Estimating Multivariate Models with brms
Paul Bürkner
2026-09-25
Source:vignettes/brms_multivariate.Rmd
brms_multivariate.RmdIntroduction
In the present vignette, we want to discuss how to specify
multivariate multilevel models using brms. We call a
model multivariate if it contains multiple response variables,
each being predicted by its own set of predictors. Consider an example
from biology. Hadfield, Nutall, Osorio, and Owens (2007) analyzed data
of the Eurasian blue tit (https://en.wikipedia.org/wiki/Eurasian_blue_tit). They
predicted the tarsus length as well as the
back color of chicks. Half of the brood were put into
another fosternest, while the other half stayed in the
fosternest of their own dam. This allows to separate
genetic from environmental factors. Additionally, we have information
about the hatchdate and sex of the chicks (the
latter being known for 94% of the animals).
tarsus back animal dam fosternest hatchdate sex
1 -1.89229718 1.1464212 R187142 R187557 F2102 -0.6874021 Fem
2 1.13610981 -0.7596521 R187154 R187559 F1902 -0.6874021 Male
3 0.98468946 0.1449373 R187341 R187568 A602 -0.4279814 Male
4 0.37900806 0.2555847 R046169 R187518 A1302 -1.4656641 Male
5 -0.07525299 -0.3006992 R046161 R187528 A2602 -1.4656641 Fem
6 -1.13519543 1.5577219 R187409 R187945 C2302 0.3502805 Fem
Basic Multivariate Models
We begin with a relatively simple multivariate normal model.
bform1 <-
bf(mvbind(tarsus, back) ~ sex + hatchdate + (1|p|fosternest) + (1|q|dam)) +
set_rescor(TRUE)
fit1 <- brm(bform1, data = BTdata, chains = 2, cores = 2)As can be seen in the model code, we have used mvbind
notation to tell brms that both tarsus and
back are separate response variables. The term
(1|p|fosternest) indicates a varying intercept over
fosternest. By writing |p| in between we
indicate that all varying effects of fosternest should be
modeled as correlated. This makes sense since we actually have two model
parts, one for tarsus and one for back. The
indicator p is arbitrary and can be replaced by other
symbols that comes into your mind (for details about the multilevel
syntax of brms, see help("brmsformula")
and vignette("brms_multilevel")). Similarly, the term
(1|q|dam) indicates correlated varying effects of the
genetic mother of the chicks. Alternatively, we could have also modeled
the genetic similarities through pedigrees and corresponding relatedness
matrices, but this is not the focus of this vignette (please see
vignette("brms_phylogenetics")). The model results are
readily summarized via
fit1 <- add_criterion(fit1, "loo")
summary(fit1) Family: MV(gaussian, gaussian)
Links: mu = identity
mu = identity
Formula: tarsus ~ sex + hatchdate + (1 | p | fosternest) + (1 | q | dam)
back ~ sex + hatchdate + (1 | p | fosternest) + (1 | q | dam)
Data: BTdata (Number of observations: 828)
Draws: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
total post-warmup draws = 2000
Multilevel Hyperparameters:
~dam (Number of levels: 106)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.49 0.05 0.39 0.59 1.00 667
sd(back_Intercept) 0.25 0.07 0.10 0.40 1.00 261
cor(tarsus_Intercept,back_Intercept) -0.52 0.22 -0.93 -0.07 1.00 426
Tail_ESS
sd(tarsus_Intercept) 860
sd(back_Intercept) 499
cor(tarsus_Intercept,back_Intercept) 623
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.27 0.06 0.16 0.38 1.00 589
sd(back_Intercept) 0.35 0.06 0.23 0.47 1.00 416
cor(tarsus_Intercept,back_Intercept) 0.71 0.21 0.23 0.99 1.00 224
Tail_ESS
