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
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
Family: MV(gaussian, gaussian)
Links: mu = identity; sigma = identity
mu = identity; sigma = 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
Group-Level Effects:
~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 1.00 775
sd(back_Intercept) 0.25 0.07 0.10 0.40 1.01 319
cor(tarsus_Intercept,back_Intercept) -0.51 0.23 -0.93 -0.05 1.00 545
Tail_ESS
sd(tarsus_Intercept) 1084
sd(back_Intercept) 821
cor(tarsus_Intercept,back_Intercept) 705
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.27 0.05 0.17 0.38 1.00 728
sd(back_Intercept) 0.35 0.06 0.23 0.47 1.00 570
cor(tarsus_Intercept,back_Intercept) 0.69 0.21 0.21 0.98 1.00 278
Tail_ESS
sd(tarsus_Intercept) 1170
sd(back_Intercept) 727
cor(tarsus_Intercept,back_Intercept) 543
Population-Level Effects:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
tarsus_Intercept -0.41 0.07 -0.54 -0.27 1.00 1500 1673
back_Intercept -0.01 0.06 -0.13 0.11 1.00 2712 1635
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 3208 1216
tarsus_sexUNK 0.23 0.12 -0.01 0.48 1.00 3197 1555
tarsus_hatchdate -0.04 0.06 -0.16 0.07 1.00 1700 1559
back_sexMale 0.01 0.07 -0.11 0.14 1.00 3550 1449
back_sexUNK 0.15 0.15 -0.14 0.44 1.00 3725 1785
back_hatchdate -0.09 0.05 -0.19 0.01 1.00 2279 1711
Family Specific 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 2145 1426
sigma_back 0.90 0.02 0.85 0.95 1.00 1792 1338
Residual Correlations:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
rescor(tarsus,back) -0.05 0.04 -0.13 0.02 1.00 1941 1462
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. Within dams, tarsus length and back color
seem to be negatively correlated, while within 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.
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.
Estimate Est.Error Q2.5 Q97.5
R2tarsus 0.4340621 0.02266112 0.3884670 0.4761039
R2back 0.1992222 0.02871862 0.1435727 0.2535659
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.
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.
Family: MV(gaussian, gaussian)
Links: mu = identity; sigma = identity
mu = identity; sigma = 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
Group-Level Effects:
~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 1.00 735
sd(back_Intercept) 0.24 0.07 0.10 0.39 1.00 374
cor(tarsus_Intercept,back_Intercept) -0.51 0.22 -0.93 -0.03 1.00 537
Tail_ESS
sd(tarsus_Intercept) 1172
sd(back_Intercept) 396
cor(tarsus_Intercept,back_Intercept) 610
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.26 0.05 0.16 0.37 1.00 826
sd(back_Intercept) 0.35 0.06 0.23 0.46 1.00 662
cor(tarsus_Intercept,back_Intercept) 0.66 0.22 0.16 0.98 1.00 227
Tail_ESS
sd(tarsus_Intercept) 1308
sd(back_Intercept) 998
cor(tarsus_Intercept,back_Intercept) 584
Population-Level Effects:
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 1735 1493
back_Intercept -0.00 0.05 -0.11 0.10 1.00 2547 1636
tarsus_sexMale 0.77 0.06 0.66 0.88 1.01 3794 1492
tarsus_sexUNK 0.23 0.13 -0.02 0.48 1.00 3534 1696
back_hatchdate -0.09 0.05 -0.19 0.02 1.00 2217 1694
Family Specific 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 2152 1598
sigma_back 0.90 0.02 0.85 0.95 1.00 2817 1490
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 3603 1634
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:
Output of model 'fit1':
Computed from 2000 by 828 log-likelihood matrix
Estimate SE
elpd_loo -2127.1 33.6
p_loo 177.0 7.3
looic 4254.1 67.2
------
Monte Carlo SE of elpd_loo is 0.4.
Pareto k diagnostic values:
Count Pct. Min. n_eff
(-Inf, 0.5] (good) 808 97.6% 149
(0.5, 0.7] (ok) 20 2.4% 76
(0.7, 1] (bad) 0 0.0% <NA>
(1, Inf) (very bad) 0 0.0% <NA>
All Pareto k estimates are ok (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 -2124.6 33.7
p_loo 173.4 7.3
looic 4249.1 67.3
------
Monte Carlo SE of elpd_loo is NA.
Pareto k diagnostic values:
Count Pct. Min. n_eff
(-Inf, 0.5] (good) 813 98.2% 268
(0.5, 0.7] (ok) 13 1.6% 172
(0.7, 1] (bad) 2 0.2% 52
(1, Inf) (very bad) 0 0.0% <NA>
See help('pareto-k-diagnostic') for details.
Model comparisons:
elpd_diff se_diff
fit2 0.0 0.0
fit1 -2.5 1.3
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.
Family: MV(skew_normal, gaussian)
Links: mu = identity; sigma = log; alpha = identity
mu = identity; sigma = 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
Smooth Terms:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sds(back_shatchdate_1) 1.98 1.05 0.30 4.41 1.00 463 390
Group-Level Effects:
~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 0.58 1.00 757
sd(back_Intercept) 0.24 0.07 0.08 0.38 1.00 275
cor(tarsus_Intercept,back_Intercept) -0.50 0.23 -0.92 -0.03 1.01 528
Tail_ESS
sd(tarsus_Intercept) 1208
sd(back_Intercept) 333
cor(tarsus_Intercept,back_Intercept) 636
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.26 0.06 0.15 0.37 1.00 554
sd(back_Intercept) 0.31 0.06 0.19 0.43 1.00 548
cor(tarsus_Intercept,back_Intercept) 0.63 0.24 0.09 0.97 1.00 282
Tail_ESS
sd(tarsus_Intercept) 878
sd(back_Intercept) 762
cor(tarsus_Intercept,back_Intercept) 581
Population-Level Effects:
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 1238 1559
back_Intercept 0.00 0.05 -0.10 0.11 1.00 1568 1142
tarsus_sexMale 0.77 0.06 0.66 0.89 1.00 3076 1610
tarsus_sexUNK 0.21 0.12 -0.02 0.44 1.00 3235 1607
sigma_tarsus_sexFem -0.30 0.04 -0.38 -0.21 1.00 2876 1553
sigma_tarsus_sexMale -0.24 0.04 -0.32 -0.16 1.00 2353 1724
sigma_tarsus_sexUNK -0.39 0.12 -0.63 -0.15 1.00 2236 1378
back_shatchdate_1 -0.23 3.24 -5.82 7.39 1.00 1016 1027
Family Specific Parameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_back 0.90 0.03 0.85 0.95 1.00 1992 1579
alpha_tarsus -1.24 0.41 -1.91 -0.11 1.00 1549 750
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
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.
Hadfield JD, Nutall A, Osorio D, Owens IPF (2007). Testing the phenotypic gambit: phenotypic, genetic and environmental correlations of colour. Journal of Evolutionary Biology, 20(2), 549-557.