Abstract
Count data can be analyzed using generalized linear mixed models when observations are correlated in ways that require random effects. However, count data are often zero-inflated, containing more zeros than would be expected from the typical error distributions. We present a new package, glmmTMB, and compare it to other R packages that fit zero-inflated mixed models. The glmmTMB package fits many types of GLMMs and extensions, including models with continuously distributed responses, but here we focus on count responses. glmmTMB is faster than glmmADMB, MCMCglmm, and brms, and more flexible than INLA and mgcv for zero-inflated modeling. One unique feature of glmmTMB (among packages that fit zero-inflated mixed models) is its ability to estimate the Conway-Maxwell-Poisson distribution parameterized by the mean. Overall, its most appealing features for new users may be the combination of speed, flexibility, and its interface’s similarity to lme4.Observed response variables are often in the form of discrete count data, e.g., the number of times that owl nestlings beg for food (Roulin and Bersier 2007), counts of salamanders in streams (Price et al. 2016), or counts of parasite eggs in fecal samples of sheep (Denwood et al. 2008). These counts are often analyzed using generalized linear models (GLMs) and their extensions (O’Hara and Kotze 2010; Wilson and Grenfell 1997). GLMs quantify how expected counts change as a function of predictor variables, e.g., nestlings change their behavior depending on which parent they interact with (Roulin and Bersier 2007), salamander abundance decreases in streams affected by coal mining (Price et al. 2016), and helminth infection intensity in sheep decreases in response to treatment with anthelmintic drugs (Wang et al. 2017). Repeated measurements on the same individual, at the same location, or observations during the same time period are often correlated; this correlation can be accounted for using random effects in generalized linear mixed models (GLMMs; (Benjamin M. Bolker et al. 2009; Benjamin M. Bolker 2015)).
These types of count data are commonly modeled with GLMs and GLMMs using either Poisson or negative binomial distributions. For the Poisson distribution, the variance is equal to the mean. When data are overdispersed — meaning the variance is larger than the mean — they are often instead modeled using the negative binomial distribution, which can be defined as a mixture of Poisson distributions with Gamma-distributed rates. Overdispersion can also be addressed by adding a random effect with one level for each observation, i.e., a log-normal Poisson distribution (Elston et al. 2001; Hadfield 2010; Harrison 2014, 2015). Ignoring overdispersion causes confidence intervals to be too narrow and inflates the rate of false positives in statistical tests (Rhodes 2015). When data are either over- or underdispersed, they can be modeled with the lesser-known, Conway-Maxwell-Poisson distribution (Shmueli et al. 2005; Lynch, Thorson, and Shelton 2014; Barriga and Louzada 2014). Depending on the dispersion, the upper tail of the Conway-Maxwell-Poisson distribution can be either longer or shorter than that of the Poisson (K. F. Sellers and Shmueli 2010). With two parameters, the Conway-Maxwell-Poisson is a generalization of the Poisson distribution and, depending on the dispersion parameter, it also includes the Bernoulli and geometric distributions as special cases (K. F. Sellers and Shmueli 2010). Among other generalizations, the Sichel and Delaporte distributions (Stasinopoulos et al. 2017) provide flexibility in skewness in addition to dispersion.
For these distributions, the expected number of zeros decreases as the mean increases. However, when multiple processes underlie the observed counts, the counts can contain many zeros even if the mean is much greater than zero. For example, an observation of a stream with zero salamanders could be a “structural” zero due to the stream being uninhabitable due to mining waste, or a “sampling” zero due to the combination of a low mean (due to poor ecological suitability and/or low detectability) and sampling variation (Price et al. 2016). Zero-inflated (more broadly zero-altered) GLMs allow us to model count data using a mixture of a Poisson, negative binomial, or Conway-Maxwell-Poisson distribution and a structural zero component. Models that ignore zero-inflation, or attempt to handle it in the same way as simple overdispersion, can yield biased parameter estimates (Harrison 2014).
In this article, we outline the R packages available for fitting models to count data while introducing glmmTMB. We assume that the reader already has a basic understanding of GLMs (Buckley 2015), GLMMs (Benjamin M. Bolker 2015), and zero-altered models (Zeileis, Kleiber, and Jackman 2008; Harrison 2014)).
Several R packages are available for fitting zero-inflated models: pscl, INLA, MCMCglmm, glmmADMB, mgcv, brms, and gamlss (Table 1; (Zeileis, Kleiber, and Jackman 2008; HRue, Martino, and Chopin 2009; Hadfield 2010; Skaug et al. 2012; Wood, Pya, and Säfken 2016; Bürkner 2017; Stasinopoulos et al. 2017)). The widely-used pscl package can fit zero-inflated and hurdle GLMs with predictor variables on the zero-inflation using maximum likelihood estimation (MLE: (Zeileis, Kleiber, and Jackman 2008)). For example, pscl can be used to test the hypothesis that sheep fecal egg counts depend on age and structural zeros depend on genotype. However, pscl cannot model the correlation within sampling units caused by repeated samples; this requires random effects. Omitting random effects and thereby ignoring correlation makes statistical inference anti-conservative (Benjamin M. Bolker et al. 2009; Benjamin M. Bolker 2015). Several other packages have similar capabilities for fitting zero-inflated GLMs (flexmix, MXM, VGAM: (Grün and Leisch 2008; Lagani et al. 2017; Yee 2017)), but in this paper we focus on packages that can also estimate random effects. One such package is glmmADMB which can fit zero-inflated GLMMs (Skaug et al. 2012). However, glmmADMB cannot fit models where the degree of zero-inflation varies across observational units; thus, it is only appropriate for models where all observational units have an equal probability of producing a structural zero. INLA has the same limitation as glmmADMB (HRue, Martino, and Chopin 2009). The mgcv package can only fit zero-inflated GLMMs with predictors of zero-inflation when using a Poisson distribution (Wood, Pya, and Säfken 2016). The MCMCglmm and brms packages can fit zero-inflated GLMMs with predictors of zero-inflation, but they are relatively slow (as we will show) because they rely on Markov chain Monte Carlo (MCMC) sampling (Bürkner 2017; Hadfield 2010). gamlss is a flexible package that fits generalized additive models with predictors on all parameters of a distribution; its scope includes several zero-inflated and zero-altered distributions (Stasinopoulos et al. 2017).