sd(tarsus_Intercept) 1019
sd(back_Intercept) 847
cor(tarsus_Intercept,back_Intercept) 332
Regression Coefficients:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
tarsus_Intercept -0.41 0.07 -0.54 -0.28 1.00 659 855
back_Intercept -0.01 0.06 -0.14 0.12 1.00 1285 1336
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 2512 1387
tarsus_sexUNK 0.23 0.13 -0.02 0.48 1.00 2273 1533
tarsus_hatchdate -0.04 0.06 -0.16 0.07 1.00 669 1086
back_sexMale 0.01 0.07 -0.12 0.14 1.00 2355 1415
back_sexUNK 0.15 0.15 -0.16 0.44 1.00 2504 1785
back_hatchdate -0.09 0.05 -0.19 0.02 1.00 1197 1235
Further Distributional Parameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_tarsus 0.76 0.02 0.72 0.80 1.00 2013 1525
sigma_back 0.90 0.02 0.85 0.95 1.00 1872 1417
Residual Correlations:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
rescor(tarsus,back) -0.05 0.04 -0.12 0.02 1.00 1981 1515
Draws were sampled using sampling(NUTS). For each parameter, Bulk_ESS
and Tail_ESS are effective sample size measures, and Rhat is the potential
scale reduction factor on split chains (at convergence, Rhat = 1).
The summary output of multivariate models closely resembles those of
univariate models, except that the parameters now have the corresponding
response variable as prefix. Across dams, tarsus length and back color
seem to be negatively correlated, while across fosternests the opposite
is true. This indicates differential effects of genetic and
environmental factors on these two characteristics. Further, the small
residual correlation rescor(tarsus, back) on the bottom of
the output indicates that there is little unmodeled dependency between
tarsus length and back color. Although not necessary at this point, we
have already computed and stored the LOO information criterion of
fit1, which we will use for model comparisons. Next, let’s
take a look at some posterior-predictive checks, which give us a first
impression of the model fit.
pp_check(fit1, resp = "tarsus")
pp_check(fit1, resp = "back")
This looks pretty solid, but we notice a slight unmodeled left
skewness in the distribution of tarsus. We will come back
to this later on. Next, we want to investigate how much variation in the
response variables can be explained by our model and we use a Bayesian
generalization of the \(R^2\)
coefficient.
bayes_R2(fit1) Estimate Est.Error Q2.5 Q97.5
R2tarsus 0.4340254 0.0264582 0.3797048 0.4826320
R2back 0.1985098 0.0286021 0.1440022 0.2539625
Clearly, there is much variation in both animal characteristics that we can not explain, but apparently we can explain more of the variation in tarsus length than in back color.
More Complex Multivariate Models
Now, suppose we only want to control for sex in
tarsus but not in back and vice versa for
hatchdate. Not that this is particular reasonable for the
present example, but it allows us to illustrate how to specify different
formulas for different response variables. We can no longer use
mvbind syntax and so we have to use a more verbose
approach:
bf_tarsus <- bf(tarsus ~ sex + (1|p|fosternest) + (1|q|dam))
bf_back <- bf(back ~ hatchdate + (1|p|fosternest) + (1|q|dam))
fit2 <- brm(bf_tarsus + bf_back + set_rescor(TRUE),
data = BTdata, chains = 2, cores = 2)Note that we have literally added the two model parts via
the + operator, which is in this case equivalent to writing
mvbf(bf_tarsus, bf_back). See
help("brmsformula") and help("mvbrmsformula")
for more details about this syntax. Again, we summarize the model
first.
