| diagnose | R Documentation |
Reports genuine ranger edge-specific OOB concordance. Optionally, complete patient-level cross-validation refits every edge forest and returns IPCW full-state Brier scores and an integrated Brier score.
diagnose(object, ...)
## S3 method for class 'rfmstate'
diagnose(
object,
eval_times = NULL,
method = c("edge_oob", "cv"),
folds = 5L,
repeats = 1L,
seed = 2026L,
g_min = 0.05,
...
)
object |
A fitted |
... |
Ignored; validation settings must use the documented arguments. |
eval_times |
Prespecified calendar-time validation horizons. For
|
method |
|
folds |
Positive integer number of patient-level folds for cross-validation. |
repeats |
Positive integer number of repeated fold assignments. |
seed |
Nonnegative integer fold-assignment and refit seed. |
g_min |
Minimum allowed training-fold censoring survival, strictly between zero and one. |
Ranger OOB concordance is 1 - prediction.error for each
binary cause-specific edge endpoint. It does not validate the assembled
multistate probability vector. Full-state scores use subject-level held-out
predictions and training-fold Kaplan–Meier censoring estimates. The
stronger marginal independent-censoring assumption applies to these KM
weights. Fold assignment occurs before schema construction; unordered
factor levels and numeric ranges are reconstructed from training subjects
only. A held-out-only factor level is an explicit fold failure. No
bias–variance decomposition is provided.
An rfmstate_diag object. Edge OOB tables
(edge_oob, oob_error, and concordance) are always
present. With cross-validation, brier is a full-state IPCW score
table, ibs is its trapezoidal integral over
integration_interval, and fold assignments/support/seeds are stored
in assignments and fold_summary; folds is a
backward-compatible alias for fold_summary. The object also records
evaluation times, whether their grid was prespecified or exploratory,
censoring model, g_min, method, and an explicit validation label.
Edge OOB concordance applies only to separate binary cause-specific
endpoints and is not a full-pipeline validation score. Cross-validation
currently uses a training-fold marginal Kaplan–Meier censoring model and
therefore requires marginal independent censoring for the score. Every fold
must fit every declared edge and cover all evaluation horizons; failures,
sparse edges, or censoring survival below g_min stop validation. No
calibration model, prediction interval, or bias–variance decomposition is
returned. Automatically generated evaluation times are exploratory and are
labeled as such; confirmatory work should supply prespecified times.
ms <- clinical_states()
dat <- sim_clinical_data(300, structure = ms, seed = 42)
long <- prepare_data(
dat, "ID", ms,
list(Responded="time_Responded", Unresponded="time_Unresponded",
Stabilized="time_Stabilized", Progressed="time_Progressed",
Death="time_Death"),
"time_censored", c("age", "sex", "BMI", "treatment")
)
fit <- rfmstate(long, num.trees = 100, min_events = 3, seed = 42)
diagnose(fit)
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