STA 602L Lab 3: The Poisson model and posterior predictive checks

STA 602L: Bayesian and Modern Statistics

Feb 3, 2020

Due: 11:59pm, Feb 3, 2020

Housekeeping

R/RStudio

You all should have R and RStudio installed on your computers by now. If you do not, first install the latest version of R here: https://cran.rstudio.com (remember to select the right installer for your operating system). Next, install the latest version of RStudio here: https://www.rstudio.com/products/rstudio/download/. Scroll down to the “Installers for Supported Platforms” section and find the right installer for your operating system.

R Markdown

You are required to use R Markdown to type up this lab report. If you do not already know how to use R markdown, here is a very basic R Markdown template: https://sta-602l-s20.github.io/Course-Website/labs/resources/LabReport.Rmd. Refer to the resources tab of the course website (here: https://sta-602l-s20.github.io/Course-Website/resources/ ) for links to help you learn how to use R markdown.

Gradescope

You MUST submit both your .Rmd and .pdf files to the course site on Gradescope here: https://www.gradescope.com/courses/77790/assignments. Make sure to knit to pdf and not html; ask the TA about knitting to pdf if you cannot figure it out. Be sure to submit under the right assignment entry.

Getting started

You will need the following R packages. If you do not already have them installed, please do so first using the install.packages function.

require(tidyverse)
require(rstanarm)
require(magrittr)
require(rstan)
require(bayesplot)
require(loo)
require(readxl)

For this lab, you will need two stan files lab-03-poisson-simple.stan and lab-03-poisson-simple.stan, which you can download here:

Download both and make sure to save them in the same folder as the R script or R markdown file you are working from.

The Data

The data we have are counts of deaths per episode of Game of Thrones. Download the data (named GoT_Deaths.xlsx) from Sakai and save it locally to the same directory as your R markdown file. To find the data file on Sakai, go to Resources \(\rightarrow\) Datasets \(\rightarrow\) Lab Datasets \(\rightarrow\) Lab 3. Once you have downloaded the data file into the SAME folder as your R markdown file, load the data by using the following R code.

GoT <- read_xlsx("GoT_Deaths.xlsx", col_names = T)
head(GoT)
## # A tibble: 6 x 3
##   Season Episode Count
##    <dbl>   <dbl> <dbl>
## 1      1       1     4
## 2      1       2     3
## 3      1       3     0
## 4      1       4     1
## 5      1       5     5
## 6      1       6     4

  1. Plot a histogram of the death counts.

Because we have count data, it is natural to model the data with a Poisson distribution. If we take the empirical mean of the data as our estimate for \(\lambda\), what does the sampling distribution look like?

y <- GoT$Count
n <- length(y)

# Finish: obtain empirical mean
ybar <- mean(y)
sim_dat <- rpois(n, ybar)
qplot(sim_dat, bins = 20, xlab = "Simulated number of deaths", fill = I("#9ecae1"))

# create data frame for side-by-side histograms
df <- rbind(data.frame(y, "observed") %>% rename(count = 1, data = 2),
            data.frame(sim_dat, "simulated") %>% rename(count = 1, data = 2))
ggplot(df, aes(x = count, fill = data))+
  geom_histogram(position = "dodge", bins = 20) +
  scale_fill_brewer()  +
  labs(x = "Number of deaths", y = "Count")

Plotting the histogram of the data next to the histogram of the sampled data using \(\hat{\lambda} = \bar{y}\), we see that there are many more 0-valued observations in the observed data than there are in the simulated data. We might suspect that the Poisson model will not be a good fit for the data. For now, let’s proceed using the Poisson model and see how it behaves.

Poisson model

We have learned that the Gamma distribution is conjugate for Poisson data. Here, we have chosen the prior \(\lambda \sim Gamma(10,2)\) based on prior knowledge that Game of Thrones is a show filled with death. We run the model in Stan. We save the posterior sampled values of \(\lambda\) in the variable lambda_draws.

stan_dat <- list(y = y, N = n)
fit <- stan("lab-03-poisson-simple.stan", data = stan_dat, refresh = 0, chains = 2)
lambda_draws <- as.matrix(fit, pars = "lambda")

  1. Use the function mcmc_areas() to plot the smoothed posterior distribution for \(\lambda\) with a 90% Highest Posterior Density region. Changing the prob parameter in mcmc_areas() will change the amount of probability mass that is highlighted. The highlighted region will begin in regions of highest density, and will move towards regions of lower density as prob gets larger.
mcmc_areas(lambda_draws, prob = 0.9)
print(fit, pars = "lambda")

The line in the plot represents the posterior mean, and the shaded area represents 90% of the posterior density. How does the posterior mean for \(\lambda\) compare to the sample mean?


Graphical Posterior Predictive Checks (PPC)


  1. Generate posterior predictive samples using the posterior values of \(\lambda\) and store the result in a length(lambda_draws) by n matrix called y_rep.

