# Estimating Generalized Linear Models for Count Data with rstanarm

#### Jonah Gabry and Ben Goodrich

#### 2016-11-20

# Introduction

This vignette explains how to estimate generalized linear models (GLMs) for count data using the `stan_glm` function in the rstanarm package.

The four steps of a Bayesian analysis are

1. Specify a joint distribution for the outcome(s) and all the unknowns, which typically takes the form of a marginal prior distribution for the unknowns multiplied by a likelihood for the outcome(s) conditional on the unknowns. This joint distribution is proportional to a posterior distribution of the unknowns conditional on the observed data
2. Draw from posterior distribution using Markov Chain Monte Carlo (MCMC).
3. Evaluate how well the model fits the data and possibly revise the model.
4. Draw from the posterior predictive distribution of the outcome(s) given interesting values of the predictors in order to visualize how a manipulation of a predictor affects (a function of) the outcome(s).

Steps 3 and 4 are covered in more depth by the vignette entitled “How to Use the rstanarm Package”. This vignette focuses on Step 1 for Poisson and negative binomial regression models using the `stan_glm` function.

# Likelihood

If the outcome for a single observation \(y\) is assumed to follow a Poisson distribution, the likelihood for one observation can be written as a conditionally Poisson PMF

\[\tfrac{1}{y!} \lambda^y e^{-\lambda},\]

where \(\lambda = E(y | \mathbf{x}) = g^{-1}(\eta)\) and \(\eta = \alpha + \mathbf{x}^\top \boldsymbol{\beta}\) is a linear predictor. For the Poisson distribution it is also true that \(\lambda = Var(y | \mathbf{x})\), i.e. the mean and variance are both \(\lambda\). Later in this vignette we also show how to estimate a negative binomial regression, which relaxes this assumption of equal conditional mean and variance of \(y\).

Because the rate parameter \(\lambda\) must be positive, for a Poisson GLM the link function \(g\) maps between the positive real numbers \(\mathbb{R}^+\) (the support of \(\lambda\)) and the set of all real numbers \(\mathbb{R}\). When applied to a linear predictor \(\eta\) with values in \(\mathbb{R}\), the inverse link function \(g^{-1}(\eta)\) therefore returns a positve real number.

Although other link functions are possible, the canonical link function for a Poisson GLM is the log link \(g(x) = \ln{(x)}\). With the log link, the inverse link function is simply the exponential function and the likelihood for a single observation becomes

\[\frac{g^{-1}(\eta)^y}{y!} e^{-g^{-1}(\eta)} = \frac{e^{\eta y}}{y!} e^{-e^\eta}.\]

# Priors

A full Bayesian analysis requires specifying prior distributions \(f(\alpha)\) and \(f(\boldsymbol{\beta})\) for the intercept and vector of regression coefficients. When using `stan_glm`, these distributions can be set using the `prior_intercept` and `prior` arguments. The `stan_glm` function supports a variety of prior distributions, which are explained in the rstanarm documentation (`help(priors, package = 'rstanarm')`).

As an example, suppose we have \(K\) predictors and believe — prior to seeing the data — that \(\alpha, \beta_1, \dots, \beta_K\) are as likely to be positive as they are to be negative, but are highly unlikely to be far from zero. These beliefs can be represented by normal distributions with mean zero and a small scale (standard deviation). To give \(\alpha\) and each of the \(\beta\)s this prior (with a scale of 1, say), in the call to `stan_glm` we would include the arguments `prior_intercept = normal(0,1)` and `prior = normal(0,1)`.

If, on the other hand, we have less a priori confidence that the parameters will be close to zero then we could use a larger scale for the normal distribution and/or a distribution with heavier tails than the normal like the Student t distribution. Step 1 in the “How to Use the rstanarm Package” vignette discusses one such example.

# Posterior

With independent prior distributions, the joint posterior distribution for \(\alpha\) and \(\boldsymbol{\beta}\) in the Poisson model is proportional to the product of the priors and the \(N\) likelihood contributions:

\[f\left(\alpha,\boldsymbol{\beta} | \mathbf{y},\mathbf{X}\right) \propto f\left(\alpha\right) \times \prod_{k=1}^K f\left(\beta_k\right) \times \prod_{i=1}^N { \frac{g^{-1}(\eta_i)^{y_i}}{y_i!} e^{-g^{-1}(\eta_i)}}.\]

This is posterior distribution that `stan_glm` will draw from when using MCMC.

# Poisson and Negative Binomial Regression Example

This example comes from Chapter 8.3 of Gelman and Hill (2007).

We want to make inferences about the efficacy of a certain pest management system at reducing the number of roaches in urban apartments. Here is how Gelman and Hill describe the experiment (pg. 161):

> […] the treatment and control were applied to 160 and 104 apartments, respectively, and the outcome measurement \(y_i\) in each apartment \(i\) was the number of roaches caught in a set of traps. Different apartments had traps for different numbers of days […]

In addition to an intercept, the regression predictors for the model are the pre-treatment number of roaches `roach1`, the treatment indicator `treatment`, and a variable indicating whether the apartment is in a building restricted to elderly residents `senior`. Because the number of days for which the roach traps were used is not the same for all apartments in the sample, we include it as an exposure, which slightly changes the model described in the Likelihood section above in that the rate parameter \(\lambda_i = exp(\eta_i)\) is multiplied by the exposure \(u_i\) giving us \(y_i \sim Poisson(u_i \lambda_i)\). This is equivalent to adding \(\ln{(u_i)}\) to the linear predictor \(\eta_i\) and it can be specified using the `offset` argument to `stan_glm`.

    library(rstanarm)
    data(roaches)

    # Rescale
    roaches$roach1 <- roaches$roach1 / 100
    # Estimate original model
    glm1 <- glm(y ~ roach1 + treatment + senior, offset = log(exposure2),
                data = roaches, family = poisson)
    # Estimate Bayesian version with stan_glm
    stan_glm1 <- stan_glm(y ~ roach1 + treatment + senior, offset = log(exposure2),
                          data = roaches, family = poisson,
                          prior = normal(0,2.5), prior_intercept = normal(0,5),
                          chains = CHAINS, cores = CORES, seed = SEED)

The `formula`, `data`, `family`, and `offset` arguments to `stan_glm` can be specified in exactly the same way as for `glm`. The `poisson` family function defaults to using the log link, but to write code readable to someone not familiar with the defaults we should be explicit and use `family = poisson(link = "log")`.