The list of features documented here is not exhaustive. It should be appreciated that brms, gamlss and MCMCglmm have additional features that go beyond the scope of zero-inflated GLMMs (Bürkner 2017; Stasinopoulos et al. 2017; Hadfield 2010). We focus on the process of fitting models, largely neglecting questions of statistical frameworks (frequentist vs. Bayesian) or post-fitting procedures such as inference and prediction. For example, having MCMC samples from a fitted model allows a wide range of inferential and predictive procedures.
Here we introduce a new R package, glmmTMB, that estimates GLMs, GLMMs and extensions of GLMMs including zero-inflated and hurdle GLMMs using ML. The ability to fit these types of models quickly and using a single package will make it easier to perform model selection. We focus on zero-inflated counts, but note that there are many other distributions available in glmmTMB, including continuous distributions. We demonstrate the package using two examples without going into details of the reasons why a user would want to fit these models. We use an example of salamander abundance to show how to fit and compare zero-inflated and hurdle GLMMs and then how to extract results from a model. We then use variations of the salamander data to compare how the timings of different packages scale with the number of observations and random effect levels. We use a classic example of owl nestling behavior to compare the timing and parameter estimates from glmmTMB with other R packages.
| Feature | glmmTMB | glmmADMB | MCMCglmm | brms | INLA | mgcv | gamlss | |
|---|---|---|---|---|---|---|---|---|
| hurdle models\(^1\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | |||
| predictors of zero-inflation | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | ||||
| predictors of dispersion | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | |||||
| zero-truncated distributions | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | ||
nbinom2 distribution |
\(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\)\(^2\) | \(\checkmark\) | ||
nbinom1 distribution |
\(\checkmark\) | \(\checkmark\) | \(\checkmark\)\(^2\) | |||||
compois distribution |
\(\checkmark\)\(^3\) | |||||||
| Delaporte distribution | \(\checkmark\)\(^2\) | |||||||
| Sichel distribution | \(\checkmark\) | |||||||
| geometric distribution | \(\checkmark\) | \(\checkmark\) | \(\checkmark\)\(^2\) | |||||
| PIG distribution | \(\checkmark\) | |||||||
| weights | \(\checkmark\)\(^4\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | ||
| offsets | \(\checkmark\) | \(\checkmark\) | \(^5\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | ||
| various RE structures | \(\checkmark\)\(^6\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | |||
| RE cor across components \(^7\) | \(\checkmark\) | \(\checkmark\) | ||||||
| MLE | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | ||||
| MCMC samples\(^8\) | \(\checkmark\)\(^9\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) \(^{10}\) | \(\checkmark\) | ||
| multivariate responses \(^{11}\) | \(\checkmark\) | \(\checkmark\) | ||||||
| GAM \(^{12}\) | \(\checkmark\) | \(\checkmark\) | \(\checkmark\) |
The design goal of glmmTMB is to extend the flexibility of GLMMs in R while maintaining a familiar interface. To maximize flexibility and speed, glmmTMB’s estimation is done using the TMB package (Kristensen et al. 2016), but users need not be familiar with TMB. We based glmmTMB’s interface (e.g., formula syntax) on the lme4 package — one of the most widely used R packages for fitting GLMMs (Bates et al. 2015). Like lme4, glmmTMB uses MLE and the Laplace approximation to integrate over random effects; unlike lme4, glmmTMB does not have the alternative options of doing restricted maximum likelihood (REML) estimation nor using Gauss-Hermite quadrature to integrate over random effects (Benjamin M. Bolker et al. 2009; Benjamin M. Bolker 2015). The Laplace approximation may perform poorly when there is little information available on each random effect level (Ogden 2015). REML may be added to glmmTMB in the future. The underlying implementation using TMB is a fundamental difference compared to lme4 and provides glmmTMB with a speed advantage when estimating non-Gaussian models (Figures 1 and 2) and gives it greater flexibility in the classes of distributions it can fit (Table 1).
The flexibility of glmmTMB enables users to fit and compare many varieties of models with assurance that the log-likelihood values are calculated in a consistent way. Comparing likelihoods of models fit by multiple packages must be done carefully because some packages drop constants from the log-likelihood calculations while others do not.
A glmmTMB model has four main components: a conditional
model formula, a distribution for the conditional model, a dispersion
model formula, and a zero-inflation model formula. Simple GLMs and GLMMs
can be fit using the conditional model while leaving the zero-inflation
and dispersion formulas at their default values. The mean of the
conditional model is specified using a two-sided formula with the
response variable on the left and predictors on the right, potentially
including random effects and offsets. This formula uses the same syntax
as lme4. For example, if salamander counts vary by species
(spp) and vary randomly by site, then the formula for the
dependence of mean count on species could be
count ~ spp + (1 | site)
The distribution around the mean of the conditional model is
specified using the argument family. For the types of count
data described in the introduction, the distribution will typically be
either Poisson or negative binomial. The Conway-Maxwell-Poisson is a
less commonly known distribution for count data that is flexible enough
to fit both over- and underdispersed data. Following the standard of
glmmTMB described above, the Conway-Maxwell-Poisson
distribution (family = compois) is parameterized with the
mean (Huang 2017), which differs from the
COMPoissonReg package(K. Sellers, Lotze, and Raim 2017). The Poisson,
Conway-Maxwell-Poisson, and negative binomial distributions use a log
link by default, but other links can be specified as in
family = poisson(link = "identity"). glmmTMB
provides two parameterizations of the negative binomial which differ in
the dependence of the variance (\(\sigma^2\)) on the mean (\(\mu\)). For family = nbinom1,
the variance increases linearly with the mean as \(\sigma^2 = \mu(1+\alpha)\), with \(\alpha>0\); for
family = nbinom2, the variance increases quadratically with
the mean as \(\sigma^2 =
\mu(1+\mu/\theta)\), with \(\theta>0\) (Hardin and Hilbe 2007). For the
Conway-Maxwell-Poisson distribution, there is no closed form equation
for the variance (Huang 2017).
