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mfrmr Visual Diagnostics

This vignette is a compact map of the main base-R diagnostics in mfrmr. It is organized around four practical questions:

All examples use packaged data and preset = "publication" so the same code is suitable for manuscript-oriented graphics.

Minimal setup

library(mfrmr)

toy <- load_mfrmr_data("example_core")

fit <- fit_mfrm(
  toy,
  person = "Person",
  facets = c("Rater", "Criterion"),
  score = "Score",
  method = "JML",
  model = "RSM",
  maxit = 20
)
#> Warning: Optimizer did not fully converge (code = 1). Consider increasing maxit
#> (current: 20) or relaxing reltol (current: 1e-06).

diag <- diagnose_mfrm(fit, residual_pca = "none")

1. Targeting and scale structure

Use the Wright map first when you want one shared logit view of persons, facet levels, and step thresholds.

plot(fit, type = "wright", preset = "publication", show_ci = TRUE)

Interpretation:

Next, use the pathway map when you want to see how expected scores progress across theta.

plot(fit, type = "pathway", preset = "publication")

Interpretation:

2. Local response and level issues

Unexpected-response screening is useful for case-level review.

plot_unexpected(
  fit,
  diagnostics = diag,
  abs_z_min = 1.5,
  prob_max = 0.4,
  plot_type = "scatter",
  preset = "publication"
)

Interpretation:

Displacement focuses on level movement rather than individual responses.

plot_displacement(
  fit,
  diagnostics = diag,
  anchored_only = FALSE,
  plot_type = "lollipop",
  preset = "publication"
)

Interpretation:

3. Linking and coverage

When the design may be incomplete or spread across subsets, inspect the coverage matrix before interpreting cross-subset contrasts.

sc <- subset_connectivity_report(fit, diagnostics = diag)
plot(sc, type = "design_matrix", preset = "publication")

Interpretation:

If you are working across administrations, follow up with anchor-drift plots:

drift <- detect_anchor_drift(current_fit, baseline = baseline_anchors)
plot_anchor_drift(drift, type = "heatmap", preset = "publication")

4. Residual structure and interaction screens

Residual PCA is a follow-up layer after the main fit screen.

diag_pca <- diagnose_mfrm(fit, residual_pca = "both", pca_max_factors = 4)
pca <- analyze_residual_pca(diag_pca, mode = "both")
plot_residual_pca(pca, mode = "overall", plot_type = "scree", preset = "publication")

Interpretation:

For interaction screening, use the packaged bias example.

bias_df <- load_mfrmr_data("example_bias")

fit_bias <- fit_mfrm(
  bias_df,
  person = "Person",
  facets = c("Rater", "Criterion"),
  score = "Score",
  method = "MML",
  model = "RSM",
  quad_points = 7
)

diag_bias <- diagnose_mfrm(fit_bias, residual_pca = "none")
bias <- estimate_bias(fit_bias, diag_bias, facet_a = "Rater", facet_b = "Criterion")

plot_bias_interaction(
  bias,
  plot = "facet_profile",
  preset = "publication"
)

Interpretation:

These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.