We’ve also specified some optional arguments. The `chains` argument controls how many Markov chains are executed, the `cores` argument controls the number of cores utilized by the computer when fitting the model. We also provided a seed so that we have the option to deterministically reproduce these results at any time. The `stan_glm` function has many other optional arguments that allow for more user control over the way estimation is performed. The documentation for `stan_glm` has more information about these controls as well as other topics related to GLM estimation.

Here are the point estimates and uncertainties from the `glm` fit and `stan_glm` fit, which we see are nearly identical:

    round(rbind(glm = coef(glm1), stan_glm = coef(stan_glm1)), digits = 2)

             (Intercept) roach1 treatment senior
    glm             3.09    0.7     -0.52  -0.38
    stan_glm        3.09    0.7     -0.52  -0.38

    round(rbind(glm = summary(glm1)$coefficients[, "Std. Error"],
                stan_glm = se(stan_glm1)), digits = 3)

             (Intercept) roach1 treatment senior
    glm            0.021  0.009     0.025  0.033
    stan_glm       0.020  0.009     0.022  0.032

(Note: the dataset we have is slightly different from the one used in Gelman and Hill (2007), which leads to slightly different parameter estimates than those shown in the book even when copying the `glm` call verbatim. Also, we have rescaled the `roach1` predictor. For the purposes of this example, the actual estimates are less important than the process.)

Gelman and Hill next show how to compare the observed data to replicated datasets from the model to check the quality of the fit. Here we don’t show the original code used by Gelman and Hill because it’s many lines, requiring several loops and some care to get the matrix multiplications right (see pg. 161-162). On the other hand, the rstanarm package makes this easy. We can generate replicated datasets with a single line of code using the `posterior_predict` function:

    yrep <- posterior_predict(stan_glm1)

By default `posterior_predict` will generate a dataset for each set of parameter draws from the posterior distribution. That is, `yrep` will be an \(S \times N\) matrix, where \(S\) is the size of the posterior sample and \(N\) is the number of data points. Each row of `yrep` represents a full dataset generated from the posterior predictive distribution. For more about the importance of the `posterior_predict` function, see the “How to Use the rstanarm Package” vignette.

Gelman and Hill take the simulated datasets and for each of them compute the proportion of zeros and compare to the observed proportion in the original data. We can do this easily using the `pp_check` function, which generates graphical comparisons of the data `y` and replicated datasets `yrep`.

    prop_zero <- function(y) mean(y == 0)
    (prop_zero_test1 <- pp_check(stan_glm1, plotfun = "stat", stat = "prop_zero"))

The value of the test statistic (in this case the proportion of zeros) computed from the sample `y` is the vertical blue line. More than 30% of these observations are zeros, whereas the replicated datasets all contain less than 1% zeros. This is a sign that we should consider a model that more accurately accounts for the large proportion of zeros in the data. Gelman and Hill show how we can do this using an overdispered Poisson regression. To illustrate the use of a different `stan_glm` model, here we will instead try negative binomial regression, which is also used for overdispersed or zero-inflated count data. The negative binomial distribution allows the (conditional) mean and variance of \(y\) to differ unlike the Poisson distribution. To fit the negative binomial model can either use the `stan_glm.nb` function or, equivalently, change the `family` we specify in the call to `stan_glm` to `neg_binomial_2` instead of `poisson`. To do the latter we can just use `update`:

    stan_glm2 <- update(stan_glm1, family = neg_binomial_2)

We now use `pp_check` again, this time to check the proportion of zeros in the replicated datasets under the negative binomial model:

    library(gridExtra)
    prop_zero_test2 <- pp_check(stan_glm2, plotfun = "stat", stat = "prop_zero")
    # Show graphs for Poisson and negative binomial side by side
    grid.arrange(prop_zero_test1 + ggtitle("Poisson"),
                 prop_zero_test2 + ggtitle("Negative Binomial"),
                 ncol = 2)

This is a much better fit, as the proportion of zeros in the data falls nicely near the center of the distribution of the proportion of zeros among the replicated datasets. The observed proportion of zeros is quite plausible under this model.

We could have also made these plots manually without using the `pp_check` function because we have the `yrep` datasets created by `posterior_predict`. The `pp_check` function takes care of this for us, but `yrep` can be used directly to carry out other posterior predictive checks that aren’t automated by `pp_check`.

When we comparing the models using the loo package we also see a clear preference for the negative binomial model

    loo1 <- loo(stan_glm1)
    loo2 <- loo(stan_glm2)
    compare(loo1, loo2)

    elpd_diff        se
       5351.3     709.5

which is not surprising given the better fit we’ve already observed from the posterior predictive checks.

# References

Gelman, A. and Hill, J. (2007). Data Analysis Using Regression and Multilevel/Hierarchical Models. Cambridge University Press, Cambridge, UK.