With the default dispersion model (dispformula = ~ 1),
the dispersion parameter (e.g., \(\alpha\) or \(\theta\) for the negative binomial
distribution) is identical for each observation. Alternatively, the
dispersion parameter can vary with fixed effects; in this case, the
dispersion model uses a log link. The dispersion model can be used to
account for heteroskedasticity. For example, if the response is more
variable (relative to the mean) as the year progresses, then a model
with either negative binomial distribution might use the one-sided
formula dispformula = ~ DOY where DOY is the
day of the year. When the same variables are in the conditional and
dispersion models, the mean-variance relationship can be manipulated,
but this could potentially lead to non-convergence issues. A description
of the dispersion parameter for each distribution can be accessed by
typing ?sigma.glmmTMB in R.
The zero-inflation model describes the probability of observing an
extra (i.e., structural) zero that is not generated by the conditional
model. Zero-inflation creates an extra point mass of zeros in the
response distribution; the overall distribution is a mixture of the
conditional model and zero-inflation model (Lambert 1992; Rhodes 2015). The zero-inflation
probability is bounded between zero and one by using a logit link. For
example, if salamanders emerged seasonally at each site, such that a
structural zero could occur either because a site was contaminated or
because it was visited too early in the season, then the model could
include the one-sided formula ziformula = ~ DOY. The
probability of producing a structural zero can be modeled as equal for
all observations with ziformula = ~ 1. In glmmTMB,
it is possible to include random effects in the conditional and
zero-inflation models, but not the dispersion model.
The package is available from The Comprehensive R Archive Network
(CRAN) via the command install.packages("glmmTMB"). The
current version is 0.2.0. Development versions are available from GitHub
and can be installed using devtools
(Wickham and Chang 2017). Current details
for installing development versions should be accessed on the GitHub
page https://github.com/glmmTMB/glmmTMB.
To illustrate how to use glmmTMB and to compare it to other packages, we applied it to two data sets that are distributed with glmmTMB. Additional code and graphs for these examples can be found in Appendicies A and B.
We demonstrate how to use features of glmmTMB to do
model selection and output model results using a data set of the
abundance of salamanders (Figure 3). They were observed four times at 23
sites in streams, some of which were impacted by coal mining; multiple
species and life stages of salamanders were observed. The data set
contains covariates that may affect the habitat suitability of a site
and the ability of researchers to capture salamanders that inhabit the
site (Price et al. 2016, 2015). Price et al. (2016) analyzed the data using a
Bayesian model with an ecological and a sampling component; abundance
was estimated with a hurdle Poisson model and then observations were
modeled as binomial samples from the abundance.
We fit GLMMs, zero-inflated GLMMs, and hurdle models to the
salamander data with Poisson, Conway-Maxwell-Poisson, and negative
binomial distributions on the conditional model. For simplicity, we
neglected some possible covariates. As a null model, we assumed that
counts varied by species (spp) and randomly by site
(site). We fit models where the mean count additionally
depended on mining status (mined). Our full zero-inflated
GLMMs allowed both the conditional and zero-inflation models to differ
between mined and unmined sites. Full zero-inflated and hurdle negative
binomial GLMMs were fit using the following commands (respectively)
:
zinb = glmmTMB(count~spp * mined + (1|site), zi=~spp * mined,
data=Salamanders, family=nbinom2)
hnb = glmmTMB(count~spp * mined + (1|site), zi=~spp * mined,
data=Salamanders, family=truncated_nbinom2)
As is generally the case for model formulas in R, the *
indicates an interaction plus main effects. We used Akaike information
criteria (AIC) to compare all models via the AICtab
function from the bbmle package (B.
Bolker and Team 2017). For convenience, glmmTMB
reports the log-likelihood of unconverged models as NA and
version 1.0.19 of bbmle puts these models at the bottom of
AIC tables. The code for fitting these models and doing model selection
is presented in Appendix A.
Of the models we considered, the most parsimonious was a
Conway-Maxwell-Poisson GLMM that allowed counts to vary with species,
mining, and their interaction. It did not include zero-inflation, as is
common in abundance models (Warton 2005).
Two zero-inflated negative binomial and one zero-inflated
Conway-Maxwell-Poisson model did not converge. Failed convergence is
typically caused by trying to estimate parameters for which the data do
not contain information. Models that do not converge should not be
considered in model comparison. General model convergence issues are
discussed in
vignette("troubleshooting",package="glmmTMB").
The summary of simple GLMMs from glmmTMB is modeled on the familiar output format of lme4. To demonstrate the extra output from zero-inflation and dispersion models, we present the summary from a more complicated model.
glmmTMB(count ~ mined + (1|site), zi=~mined , disp=~DOY, Salamanders, family=nbinom2)
Following the arguments in the function call above, this model allows the conditional mean to depend on whether or not a site was mined and to vary randomly by site. It allows the number of structural (i.e., extra) zeros to depend on mining. Additionally, it allows the dispersion parameter to depend on the day of the year. This model can be represented by the following set of equations
\[\begin{aligned} \mu &=& E(\texttt{count}|u,\texttt{NSZ}) = \exp( \beta_0 + \beta_\texttt{minedno} + u ),\label{ref:mu}\\ \end{aligned} (\#eq:refmu)\]
\[\begin{aligned} u &\sim& N\left(0,\sigma_u^2\right),\label{ref:u}\\ \end{aligned} (\#eq:refu)\]
\[\begin{aligned} \sigma^2 &=& \hbox{Var}(\texttt{count}|u,\texttt{NSZ}) = \mu(1+\mu/\theta),\label{ref:sigma2}\\ \end{aligned} (\#eq:refsigma2)\]
\[\begin{aligned} \hbox{logit}(p) &=& \beta_0^{(\texttt{zi})}+\beta_\texttt{minedno}^{(\texttt{zi})},\label{ref:p_zi}\\ \end{aligned} (\#eq:refp-zi)\]
\[\begin{aligned} \log(\theta) &=& \beta_0^\texttt{(disp)} + \beta_\texttt{DOY}^\texttt{(disp)}\cdot \texttt{DOY}\label{ref:theta}, \end{aligned} (\#eq:reftheta)\]
where \(u\) is a site specific random effect, NSZ is the event “non-structural zero”, \(p=1-\Pr(\texttt{NSZ})\) is the zero inflation probability, and \(\beta\)’s are regression coefficients with subscript denoting covariate/level (with 0 denoting intercept).
summary(glmmTMB(count~mined+(1|site), zi=~mined , disp=~DOY, Salamanders, family=nbinom2))
#> Family: nbinom2 ( log )
#> Formula: count ~ mined + (1 | site)
#> Zero inflation: ~mined
#> Dispersion: ~DOY
#> Data: Salamanders
#>
#> AIC BIC logLik deviance df.resid
#> 1735 1767 -861 1721 637
#>
#> Random effects:
#>
#> Conditional model:
#> Groups Name Variance Std.Dev.
