Plot a gg_partial_varpro object
Source: R/plot.gg_partial.R, R/plot.gg_partial_varpro.R
plot.gg_partial_varpro.RdDraws the partial dependence curves from the list that
gg_partial_varpro returns. Continuous predictors get
overlaid line curves, one per effect type; categorical predictors get
side-by-side boxplots. Survival path-C objects (the ones you get when
scale %in% c("surv","chf") was passed to the extractor) are
handed off to plot.gg_partial_rfsrc for drawing.
Arguments
- x
A
gg_partial_varproobject.- type
Character vector; one or more of
"parametric","nonparametric","causal". Defaults to all three. Ignored for path-C objects.- ...
Unused for path-A objects; forwarded to
plot.gg_partial_rfsrcfor path-C objects.
Details
Ensemble mortality (scale = "mortality"): when the provenance scale
is "mortality", the y-axis is labeled
"Ensemble mortality (expected events)". The wording is
deliberate: this is an unbounded relative-risk score, not a
survival probability and not \(1 - S(t)\) (Ishwaran, Kogalur,
Blackstone & Lauer, 2008 doi:10.1214/08-AOAS169).
Reading the partial dependence
For a continuous variable the x-axis is the variable's grid of values
and the y-axis is the partial prediction; each of the three effect
types (parametric, nonparametric, causal) is
drawn as its own line. The shape of the line is the story: a clear
slope says the model uses the variable, a flat line says it
essentially does not, and a U-shape or a threshold says the effect
is nonlinear in a way a single coefficient would miss. For a
categorical variable the picture is a boxplot per level; here the
eye is looking at level-to-level shifts in the center of each box.
Where the three effect types track each other, the parametric story is a fair summary of what the forest is doing. Where they fan apart (typically the parametric curve smoother than the nonparametric, or the causal curve flatter than either) the variable is one to inspect more carefully before reading a single effect off the plot.
What this tells you
Use these curves to describe how the model uses each variable, not
to claim how the world works. They are a window into the fitted
relationship; they do not by themselves establish that intervening
on the variable would move the outcome. For survival path-C
(scale = "chf"), the y-axis is on the cumulative-hazard scale.
Reading a probability curve (scale = "prob")
The y-axis is \(P(Y = \mathrm{target})\), the model's predicted probability
of the target class as the focal variable varies (others held at their
UVT-plausible average). "odds" and "logodds" are the same
curve on the odds and log-odds scales. The causal curve is a
contrast (below) and is not shown on "prob"/"odds";
use "logodds" to see it.
Reading a survival-probability curve (scale = "surv")
The y-axis is \(S(\tau \mid x)\), the predicted probability of surviving past \(\tau\), bounded in \([0, 1]\) and read in the model's time units. Higher is better (more survival). \(\tau\) defaults to the median follow-up time when not supplied.
What the causal curve is, and when to use it
causal is the baseline-subtracted local effect – varPro's
virtual- ("digital-") twins estimator (Ishwaran & Blackstone, 2025). It
shows how the prediction shifts as the focal variable moves away from the
reference grid point, with the other covariates held at on-manifold
(UVT-plausible) values; it is a contrast (it starts at 0), not a
level. Use it when you want the local effect (change-from-baseline) rather
than the absolute predicted level, and as a cross-check on the parametric
and nonparametric curves. It is varpro's local estimator within the
fitted model, not a structural causal claim about the
data-generating process. Because it is a contrast it cannot share a
probability/odds axis with the absolute curves, so it is shown only on the
additive scales ("logodds", "mortality", "rmst").
Reading an RMST curve (scale = "rmst")
The y-axis is restricted mean survival time at horizon \(\tau\), \(\mathrm{RMST}(\tau)=\int_0^\tau S(t)\,dt\): the expected event-free time during the first \(\tau\) time-units, the area under the survival curve out to \(\tau\). Read it in the model's own time units, where it is bounded by \(0 \le \mathrm{RMST}(\tau) \le \tau\).
Two things follow. First, \(\tau\) must be given in the fit's time units; a \(\tau\) past the largest event time just truncates to the full restricted mean and stops changing. Second, higher is better here – more time event-free – which is the opposite of the ensemble-mortality scale.
A continuous variable's curve sloping up means higher values of that covariate buy you more restricted-mean event-free time within \(\tau\) (with the other covariates held at their UVT-plausible average); a flat curve means the covariate does not move it. Unlike ensemble mortality, RMST reads on a directly clinical scale, "so many event-free time-units within \(\tau\)", which is usually the one you want to report.
References
Ishwaran H, Kogalur UB, Blackstone EH, Lauer MS (2008). Random survival forests. The Annals of Applied Statistics, 2(3), 841–860. doi:10.1214/08-AOAS169 .
Ishwaran H, Blackstone EH (2025). Harnessing the power of virtual (digital) twins: Graphical causal tools for understanding patient and hospital differences. Computational and Structural Biotechnology Journal, 28, 312.
Examples
set.seed(42)
n_obs <- 30; n_pts <- 15
mock_data <- list(
age = list(
xvirtual = seq(30, 80, length.out = n_pts),
xorg = sample(seq(30, 80, by = 5), n_obs, replace = TRUE),
yhat.par = matrix(rnorm(n_obs * n_pts), nrow = n_obs),
yhat.nonpar = matrix(rnorm(n_obs * n_pts), nrow = n_obs),
yhat.causal = matrix(rnorm(n_obs * n_pts), nrow = n_obs)
),
sex = list(
xvirtual = c(0, 1),
xorg = sample(c(0, 1), n_obs, replace = TRUE),
yhat.par = matrix(rnorm(n_obs * 2), nrow = n_obs),
yhat.nonpar = matrix(rnorm(n_obs * 2), nrow = n_obs),
yhat.causal = matrix(rnorm(n_obs * 2), nrow = n_obs)
)
)
pp <- gg_partial_varpro(mock_data)
plot(pp)
plot(pp, type = "parametric")