fit2 <- add_criterion(fit2, "loo")
summary(fit2) Family: MV(gaussian, gaussian)
Links: mu = identity
mu = identity
Formula: tarsus ~ sex + (1 | p | fosternest) + (1 | q | dam)
back ~ hatchdate + (1 | p | fosternest) + (1 | q | dam)
Data: BTdata (Number of observations: 828)
Draws: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
total post-warmup draws = 2000
Multilevel Hyperparameters:
~dam (Number of levels: 106)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.48 0.05 0.39 0.58 1.00 619
sd(back_Intercept) 0.25 0.07 0.11 0.40 1.00 296
cor(tarsus_Intercept,back_Intercept) -0.50 0.22 -0.93 -0.06 1.01 310
Tail_ESS
sd(tarsus_Intercept) 1275
sd(back_Intercept) 578
cor(tarsus_Intercept,back_Intercept) 548
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.27 0.06 0.16 0.38 1.00 466
sd(back_Intercept) 0.35 0.06 0.23 0.47 1.00 533
cor(tarsus_Intercept,back_Intercept) 0.70 0.19 0.26 0.98 1.00 254
Tail_ESS
sd(tarsus_Intercept) 800
sd(back_Intercept) 805
cor(tarsus_Intercept,back_Intercept) 349
Regression Coefficients:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
tarsus_Intercept -0.41 0.07 -0.55 -0.28 1.01 824 855
back_Intercept 0.00 0.05 -0.11 0.10 1.00 1320 1339
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 2459 1397
tarsus_sexUNK 0.22 0.13 -0.04 0.48 1.00 2948 1425
back_hatchdate -0.08 0.05 -0.19 0.02 1.00 1255 1687
Further Distributional Parameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_tarsus 0.76 0.02 0.72 0.80 1.00 1571 1120
sigma_back 0.90 0.02 0.85 0.95 1.00 1718 1480
Residual Correlations:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
rescor(tarsus,back) -0.05 0.04 -0.12 0.02 1.00 2187 1296
Draws were sampled using sampling(NUTS). For each parameter, Bulk_ESS
and Tail_ESS are effective sample size measures, and Rhat is the potential
scale reduction factor on split chains (at convergence, Rhat = 1).
Let’s find out, how model fit changed due to excluding certain effects from the initial model:
loo(fit1, fit2)Output of model 'fit1':
Computed from 2000 by 828 log-likelihood matrix.
Estimate SE
elpd_loo -2124.4 33.6
p_loo 174.5 7.3
looic 4248.9 67.1
------
MCSE of elpd_loo is 0.4.
MCSE and ESS estimates assume MCMC draws (r_eff in [0.3, 1.8]).
All Pareto k estimates are good (k < 0.7).
See help('pareto-k-diagnostic') for details.
Output of model 'fit2':
Computed from 2000 by 828 log-likelihood matrix.
Estimate SE
elpd_loo -2123.7 33.6
p_loo 173.5 7.3
looic 4247.3 67.2
------
MCSE of elpd_loo is NA.
MCSE and ESS estimates assume MCMC draws (r_eff in [0.4, 1.6]).
Pareto k diagnostic values:
Count Pct. Min. ESS
(-Inf, 0.7] (good) 827 99.9% 96
(0.7, 1] (bad) 1 0.1% <NA>
(1, Inf) (very bad) 0 0.0% <NA>
See help('pareto-k-diagnostic') for details.
Model comparisons:
model elpd_diff se_diff p_worse diag_diff diag_elpd
fit2 0.0 0.0 NA 1 k_psis > 0.7
fit1 -0.8 1.3 0.72 |elpd_diff| < 4
Apparently, there is no noteworthy difference in the model fit.
Accordingly, we do not really need to model sex and
hatchdate for both response variables, but there is also no
harm in including them (so I would probably just include them).