#> site (Intercept) 0.134 0.366
#> Number of obs: 644, groups: site, 23
#>
#> Conditional model:
#> Estimate Std. Error z value Pr(>|z|)
#> (Intercept) -0.540 0.376 -1.44 0.15
#> minedno 1.424 0.365 3.90 0.000098 ***
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
#>
#> Zero-inflation model:
#> Estimate Std. Error z value Pr(>|z|)
#> (Intercept) 0.256 0.487 0.53 0.5988
#> minedno -2.244 0.745 -3.01 0.0026 **
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
#>
#> Dispersion model:
#> Estimate Std. Error z value Pr(>|z|)
#> (Intercept) 0.0278 0.3177 0.09 0.93
#> DOY -0.3947 0.1537 -2.57 0.01 *
#> ---
#> Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
This summary can be broken down into five sections. The top section
is a general overview containing a description of the model
specification (Family, Formula,
Zero inflation, Dispersion, Data)
and resulting information criteria. The information criteria can only be
compared to models fitted by packages that, like, glmmTMB,
compute the full form of the log-likelihood without dropping constant
terms. The second section describes the variability of the
Random effects. In this model, we only had random effects
in the conditional model (equation @ref(eq:refmu)), but random effects
from the zero-inflation model (equation @ref(eq:refp-zi)) could also
appear here. The estimated variance 0.134 is \(\sigma_u^2\) in equation @ref(eq:refu). The
third section describes the coefficients of the
Conditional model (\(\beta_0\) and \(\beta_\texttt{minedno}\) in equation
@ref(eq:refmu)) including Wald \(Z\)
statistics and \(p\)-values. Apart from
the intercept, the estimates are all contrasts as is standard in
regression models. This model has a log link as stated in the top line
of the summary. The fourth section describes the
Zero-inflation model similarly to the
Conditional model except that this model has a logit link.
The zero-inflation model estimates the probability of an extra zero such
that a positive contrast indicates a higher chance of absence (e.g.
minedno < 0 means fewer absences in sites unaffected by
mining); this is the opposite of the conditional model where a positive
contrast indicates a higher abundance (e.g., minedno > 0
means higher abundances in sites unaffected by mining). The estimates in
this section correspond to \(\beta_0^{(\texttt{zi})}\) and \(\beta_\texttt{minedno}^{(\texttt{zi})}\) in
equation @ref(eq:refp-zi). The last section provides estimated
coefficients from the Dispersion model (equation
@ref(eq:reftheta)), which uses a log link to keep the dispersion
parameter \(\theta\) positive. In
contrast, a model with the default (simple) dispersion model would
report the single dispersion parameter on the natural (rather than log)
scale. To interpret the dispersion parameters of any distribution, see
?sigma.glmmTMB.
The current version of the summary function does not
display uncertainty estimates for the random effects nor for single
dispersion parameters, but confidence intervals can be calculated using
the confint function. See ?confint.glmmTMB for
details. All confidence intervals produced by the current version of the
confint function are Wald intervals, based on the standard
errors calculated using the delta method for the parameter on the scale
of the internal parameterization (which varies by family).
Additional model output using the predict and
simulate functions from glmmTMB is
demonstrated in appendix A (Figures 4, 5, 6, and 7).
Because glmmTMB is the only package that can fit
Conway-Maxwell-Poisson GLMMs, it was not possible to do benchmarking
with the most parsimonious model. Therefore, for benchmarking, we used
the second best model (\(\Delta\)
AIC=0.5 ) which substituted a negative binomial response for the
Conway-Maxwell-Poisson response. We measured the time required to fit
this model using multiple packages. We performed three sets of timing
benchmarks: (1) on simulated data with the same structure as the
original salamander data, (2) on the original data replicated to create
more observations per random effect level and the same number of random
effect levels, (3) on simulated data with increasing numbers of random
effect levels and the same number of observations per random effect
level. Benchmarks were run in parallel using parLapply on a
high performance computing cluster with 12 cores. This performance
should match running on a single core. We used default values for all
packages except with glmmADMB which required an additional
argument (extra.args="-ndi 1000000") to allocate additional
memory. By default, brms runs four MCMC chains while
MCMCglmm runs one, which greatly affects their estimation time.
However, it would be simple to speed up fitting of brms models
by running the chains in parallel. For Bayesian methods, the important
aspect of timing is sampling efficiency (minimum effective samples per
unit time, (Bürkner 2017)), but this is
not compatible with the MLE methods, so we limit our presentation of the
timings of the Bayesian methods.
Benchmarking showed that fitting the negative binomial model to
simulated data with the same structure as the original data was, on
average, equally fast in glmmTMB and INLA, 14
times slower with glmmADMB, 29 times slower with
lme4, and 190 times slower with brms.
mgcv fit the model the fastest, taking 0.03 times as long as
glmmTMB. gamlss took 0.24 times as long as
glmmTMB. With increasing numbers of observations, the
estimation times of all packages appeared to follow power law functions
(Figure 1). For simulated data sets with increasing numbers of random
effect levels, estimation time increased as a power-law function for all
packages except INLA which had estimation times that
accelerated (Figure 2). The speed of glmmTMB for models
with more random effect levels is due to the sparseness handling by
TMB. Benchmarking nuances such as memory usage and how
timings scale with model complexity could be investigated in more detail
in future studies.
glmmadmb,glmmTMB,inla,
glmer.nb, and gam was recorded. That model can
be represented as
glmmTMB(count ~ spp * mined + (1 | site), Salamanders, family="nbinom2").
All models had the same number of parameters including random effect
levels. Lines represent linear models fit on the log-log scale. With
increasing numbers of observations (\(n\)), estimation times increased as a
power-law function (\(n^x\)) with
exponents (\(x\)) reported next to
model names.glmmTMB(count ~ spp * mined + (1 | site), Salamanders, family="nbinom2").
