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).
data("BTdata", package = "MCMCglmm")
head(BTdata)
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)
<- brm(bform1, data = BTdata, chains = 2, cores = 2) fit1
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
<- add_criterion(fit1, "loo")
fit1 summary(fit1)
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 0.59 1.00 773
sd(back_Intercept) 0.25 0.08 0.10 0.39 1.01 253
cor(tarsus_Intercept,back_Intercept) -0.51 0.21 -0.91 -0.07 1.00 468
Tail_ESS
sd(tarsus_Intercept) 1301
sd(back_Intercept) 445
cor(tarsus_Intercept,back_Intercept) 759
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.27 0.06 0.17 0.38 1.00 526
sd(back_Intercept) 0.35 0.06 0.23 0.47 1.00 441
cor(tarsus_Intercept,back_Intercept) 0.69 0.21 0.19 0.99 1.04 136
Tail_ESS
sd(tarsus_Intercept) 862
sd(back_Intercept) 947
cor(tarsus_Intercept,back_Intercept) 517
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 -0.27 1.00 1303 1307
back_Intercept -0.01 0.06 -0.14 0.11 1.00 2243 1668
tarsus_sexMale 0.77 0.06 0.65 0.88 1.00 4070 1440
tarsus_sexUNK 0.23 0.13 -0.03 0.48 1.00 3196 1554
tarsus_hatchdate -0.04 0.06 -0.16 0.07 1.00 1056 1305
back_sexMale 0.01 0.07 -0.12 0.14 1.00 4881 1422
back_sexUNK 0.15 0.14 -0.12 0.42 1.00 3668 1653
back_hatchdate -0.09 0.05 -0.19 0.01 1.00 1789 1304
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 2758 1442
sigma_back 0.90 0.02 0.86 0.95 1.00 3230 1495
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 3343 1663
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.
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 0.4339755 0.02387684 0.3845041 0.4763270
R2back 0.1980269 0.02823697 0.1440005 0.2526271
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 ~ sex + (1|p|fosternest) + (1|q|dam))
bf_tarsus <- bf(back ~ hatchdate + (1|p|fosternest) + (1|q|dam))
bf_back <- brm(bf_tarsus + bf_back + set_rescor(TRUE),
fit2 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.
<- add_criterion(fit2, "loo")
fit2 summary(fit2)
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 0.59 1.00 944
sd(back_Intercept) 0.25 0.07 0.10 0.39 1.00 416
cor(tarsus_Intercept,back_Intercept) -0.50 0.22 -0.90 -0.07 1.00 791
Tail_ESS
sd(tarsus_Intercept) 1404
sd(back_Intercept) 572
cor(tarsus_Intercept,back_Intercept) 1072
~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 0.38 1.00 678
sd(back_Intercept) 0.35 0.06 0.23 0.47 1.00 558
cor(tarsus_Intercept,back_Intercept) 0.68 0.21 0.20 0.98 1.00 291
Tail_ESS
sd(tarsus_Intercept) 1227
sd(back_Intercept) 874
cor(tarsus_Intercept,back_Intercept) 681
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 2059 1785
back_Intercept 0.00 0.05 -0.11 0.11 1.00 2807 1746
tarsus_sexMale 0.77 0.06 0.66 0.88 1.00 4227 1517
tarsus_sexUNK 0.23 0.13 -0.02 0.48 1.00 4517 1520
back_hatchdate -0.08 0.05 -0.19 0.02 1.00 3182 1470
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 0.79 1.00 2038 1659
sigma_back 0.90 0.02 0.86 0.95 1.00 2406 1053
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 3349 1630
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 -2126.0 33.6
p_loo 175.6 7.4
looic 4252.0 67.3
------
Monte Carlo SE of elpd_loo is NA.
Pareto k diagnostic values:
Count Pct. Min. n_eff
(-Inf, 0.5] (good) 803 97.0% 394
(0.5, 0.7] (ok) 23 2.8% 105
(0.7, 1] (bad) 2 0.2% 26
(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 -2123.2 33.7
p_loo 173.8 7.5
looic 4246.5 67.4
------
Monte Carlo SE of elpd_loo is NA.
Pareto k diagnostic values:
Count Pct. Min. n_eff
(-Inf, 0.5] (good) 809 97.7% 370
(0.5, 0.7] (ok) 17 2.1% 95
(0.7, 1] (bad) 2 0.2% 28
(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 -2.8 1.4
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 ~ sex + (1|p|fosternest) + (1|q|dam)) +
bf_tarsus lf(sigma ~ 0 + sex) + skew_normal()
<- bf(back ~ s(hatchdate) + (1|p|fosternest) + (1|q|dam)) +
bf_back gaussian()
<- brm(
fit3 + bf_back + set_rescor(FALSE),
bf_tarsus data = BTdata, chains = 2, cores = 2,
control = list(adapt_delta = 0.95)
)
Again, we summarize the model and look at some posterior-predictive checks.
<- add_criterion(fit3, "loo")
fit3 summary(fit3)
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) 1.97 0.99 0.25 4.22 1.00 503 338
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 1.00 832
sd(back_Intercept) 0.24 0.07 0.10 0.37 1.01 298
cor(tarsus_Intercept,back_Intercept) -0.52 0.22 -0.93 -0.06 1.00 417
Tail_ESS
sd(tarsus_Intercept) 1395
sd(back_Intercept) 681
cor(tarsus_Intercept,back_Intercept) 445
~fosternest (Number of levels: 104)
Estimate Est.Error l-95% CI u-95% CI Rhat Bulk_ESS
sd(tarsus_Intercept) 0.26 0.05 0.15 0.37 1.00 535
sd(back_Intercept) 0.31 0.06 0.20 0.42 1.00 512
cor(tarsus_Intercept,back_Intercept) 0.65 0.22 0.13 0.98 1.00 255
Tail_ESS
sd(tarsus_Intercept) 856
sd(back_Intercept) 1060
cor(tarsus_Intercept,back_Intercept) 530
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 1.00 977 1420
back_Intercept 0.00 0.05 -0.10 0.11 1.00 1475 1602
tarsus_sexMale 0.77 0.06 0.65 0.88 1.00 3099 1461
tarsus_sexUNK 0.21 0.12 -0.02 0.45 1.00 2394 1305
sigma_tarsus_sexFem -0.30 0.04 -0.38 -0.22 1.00 2537 1613
sigma_tarsus_sexMale -0.25 0.04 -0.33 -0.17 1.00 2200 1266
sigma_tarsus_sexUNK -0.39 0.13 -0.64 -0.12 1.00 1839 1461
back_shatchdate_1 -0.35 3.16 -6.14 6.59 1.00 1044 1029
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 2296 1301
alpha_tarsus -1.22 0.43 -1.89 0.07 1.00 1626 682
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.
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.