follow-up.
Examples
if (FALSE) { # interactive()
toy <- load_mfrmr_data("example_bias")
fit <- fit_mfrm(toy, "Person", c("Rater", "Criterion"), "Score",
method = "JML", model = "RSM", maxit = 30)
diag <- diagnose_mfrm(fit, residual_pca = "none")
int <- dif_interaction_table(fit, diag, facet = "Rater",
group = "Group", data = toy, min_obs = 2)
heat <- plot_dif_heatmap(int, metric = "obs_exp", draw = FALSE)
dim(heat$data$matrix)
# Look for (`metric = "obs_exp"`): cells near 0 are aligned with
# model expectation; |Obs - Exp| > 0.5 logits is a substantive
# gap. With `metric = "t"` the cell scale becomes a standardized
# residual where |t| > 2 is a screening flag, not a standalone
# hypothesis test. With `metric = "contrast"` the layout switches
# to Level x GroupPair and reads as the pairwise differential-
# functioning contrast (use `analyze_dff()`).
}