The time required to fit the same model using functions
glmmadmb, glmmTMB, inla,
glmer.nb, and gam was recorded. Each simulated
data set had the same number of observations per random effect level —
the same ratio as in the original data. Lines represent linear models
fit on the log-log scale.With increasing numbers of random effect levels
(\(n\)), estimation times increased as
a power-law function (\(n^x\)), except
for INLA which accelerates. The exponents (\(x\)) are reported here as labels over the
lines.To further compare R packages for fitting zero-inflated GLMMs, we analyzed counts of begging behavior by owl nestlings. The full analyses can be found in Appendix B. This example previously appeared in (Zuur et al. 2009) and (Benjamin M. Bolker et al. 2013) and was originally published by (Roulin and Bersier 2007). We compared the estimates of fixed effects and the amount of time required for fitting the same model in INLA, MCMCglmm, glmmADMB, mgcv, and brms (HRue, Martino, and Chopin 2009; Hadfield 2010; Skaug et al. 2012; Wood, Pya, and Säfken 2016; Bürkner 2017). For brms and MCMCglmm, we used the default number of iterations, burn-in samples, and thinning. In each package, we fit zero-inflated Poisson models with six fixed effects, one random effect; we also accounted for overdispersion, although sometimes (of necessity) in slightly different ways with different packages (e.g., negative binomial vs. log-normal-Poisson models). We allowed zero-inflation to vary with food treatment and vary randomly with nest. See Appendix B for details of these methods, including code.
Estimates and confidence (or credible) intervals (CI) from
brms, mgcv, MCMCglmm, and INLA
were nearly identical to those of glmmTMB, when running the
Bayesian models with flat priors (Figures 8 and 9).
We have introduced an R package that can quickly estimate a variety of models including GLMs, GLMMs, zero-inflated GLMMs, and hurdle models. By providing this flexibility in a single package, we reduce the need for researchers to learn multiple packages. Another benefit is that models estimated with a single package can be compared using likelihood-based methods including information criteria. Using information criteria to select a model for the salamander data, we found that (among the models we considered) zero-inflation did not improve the fit; we expect that this will be a common result. While glmmTMB allows users to easily fit complicated models, a maximally complex model might not be necessary and might not converge, as we saw here. Other packages have many of the features implemented in glmmTMB, but none have the ability to fit Conway-Maxwell-Poisson GLMMs. Overall, glmmTMB is a very flexible package for modeling count data with zero-inflated GLMMs while still ranking highly in speed comparisons.
Thanks to S Price for providing the data on salamanders and for helpful comments on the manuscript. Thanks to P-C Bürkner, J Hadfield, M Bekker-Nielsen Dunbar, and two anonymous reviewers for helpful comments on the manuscript. Thanks to A Zuur for providing the data on owl nestlings. Thanks to G Simpson for advice on capabilities of the mgcv package. This work was supported by grants from the Swiss National Science Foundation (#IZ320Z0_161670) and from the AD Model Builder Foundation to MEB.
In this appendix, we reanalyze counts of salamanders in streams. Repeated samples of salamanders were taken at 23 sites. Some of the sites were affected by mountain top removal coal mining. The data was originally published in (Price et al. 2016) and was acquired from Dryad (Price et al. 2015). These analyses are intended to be a simple demonstration of how to use some features of the glmmTMB package, so we do not attempt to fit all of the models that could be reasonable to try with the covariates that were collected.
The syntax for fitting GLMMs with glmmTMB is quite similar
to using glmer. In the first model, the formula,
count ~ spp + (1 | site), says that counts depend on
species and vary randomly by site. We also pass it the data frame,
Salamanders, and specify a Poisson distribution using the
family argument. glmmTMB assumes that we want a
log link with the Poisson distribution because that’s the standard.
pm0 = glmmTMB(count~spp + (1|site), Salamanders, family=poisson)
pm1 = glmmTMB(count~spp + mined + (1|site), Salamanders, family=poisson)
pm2 = glmmTMB(count~spp * mined + (1|site), Salamanders, family=poisson)
To fit Conway-Maxwell-Poisson models, we use
family=compois instead of poisson.
cmpm0 = glmmTMB(count~spp + (1|site), Salamanders, family=compois)
cmpm1 = glmmTMB(count~spp + mined + (1|site), Salamanders, family=compois)
cmpm2 = glmmTMB(count~spp * mined + (1|site), Salamanders, family=compois)
nbm0 = glmmTMB(count~spp + (1|site), Salamanders, family=nbinom2)
nbm1 = glmmTMB(count~spp + mined + (1|site), Salamanders, family=nbinom2)
nbm2 = glmmTMB(count~spp * mined + (1|site), Salamanders, family=nbinom2)
Unlike the Poisson, the negative binomial distribution has a
dispersion parameter. If we expected the counts to become more dispersed
(relative to the mean) as the year progresses, then we could use the
dispersion formula to model how the dispersion changes with the day of
the year (DOY) using disp= ~ DOY.
nbdm0 = glmmTMB(count~spp + (1|site), disp=~DOY, Salamanders, family=nbinom2)
nbdm1 = glmmTMB(count~spp + mined + (1|site), disp=~DOY, Salamanders, family=nbinom2)
nbdm2 = glmmTMB(count~spp * mined + (1|site), disp=~DOY, Salamanders, family=nbinom2)
To fit zero-inflated models, we use the ziformula
argument, or glmmTMB will also recognize zi. This
is a formula that describes how the probability of an extra zero (i.e.,
structural zero) will vary with predictors. In this example, we might
assume that absences will at least vary by species (spp),
so we write zi= ~ spp. This formula only has a right side
because the left side is always the probability of having a structural
zero in the response that was specified in the first formula. The
zero-inflation probability is always modeled with a logit link to keep
it between 0 and 1.
Zero-inflation can be used with any of the distributions in glmmTMB, so we compare the same conditional and zero-inflation models with Poisson, Conway-Maxwell-Poisson, and negative binomial distributions.