We now step through some graphical posterior predictive checks. Here we plot the histogram of the observed counts against several of the posterior predictions. What do you notice?

ppc_hist(y, y_rep[1:8, ], binwidth = 1)

We can compare the density estimate of \(y\) to the density estimates for several (60) of the \(y_rep\)s. What do you notice here?

ppc_dens_overlay(y, y_rep[1:60, ])

In our first histogram of the data, we noticed the high number of 0 counts. Let us calculate the proportion of zeros in \(y\), and compare that to the proportion of zeros in all of the posterior predictive samples.

prop_zero <- function(x){
  mean(x == 0)
} 
prop_zero(y)
## [1] 0.16
ppc_stat(y, y_rep, stat = "prop_zero")
## `stat_bin()` using `bins = 30`. Pick better value with `binwidth`.

We can plot the means and variances for all of the simulated datasets, along with the observed statistics.

ppc_stat_2d(y, y_rep, stat = c("mean", "var"))

ppc_error_hist(y, y_rep[1:4, ], binwidth = 1) + xlim(-15, 15)
## Warning: Removed 8 rows containing missing values (geom_bar).


  1. Based on on these PPCs, does this model appear to be a good fit for the data?

Poisson Hurdle Model

How should we account for the high frequency of zeros? As it turns out, there is a lot of literature on how to work with this sort of data. We can fit a zero-inflated Poisson model, where the data is modeled as a mixture of a Poisson distribution with a point mass at zero. Here, we fit a hurdle model: \(y_i = 0\) with probability \(\theta\), and \(y_i > 0\) with probability \(1-\theta\). Conditional on having observed \(y_i\) nonzero, we model \(y_i\) with a Poisson distribution which is truncated from below with a lower bound of 1. For the truncated Poisson, we use the same \(Gamma(10,2)\) prior as in the simple Poisson model above.


  1. Using the code provided for the simple Poisson model, simulate draws from the posterior density of \(\lambda\) with the “Poisson Hurdle” model. The Stan file you’ll need to use is called poisson-hurdle.stan. Store the resulting object in a variable called fit2.

Here we compare the posterior densities of \(\lambda\) from the simple Poisson model and the Poisson hurdle model.

# Extract the sampled vlaues for lambda, and store them in a variable called lambda_draws2:
lambda_draws2 <- as.matrix(fit2, pars = "lambda")

# Compare
lambdas <- cbind(lambda_fit1 = lambda_draws[, 1],
                 lambda_fit2 = lambda_draws2[, 1])

# Shade 90% interval
mcmc_areas(lambdas, prob = 0.9) 

Obtaining posterior samples from the hurdle model is more complicated, so the Stan file includes code to draw from the posterior predictive distribution for you. We extract them here, and store the predictive samples in y_rep2.

y_rep2 <- as.matrix(fit2, pars = "y_rep")

  1. Use the code given above to produce the same PPC visualizations as before for the new results. Comment on how this second model compares to both the observed data and to the simple Poisson model.

Leave-one-out cross-validation

Here, we assess the predictive performance of both models with leave-one-out cross-validation (LOOCV). LOOCV holds out a single observation form the sample, fits the model on the remaining observations, uses the held out data point as validation, and calculates the prediction error. This process is repeated \(n\) times, such that each observation has been held out exactly once. We make use of the hand loo() function, and compare the two models:

log_lik1 <- extract_log_lik(fit, merge_chains = FALSE)
r_eff1 <- relative_eff(exp(log_lik1)) 
(loo1 <- loo(log_lik1, r_eff = r_eff1))
## 
## Computed from 2000 by 73 log-likelihood matrix
## 
##          Estimate   SE
## elpd_loo   -203.2 14.6
## p_loo         2.6  0.5
## looic       406.4 29.1
## ------
## Monte Carlo SE of elpd_loo is 0.1.
## 
## All Pareto k estimates are good (k < 0.5).
## See help('pareto-k-diagnostic') for details.
log_lik2 <- extract_log_lik(fit2, merge_chains = FALSE)
r_eff2 <- relative_eff(exp(log_lik2)) 
(loo2 <- loo(log_lik2, r_eff = r_eff2))
## 
## Computed from 2000 by 73 log-likelihood matrix
## 
##          Estimate   SE
## elpd_loo   -183.2 10.8
## p_loo         2.7  0.4
## looic       366.3 21.6
## ------
## Monte Carlo SE of elpd_loo is 0.0.
## 
## All Pareto k estimates are good (k < 0.5).
## See help('pareto-k-diagnostic') for details.
compare(loo1, loo2)
## Warning: 'compare' is deprecated.
## Use 'loo_compare' instead.
## See help("Deprecated")
## elpd_diff        se 
##      20.1       8.5

  1. Which model performs better in terms of prediction?

Wrapping up


Some final questions to consider:

  1. Why are PPCs important?
  2. Was the second model a good fit for the data? Why or why not?
  3. If someone reported a single LOOCV error to you, would that be useful? Why or why not?

Grading

10 points: 1 point for each exercise.

Acknowledgement

This lab was adapted from this tutorial by Jordan Bryan and Becky Tang.