The hardware and bandwidth for this mirror is donated by dogado GmbH, the Webhosting and Full Service-Cloud Provider. Check out our Wordpress Tutorial.
If you wish to report a bug, or if you are interested in having us mirror your free-software or open-source project, please feel free to contact us at mirror[@]dogado.de.
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.
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")Use the Wright map first when you want one shared logit view of persons, facet levels, and step thresholds.
Interpretation:
Next, use the pathway map when you want to see how expected scores progress across theta.
Interpretation:
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:
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:
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:
For a compact visual workflow:
plot_qc_dashboard() for one-page triage.plot_unexpected(), plot_displacement(),
and plot_interrater_agreement() for local follow-up.plot(fit, type = "wright") and
plot(fit, type = "pathway") for targeting and scale
interpretation.plot_residual_pca() and
plot_bias_interaction() for deeper structural review.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.