Warning messages tell us that zicmpm3,
zinbm0, and zinbm1 do not converge. The
convergence warning refers to vignette("troubleshooting");
this vignette will expand as advice for troubleshooting convergence
issues develops. It seems that zicmpm3 is
overparameterized, but the problem with zinbm0 and
zinbm1 is that they only have mined in the
conditional model and not the zero-inflation model, so that they do not
agree well with the data. Plotting the data and thinking carefully about
the models should help to avoid convergence issues.
zipm0 = glmmTMB(count~spp +(1|site), zi=~spp, Salamanders, family=poisson)
zipm1 = glmmTMB(count~spp + mined +(1|site), zi=~spp, Salamanders, family=poisson)
zipm2 = glmmTMB(count~spp + mined +(1|site), zi=~spp + mined, Salamanders, family=poisson)
zipm3 = glmmTMB(count~spp * mined +(1|site), zi=~spp * mined, Salamanders, family=poisson)
zicmpm0 = glmmTMB(count~spp +(1|site), zi=~spp, Salamanders, family=compois)
zicmpm1 = glmmTMB(count~spp + mined +(1|site), zi=~spp, Salamanders, family=compois)
zicmpm2 = glmmTMB(count~spp + mined +(1|site), zi=~spp + mined, Salamanders, family=compois)
zicmpm3 = glmmTMB(count~spp * mined +(1|site), zi=~spp * mined, Salamanders, family=compois)
#> Warning in fitTMB(TMBStruc): Model convergence problem; non-positive-
#> definite Hessian matrix. See vignette('troubleshooting')
zinbm0 = glmmTMB(count~spp +(1|site), zi=~spp, Salamanders, family=nbinom2)
#> Warning in fitTMB(TMBStruc): Model convergence problem; non-positive-
#> definite Hessian matrix. See vignette('troubleshooting')
zinbm1 = glmmTMB(count~spp + mined +(1|site), zi=~spp, Salamanders, family=nbinom2)
#> Warning in fitTMB(TMBStruc): Model convergence problem; non-positive-
#> definite Hessian matrix. See vignette('troubleshooting')
zinbm2 = glmmTMB(count~spp + mined +(1|site), zi=~spp + mined, Salamanders, family=nbinom2)
zinbm3 = glmmTMB(count~spp * mined +(1|site), zi=~spp * mined, Salamanders, family=nbinom2)
#> Warning in fitTMB(TMBStruc): Model convergence problem; singular
#> convergence (7). See vignette('troubleshooting')
We can also fit hurdle models in a single model by using a truncated distribution for the conditional model and adding zero-inflation.
hpm0 = glmmTMB(count~spp + (1|site), zi=~spp, Salamanders, family=truncated_poisson)
hpm1 = glmmTMB(count~spp + mined + (1|site), zi=~spp + mined, Salamanders,
family=truncated_poisson)
hpm2 = glmmTMB(count~spp * mined + (1|site), zi=~spp + mined, Salamanders,
family=truncated_poisson)
hnbm0 = glmmTMB(count~spp + (1|site), zi=~spp, Salamanders, family=truncated_nbinom2)
hnbm1 = glmmTMB(count~spp + mined + (1|site), zi=~spp + mined, Salamanders,
family=truncated_nbinom2)
hnbm2 = glmmTMB(count~spp * mined + (1|site), zi=~spp + mined, Salamanders,
family=truncated_nbinom2)
We can use AICtab to compare all the GLMMs, including
zero-inflated and hurdle models. Here, to save space, we only output the
AICtable for the top four and bottom four models. The most parsimonious
model has a Conway-Maxwell-Poisson distribution with effects of species,
mining, and their interaction.
AICtab(pm0, pm1, pm2,
cmpm0, cmpm1, cmpm2,
nbm0, nbm1, nbm2,
nbdm0, nbdm1, nbdm2,
zipm0, zipm1, zipm2, zipm3,
zicmpm0, zicmpm1, zicmpm2, zicmpm3,
zinbm0, zinbm1, zinbm2, zinbm3,
hpm0, hpm1, hpm2,
hnbm0, hnbm1, hnbm2)
The top of the table
| model | df | dAIC |
|---|---|---|
| cmpm2 | 16 | 0.00 |
| nbm2 | 16 | 0.48 |
| nbdm2 | 17 | 1.99 |
| zicmpm2 | 18 | 2.09 |
| zinbm3 | 30 | 6.80 |
and the bottom
| model | df | dAIC |
|---|---|---|
| hpm0 | 15 | 314 |
| pm0 | 8 | 330 |
| zicmpm3 | 30 | NA |
| zinbm0 | 16 | NA |
| zinbm1 | 17 | NA |
The log-likelihood of the unconverged models is reported as
NA so that these models appear at the end of the AIC table.
The negative log-likelihood could be extracted with
zinbm1$fit$objective if it was needed.
There are many decisions to make about marginalizing over or conditioning on the random effects. See discussion at https://cran.r-project.org/web/packages/merTools/vignettes/Using_predictInterval.html.
For demonstration purposes, we plot results from the top
zero-inflated model zinbm3.
It’s easiest to see the pattern by using the predict
function. To avoid marginalizing over or conditioning on random effects,
we can refit the best model without the random effect of site; however,
this is not ideal because it ignores the correlation within sites. We
present a more rigorous version next.
The predict function has a parameter zitype
that specifies whether you want predictions from the conditional model,
the zero-inflation model, or the expected response that combines both
parts of the model.
zinbm3FE = glmmTMB(count~spp * mined, zi=~spp * mined, Salamanders, family=nbinom2)
newdata0 = newdata = unique(Salamanders[,c("mined","spp")])
temp = predict(zinbm3FE, newdata, se.fit=TRUE, zitype="response")
newdata$predFE = temp$fit
newdata$predFE.min = temp$fit-1.96*temp$se.fit
newdata$predFE.max = temp$fit+1.96*temp$se.fit
real=ddply(Salamanders, ~site+spp+mined, summarize, m=mean(count))
ggplot(newdata, aes(spp, predFE, colour=mined))+geom_point()+
geom_errorbar(aes(ymin=predFE.min, ymax=predFE.max))+
geom_point(data=real, aes(x=spp, y=m) )+
ylab("Average abundance \n including presences and absences")+
xlab("Species")
We can predict at the population mode, by setting the random effects to zero.