To give you a glimpse of the capabilities of brms’
multivariate syntax, we change our model in various directions at the
same time. Remember the slight left skewness of tarsus,
which we will now model by using the skew_normal family
instead of the gaussian family. Since we do not have a
multivariate normal (or student-t) model, anymore, estimating residual
correlations is no longer possible. We make this explicit using the
set_rescor function. Further, we investigate if the
relationship of back and hatchdate is really
linear as previously assumed by fitting a non-linear spline of
hatchdate. On top of it, we model separate residual
variances of tarsus for male and female chicks.
bf_tarsus <- bf(tarsus ~ sex + (1|p|fosternest) + (1|q|dam)) +
lf(sigma ~ 0 + sex) + skew_normal()
bf_back <- bf(back ~ s(hatchdate) + (1|p|fosternest) + (1|q|dam)) +
gaussian()
fit3 <- brm(
bf_tarsus + bf_back + set_rescor(FALSE),
data = BTdata, chains = 2, cores = 2,
control = list(adapt_delta = 0.95)
)Again, we summarize the model and look at some posterior-predictive checks.
fit3 <- add_criterion(fit3, "loo")
summary(fit3) Family: MV(skew_normal, gaussian)
Links: mu = identity; sigma = log
mu = identity
Formula: tarsus ~ sex + (1 | p | fosternest) + (1 | q | dam)
sigma ~ 0 + sex
back ~ s(hatchdate) + (1 | p | fosternest) + (1 | q | dam)
Data: BTdata (Number of observations: 828)
Draws: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
total post-warmup draws = 2000
Smoothing Spline Hyperparameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sds(back_shatchdate_1) 2.05 1.08 0.35 4.61 1.00 439 390
Multilevel Hyperparameters:
~dam (Number of levels: 106)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.47 0.05 0.38 0.57 1.01 496
sd(back_Intercept) 0.23 0.07 0.10 0.36 1.01 250
cor(tarsus_Intercept,back_Intercept) -0.53 0.23 -0.95 -0.06 1.01 362
Tail_ESS
sd(tarsus_Intercept) 716
sd(back_Intercept) 419
cor(tarsus_Intercept,back_Intercept) 464
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.27 0.06 0.15 0.38 1.00 401
sd(back_Intercept) 0.31 0.06 0.20 0.42 1.00 357
cor(tarsus_Intercept,back_Intercept) 0.65 0.21 0.18 0.97 1.02 210
Tail_ESS
sd(tarsus_Intercept) 700
sd(back_Intercept) 662
cor(tarsus_Intercept,back_Intercept) 486
Regression Coefficients:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
tarsus_Intercept -0.41 0.07 -0.55 -0.28 1.00 794 1109
back_Intercept 0.00 0.05 -0.10 0.10 1.00 1120 1482
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 2457 1507
tarsus_sexUNK 0.22 0.12 -0.00 0.45 1.00 2078 1422
sigma_tarsus_sexFem -0.30 0.04 -0.38 -0.22 1.00 2417 1555
sigma_tarsus_sexMale -0.25 0.04 -0.32 -0.16 1.00 2146 1753
sigma_tarsus_sexUNK -0.40 0.13 -0.66 -0.15 1.00 2056 1415
back_shatchdate_1 -0.07 3.19 -5.79 7.17 1.00 823 1172
Further Distributional Parameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_back 0.90 0.02 0.86 0.95 1.00 1379 1297
alpha_tarsus -1.25 0.42 -1.91 -0.14 1.00 1304 553
Draws were sampled using sampling(NUTS). For each parameter, Bulk_ESS
and Tail_ESS are effective sample size measures, and Rhat is the potential
scale reduction factor on split chains (at convergence, Rhat = 1).
We see that the (log) residual standard deviation of
tarsus is somewhat larger for chicks whose sex could not be
identified as compared to male or female chicks. Further, we see from
the negative alpha (skewness) parameter of
tarsus that the residuals are indeed slightly left-skewed.
Lastly, running
conditional_effects(fit3, "hatchdate", resp = "back")
reveals a non-linear relationship of hatchdate on the
back color, which seems to change in waves over the course
of the hatch dates.
There are many more modeling options for multivariate models, which
are not discussed in this vignette. Examples include autocorrelation
structures, Gaussian processes, or explicit non-linear predictors (e.g.,
see help("brmsformula") or
vignette("brms_multilevel")). In fact, nearly all the
flexibility of univariate models is retained in multivariate models.