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.
fit1 <- brm(
mvbind(tarsus, back) ~ sex + hatchdate + (1|p|fosternest) + (1|q|dam),
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)
Samples: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
total post-warmup samples = 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 1.00 870
sd(back_Intercept) 0.25 0.07 0.11 0.40 1.00 368
cor(tarsus_Intercept,back_Intercept) -0.51 0.22 -0.92 -0.09 1.00 559
Tail_ESS
sd(tarsus_Intercept) 1468
sd(back_Intercept) 1114
cor(tarsus_Intercept,back_Intercept) 945
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.27 0.05 0.16 0.37 1.00 727
sd(back_Intercept) 0.35 0.06 0.22 0.46 1.00 511
cor(tarsus_Intercept,back_Intercept) 0.69 0.21 0.22 0.98 1.01 305
Tail_ESS
sd(tarsus_Intercept) 950
sd(back_Intercept) 911
cor(tarsus_Intercept,back_Intercept) 774
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 1661 1322
back_Intercept -0.01 0.07 -0.15 0.12 1.00 3151 1484
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 3536 1708
tarsus_sexUNK 0.23 0.13 -0.03 0.48 1.00 3949 1565
tarsus_hatchdate -0.04 0.06 -0.16 0.07 1.00 1562 1455
back_sexMale 0.01 0.07 -0.13 0.14 1.00 5312 1461
back_sexUNK 0.15 0.15 -0.14 0.42 1.00 3480 1621
back_hatchdate -0.09 0.05 -0.19 0.01 1.00 2479 1552
Family Specific Parameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_tarsus 0.76 0.02 0.71 0.80 1.00 2779 1409
sigma_back 0.90 0.02 0.86 0.95 1.00 2881 1361
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 2858 1664
Samples were drawn 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 0.4343598 0.02309208 0.3883864 0.4774232
R2back 0.1992704 0.02780326 0.1444680 0.2532899
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, 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)
Samples: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
total post-warmup samples = 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 1079
sd(back_Intercept) 0.25 0.07 0.09 0.39 1.00 426
cor(tarsus_Intercept,back_Intercept) -0.50 0.22 -0.94 -0.09 1.00 539
Tail_ESS
sd(tarsus_Intercept) 1694
sd(back_Intercept) 541
cor(tarsus_Intercept,back_Intercept) 478
~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 0.37 1.00 827
sd(back_Intercept) 0.35 0.06 0.23 0.46 1.00 587
cor(tarsus_Intercept,back_Intercept) 0.69 0.20 0.23 0.98 1.00 343
Tail_ESS
sd(tarsus_Intercept) 1115
sd(back_Intercept) 1007
cor(tarsus_Intercept,back_Intercept) 632
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 1994 1353
back_Intercept 0.00 0.06 -0.10 0.11 1.00 2720 1594
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 4020 1668
tarsus_sexUNK 0.23 0.13 -0.02 0.48 1.00 3722 1459
back_hatchdate -0.09 0.05 -0.18 0.02 1.00 2744 1669
Family Specific Parameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_tarsus 0.76 0.02 0.71 0.80 1.00 2448 1724
sigma_back 0.90 0.02 0.86 0.95 1.00 2534 1609
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 3001 1519
Samples were drawn 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 -2125.5 33.6
p_loo 175.5 7.2
looic 4250.9 67.1
------
Monte Carlo SE of elpd_loo is NA.
Pareto k diagnostic values:
Count Pct. Min. n_eff
(-Inf, 0.5] (good) 811 97.9% 192
(0.5, 0.7] (ok) 16 1.9% 75
(0.7, 1] (bad) 1 0.1% 41
(1, Inf) (very bad) 0 0.0% <NA>
See help('pareto-k-diagnostic') for details.
Output of model 'fit2':
Computed from 2000 by 828 log-likelihood matrix
Estimate SE
elpd_loo -2125.3 33.6
p_loo 174.2 7.4
looic 4250.5 67.1
------
Monte Carlo SE of elpd_loo is NA.
Pareto k diagnostic values:
Count Pct. Min. n_eff
(-Inf, 0.5] (good) 813 98.2% 220
(0.5, 0.7] (ok) 13 1.6% 166
(0.7, 1] (bad) 2 0.2% 53
(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 -0.2 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)
Samples: 2 chains, each with iter = 2000; warmup = 1000; thin = 1;
total post-warmup samples = 2000
Smooth Terms:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sds(back_shatchdate_1) 2.05 1.10 0.36 4.66 1.00 667 713
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 1.00 805
sd(back_Intercept) 0.23 0.07 0.10 0.37 1.00 401
cor(tarsus_Intercept,back_Intercept) -0.53 0.22 -0.93 -0.07 1.00 456
Tail_ESS
sd(tarsus_Intercept) 1115
sd(back_Intercept) 849
cor(tarsus_Intercept,back_Intercept) 644
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.26 0.06 0.14 0.37 1.00 531
sd(back_Intercept) 0.31 0.06 0.20 0.43 1.00 514
cor(tarsus_Intercept,back_Intercept) 0.65 0.22 0.15 0.98 1.01 258
Tail_ESS
sd(tarsus_Intercept) 566
sd(back_Intercept) 755
cor(tarsus_Intercept,back_Intercept) 571
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 1.01 935 1232
back_Intercept 0.00 0.05 -0.10 0.10 1.00 1545 1390
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 3099 1436
tarsus_sexUNK 0.21 0.12 -0.02 0.44 1.00 2663 1264
sigma_tarsus_sexFem -0.30 0.04 -0.38 -0.22 1.00 1696 1296
sigma_tarsus_sexMale -0.24 0.04 -0.32 -0.17 1.00 2264 1467
sigma_tarsus_sexUNK -0.39 0.12 -0.63 -0.15 1.00 1959 1477
back_shatchdate_1 -0.39 3.30 -5.93 6.89 1.00 968 1113
Family Specific Parameters:
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS Tail_ESS
sigma_back 0.90 0.02 0.85 0.95 1.00 2469 1640
alpha_tarsus -1.22 0.43 -1.87 0.07 1.00 1386 573
Samples were drawn 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.