X.cond = model.matrix(lme4::nobars(formula(zinbm3)[-2]), newdata0)
beta.cond = fixef(zinbm3)$cond
pred.cond = X.cond %*% beta.cond
ziformula = zinbm3$modelInfo$allForm$ziformula #$
X.zi = model.matrix(lme4::nobars(ziformula), newdata0)
beta.zi = fixef(zinbm3)$zi
pred.zi = X.zi %*% beta.zi
These are estimates of the linear predictors (i.e., predictions on the link scale: logit(prob) and log(cond)), not the predictions themselves. The easiest thing to do for the point estimates of the unconditional count (ucount) is to transform to the response scale and multiply:
pred.ucount = exp(pred.cond)*(1-plogis(pred.zi))
For the standard errors/confidence intervals, we could use posterior predictive simulations (i.e., draw multivariate normal samples from the parameter for the fixed effects). This conditions on/ignores uncertainty in the random-effect parameters.
library(MASS)
set.seed(101)
pred.condpar.psim = mvrnorm(1000,mu=beta.cond,Sigma=vcov(zinbm3)$cond)
pred.cond.psim = X.cond %*% t(pred.condpar.psim)
pred.zipar.psim = mvrnorm(1000,mu=beta.zi,Sigma=vcov(zinbm3)$zi)
pred.zi.psim = X.zi %*% t(pred.zipar.psim)
pred.ucount.psim = exp(pred.cond.psim)*(1-plogis(pred.zi.psim))
ci.ucount = t(apply(pred.ucount.psim,1,quantile,c(0.025,0.975)))
ci.ucount = data.frame(ci.ucount)
names(ci.ucount) = c("ucount.low","ucount.high")
pred.ucount = data.frame(newdata0, pred.ucount, ci.ucount)
These predicted counts should be close to the median counts, so we plot them together to compare.
real.count = ddply(Salamanders, ~spp+mined, summarize, m=median(count), mu=mean(count))
ggplot(pred.ucount, aes(x=spp, y=pred.ucount, colour=mined))+geom_point(shape=1, size=2)+
geom_errorbar(aes(ymin=ucount.low, ymax=ucount.high))+
geom_point(data=real.count, aes(x=spp, y=m, colour=mined), shape=0, size=2)+
geom_point(data=real.count, aes(x=spp, y=mu, colour=mined), shape=5, size=2)+
ylab("Abundance \n including presences and absences")+
xlab("Species")
We could also examine the distribution of simulated values from the
best fitted model. For this we use the function
simulate.glmmTMB. This function works for zero-inflated and
hurdle models as well as less complex models.
sims=simulate(nbm2, seed = 1, nsim = 1000)
This function returns a list of vectors. The list has one element for
each simulation (nsim) and the vectors are the same shape
as our response variable.
simdatlist=lapply(sims, function(count){
cbind(count, Salamanders[,c('site', 'mined', 'spp')])
})
simdatsums=lapply(simdatlist, function(x){
ddply(x, ~spp+mined, summarize,
absence=mean(count==0),
mu=mean(count))
})
ssd=do.call(rbind, simdatsums)
Then we can plot them with the observations summarized in the same way.
real = ddply(Salamanders, ~spp+mined, summarize,
absence=mean(count==0),
mu=mean(count))
ggplot(ssd, aes(x=absence, color=mined))+
geom_density(adjust=4)+
facet_wrap(~spp)+
geom_point(data=real, aes(x=absence, y=1, color=mined), size=2)+
xlab("Probability that salamanders are not observed")+ylab(NULL)
We can see that this model does a good job of capturing the observed zero counts.
ggplot(ssd, aes(x=mu, color=mined))+
geom_density(adjust=4)+
facet_wrap(~spp)+
geom_point(data=real, aes(x=mu, y=.5, color=mined), size=2)+
xlab("Abundance including presences and absences")+ylab(NULL)
In this appendix, we analyze counts of begging behavior by owl
nestlings. This example previously appeared in similar forms (Zuur et al. 2009) and (Benjamin M. Bolker et al. 2013); the data were
originally published by (Roulin and Bersier
2007). The response variable is the number of calls from chicks
(NCalls) in a nest. Two changes from the example published
in (Benjamin M. Bolker et al. 2013) are
that (1) we use an observation-level random effect to account for
overdispersion; (2) instead of assuming that the number of calls is
strictly proportional to brood size (i.e., using an offset of log(brood
size)), we fit the model with log(brood size) as a predictor, equivalent
to assuming that \(\textrm{calls} \propto
(\textrm{brood size})^\gamma\), with \(\gamma\) not necessarily equal to 1.
Since nests were repeatedly measured, Nest is included
as a random effect; observation-level random effects are incorporated to
allow for overdispersion (Elston et al. 2001;
Hadfield 2010). Covariates of interest include the sex of the
parent visiting the nest (SexParent), whether the chicks
were satiated or not (FoodTreatment), and the timing of the
parent’s arrival (ArrivalTime).
library(glmmTMB)
library(glmmADMB)
library(MCMCglmm)
library(brms)
library(INLA)
library(mgcv)
library(broom) #for tidy devtools::install_github("bbolker/broom")
library(plyr)
library(dplyr) #tidyverse
library(ggplot2); theme_set(theme_bw())
library(ggstance)#for position_dodgev
Here we fit the model with zero-inflation assumed to be constant across the data set, i.e., zero-inflation is independent of the predictor variables.
fixef1 = NCalls~(FoodTreatment + ArrivalTime) * SexParent + logBroodSize
form1 = update(fixef1, . ~ . + (1|Nest)+(1|obs))
time.tmb = tfun(m1.tmb <<- glmmTMB(form1,
ziformula=~1, data = Owls,
family=poisson))
With the additions to the model (logBroodSize as a
covariate and observation-level random effects), we were unsuccessful in
fitting the model with glmmADMB. Some variants (e.g., with
observation-level random effects, but with logBroodSize as
an offset) were possible by modifying control settings (i.e.
admb.opts=admbControl(shess=FALSE,noinit=FALSE)), but even
when successful these fits were very slow (>10 minutes).
