Estimating ANOVA Models with rstanarm
Jonah Gabry and Ben Goodrich
2026-03-09
Source:vignettes/aov.Rmd
aov.RmdIntroduction
This vignette explains how to estimate ANalysis Of VAriance (ANOVA)
models using the stan_aov function in the
rstanarm package
Steps 3 and 4 are covered in more depth by the vignette entitled “How to Use the rstanarm Package”. This vignette focuses on Step 1 when the likelihood is the product of independent normal distributions. We also demonstrate that Step 2 is not entirely automatic because it is sometimes necessary to specify some additional tuning parameters in order to obtain optimally efficient results.
Likelihood
The likelihood for one observation under a linear model can be written as a conditionally normal PDF where is a linear predictor and is the standard deviation of the error in predicting the outcome, . The likelihood of the entire sample is the product of individual likelihood contributions.
An ANOVA model can be considered a special case of the above linear regression model where each of the predictors in is a dummy variable indicating membership in a group. An equivalent linear predictor can be written as , which expresses the conditional expectation of the outcome in the -th group as the sum of a common mean, , and a group-specific deviation from the common mean, .
Priors
If we view the ANOVA model as a special case of a linear regression
model with only dummy variables as predictors, then the model could be
estimated using the prior specification in the stan_lm
function. In fact, this is exactly how the stan_aov
function is coded. These functions require the user to specify a value
for the prior location (by default the mode) of the
,
the proportion of variance in the outcome attributable to the predictors
under a linear model. This prior specification is appealing in an ANOVA
context because of the fundamental identity
where
stands for sum-of-squares. If we normalize this identity, we obtain the
tautology
but it is reasonable to expect a researcher to have a plausible guess
for
before conducting an ANOVA. See the vignette for
the stan_lm function (regularized linear models) for more
information on this approach.
If we view the ANOVA model as a difference of means, then the model
could be estimated using the prior specification in the
stan_lmer function. In the syntax popularized by the
lme4 package, y ~ 1 + (1|group) represents
a likelihood where
and
is normally distributed across the
groups with mean zero and some unknown standard deviation. The
stan_lmer function specifies that this standard deviation
has a Gamma prior with, by default, both its shape and scale parameters
equal to
,
which is just an standard exponential distribution. However, the shape
and scale parameters can be specified as other positive values. This
approach also requires specifying a prior distribution on the standard
deviation of the errors that is independent of the prior distribution
for each
.
See the vignette for the
stan_glmer function (lme4-style models
using rstanarm) for more information on this
approach.
Example
We will utilize an example from the HSAUR3 package by Brian S. Everitt and Torsten Hothorn, which is used in their 2014 book A Handbook of Statistical Analyses Using R (3rd Edition) (Chapman & Hall / CRC). This book is frequentist in nature and we will show how to obtain the corresponding Bayesian results.
The model in section 4.3.1 analyzes an experiment where rats were subjected to different diets in order to see how much weight they gained. The experimental factors were whether their diet had low or high protein and whether the protein was derived from beef or cereal. Before seeing the data, one might expect that a moderate proportion of the variance in weight gain might be attributed to protein (source) in the diet. The frequentist ANOVA estimates can be obtained:
To obtain Bayesian estimates we can prepend stan_ to
aov and specify the prior location of the
as well as optionally the number of cores that the computer is allowed
to utilize:
library(rstanarm)
post1 <- stan_aov(weightgain ~ source * type, data = weightgain,
prior = R2(location = 0.5), adapt_delta = 0.999,
seed = 12345)
post1Here we have specified adapt_delta = 0.999 to decrease
the stepsize and largely prevent divergent transitions. See the
Troubleshooting section in the main rstanarm vignette for more details about
adapt_delta. Also, our prior guess that
was overly optimistic. However, the frequentist estimates presumably
overfit the data even more.
Alternatively, we could prepend stan_ to
lmer and specify the corresponding priors
post2 <- stan_lmer(weightgain ~ 1 + (1|source) + (1|type) + (1|source:type),
data = weightgain, prior_intercept = cauchy(),
prior_covariance = decov(shape = 2, scale = 2),
adapt_delta = 0.999, seed = 12345)Comparing these two models using the loo function in the
loo package reveals a negligible preference for the
first approach that is almost entirely due to its having a smaller
number of effective parameters as a result of the more regularizing
priors. However, the difference is so small that it may seem
advantageous to present the second results which are more in line with a
mainstream Bayesian approach to an ANOVA model.
Conclusion
This vignette has compared and contrasted two approaches to estimating an ANOVA model with Bayesian techniques using the rstanarm package. They both have the same likelihood, so the (small in this case) differences in the results are attributable to differences in the priors.
The stan_aov approach just calls stan_lm
and thus only requires a prior location on the
of the linear model. This seems rather easy to do in the context of an
ANOVA decomposition of the total sum-of-squares in the outcome into
model sum-of-squares and residual sum-of-squares.
The stan_lmer approach just calls stan_glm
but specifies a normal prior with mean zero for the deviations from
across groups. This is more in line with what most Bayesians would do
naturally — particularly if the factors were considered “random” — but
also requires a prior for
,
,
and the standard deviation of the normal prior on the group-level
intercepts. The stan_lmer approach is very flexible and
might be more appropriate for more complicated experimental designs.