Code for this example was modified from (Benjamin M. Bolker et al. 2013); a more complete description appears in the supplementary material for that paper.
fixef2 = NCalls~trait-1+ # intercept terms for both count and binary terms
# other fixed-effect terms only apply to count term
at.level(trait,1):logBroodSize+
at.level(trait,1):((FoodTreatment+ArrivalTime)*SexParent)
nfix = 8
# residual variances independent for count and binary terms;
# fixed to 1 for binary term
# random-effects variances independent for count and binary terms;
# fixed very small (1e-6) for binary term
prior_overdisp = list(R=list(V=diag(c(1,1)),nu=0.002,fix=2),
G=list(list(V=diag(c(1,1e-6)),nu=0.002,fix=2)))
prior_overdisp_broodoff = c(prior_overdisp,
list(B=list(mu=rep(0,nfix),
V=diag(rep(1e4,nfix)))))
set.seed(101)
time.MCMCglmm = tfun(m1.MCMCglmm <<- MCMCglmm(fixef2,
rcov=~idh(trait):units,
random=~idh(trait):Nest,
prior=prior_overdisp_broodoff,
data=Owls,
nitt=103000,
thin=100,
family="zipoisson",
verbose=FALSE))
We adjusted the number of samples until the effective sample size of the most poorly sampled parameter (the zero-inflation parameter, in this case) was greater than 500; with 100,000 samples after a burn-in of 3,000, we achieved a minimum effective sample size of 568 (for the zero-inflation parameter).
time.brms = tfun(m1.brms <<- brm(form1, data = Owls,
iter=1000,
family="zero_inflated_poisson"))
#> Compiling the C++ model
#> Start sampling
One of the known advantages of Hamiltonian Monte Carlo, as implemented in Stan (on which brms is built), is that it achieves high effective sample size per MCMC step; we were able to cut down the number of samples considerably from the default of 2000 and still achieve a minimum effective sample size of approximately 500 (the minimum effective sample size achieved was 460).
We resample to estimate the time required for sampling only (i.e., not including model compilation
time.brms2 = tfun(m1.brms2 <<- update(m1.brms))
#> Start sampling
form2 = update(fixef1, . ~ . + f(Nest, model="iid") + f(obs, model="iid"))
time.inla = tfun(m1.inla <<-
inla(form2,
family= "zeroinflatedpoisson1",
data=Owls))
To the best of our knowledge, mgcv::gam is currently
unable to fit models with the combination of zero-inflation and
overdispersion (the ziplss() famiy that handles
zero-inflation handles only a ZIP case rather than zero-inflated
negative binomial or other extensions, and observation-level random
effects cannot be fit with gam’s random-effect approach).
To address this issue, we fitted a GAM with zero-inflated Poisson
responses and used a quasi-likelihood approach: i.e., estimating
overdispersion as \[sum of squared Pearson
residuals/residual degrees of freedom\] and inflating the
parameter standard errors by the square root of the overdispersion.
form3 = update(fixef1, . ~ . + s(Nest, bs="re"))
time.mgcv = tfun(m1.gam <<- gam(list(form3, ~ 1),
data = Owls,
family = ziplss(), method = "REML"))
Timings:
| time (sec) | |
|---|---|
| mgcv | 0.2 |
| glmmTMB | 2.5 |
| INLA | 4.2 |
| MCMCglmm | 53.0 |
| brms (no compilation) | 55.2 |
| brms (with compilation) | 115.6 |
The deterministic methods (gam, glmmTMB and
inla) were all fast; gam was fastest, because
we fitted a simpler model (see above). The stochastic methods
(MCMCglmm and brm) were about an order of
magnitude slower.
glmmTMB, MCMCglmm, brm,
inla, and gam.Because we ran brms with flat priors, the estimates are very
close to the ML estimates of glmmTMB. The most different
results are from gam, because we used a quasi-likelihood
model with a slightly different implicit variance scaling.
Here we fit the model with zero-inflation depending on some of the predictor variables. We can no longer use glmmADMB or INLA (INLA allows the zero-inflation probabilities to depend on covariates in hurdle models — “type 0” in the INLA documentation — but not for zero-inflated models).
form0 = update(fixef1, . ~ . + (1|Nest))
ziform = ~FoodTreatment+(1|Nest)
time.tmb_czi = tfun(m1.tmb_czi <<- glmmTMB(form0,
ziformula=ziform,
data = Owls, family=nbinom2))
Attempting to fit the glmmTMB model with a log Normal-Poisson model (i.e., a Poisson model with observation-level random effects) and covariate-dependent zero-inflation led to convergence failure, so we substituted a similar model (a negative-binomial model without observation-level random effects).
fixef3 = NCalls~trait-1+ # intercept terms for both count and binary terms
# fixed-effect terms for count term
at.level(trait,1):logBroodSize+
at.level(trait,1):((FoodTreatment+ArrivalTime)*SexParent)+
# fixed-effect terms for binary term
at.level(trait,2):FoodTreatment
nfix = 9
# residual variances independent for count and binary terms;
# fixed to 1 for binary term
# random-effects variances now allow estimated variance for binary term
# as well
prior_overdisp_czi = list(R=list(V=diag(c(1,1)),nu=0.002,fix=2),
G=list(list(V=diag(c(1,1)),nu=0.002)))
prior_overdisp_broodoff_czi = c(prior_overdisp_czi,
list(B=list(mu=rep(0,nfix),
V=diag(rep(1e4,nfix)))))
set.seed(101)
time.mcmc_czi=tfun(m1.mcmc_czi <<- MCMCglmm(fixef3,
rcov=~idh(trait):units,
random=~idh(trait):Nest,
prior=prior_overdisp_broodoff_czi,
data=Owls,
nitt=153000,
family="zipoisson",
verbose=FALSE))
## warning message suppressed ...
Minimum effective sample size: 884
time.brms_czi = tfun(m1.brms_czi <<- brm(brmsformula(form1, zi=ziform),
data = Owls,
family="zero_inflated_poisson"))
#> Compiling the C++ model
#> Start sampling
time.brms_czi2 = tfun(m1.brms_czi2 <<- update(m1.brms_czi))
#> Start sampling
time.mgcv_czi = tfun(m1.gam_czi <<- gam(list(form3,
~FoodTreatment+ s(Nest, bs = "re")),
data = Owls, family = ziplss(), method = "REML"))
Timings:
| time (sec) | |
|---|---|
| mgcv | 0.3 |
| TMB | 3.9 |
| brms (no compilation) | 53.1 |
| MCMCglmm | 88.5 |
| brms (with compilation) | 174.4 |
glmmTMB,
MCMCglmm, brm, and gam.Package versions:
#> brms glmmADMB glmmTMB INLA MCMCglmm mgcv
#> 1.10.2 0.8.5 0.2.0 17.6.20 2.25 1.8.20