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Bayesian Poisson Regression

This notebook is ported from the example notebook of PyMC3 on Poisson Regression.

Poisson Regression is a technique commonly used to model count data. Some of the applications include predicting the number of people defaulting on their loans or the number of cars running on a highway on a given day. This example describes a method to implement the Bayesian version of this technique using Turing.

We will generate the dataset that we will be working on which describes the relationship between number of times a person sneezes during the day with his alcohol consumption and medicinal intake.

We start by importing the required libraries.

#Import Turing, Distributions and DataFrames
using Turing, Distributions, DataFrames, Distributed

# Import MCMCChain, Plots, and StatsPlots for visualizations and diagnostics.
using MCMCChains, Plots, StatsPlots

# Set a seed for reproducibility.
using Random

# Turn off progress monitor.

Generating data

We start off by creating a toy dataset. We take the case of a person who takes medicine to prevent excessive sneezing. Alcohol consumption increases the rate of sneezing for that person. Thus, the two factors affecting the number of sneezes in a given day are alcohol consumption and whether the person has taken his medicine. Both these variable are taken as boolean valued while the number of sneezes will be a count valued variable. We also take into consideration that the interaction between the two boolean variables will affect the number of sneezes

5 random rows are printed from the generated data to get a gist of the data generated.

theta_noalcohol_meds = 1    # no alcohol, took medicine
theta_alcohol_meds = 3      # alcohol, took medicine
theta_noalcohol_nomeds = 6  # no alcohol, no medicine
theta_alcohol_nomeds = 36   # alcohol, no medicine

# no of samples for each of the above cases
q = 100

#Generate data from different Poisson distributions
noalcohol_meds = Poisson(theta_noalcohol_meds)
alcohol_meds = Poisson(theta_alcohol_meds)
noalcohol_nomeds = Poisson(theta_noalcohol_nomeds)
alcohol_nomeds = Poisson(theta_alcohol_nomeds)

nsneeze_data = vcat(
    rand(noalcohol_meds, q),
    rand(alcohol_meds, q),
    rand(noalcohol_nomeds, q),
    rand(alcohol_nomeds, q),
alcohol_data = vcat(zeros(q), ones(q), zeros(q), ones(q))
meds_data = vcat(zeros(q), zeros(q), ones(q), ones(q))

df = DataFrame(;
    product_alcohol_meds=meds_data .* alcohol_data,
df[sample(1:nrow(df), 5; replace=false), :]
5×4 DataFrame
 Row │ nsneeze  alcohol_taken  nomeds_taken  product_alcohol_meds
     │ Int64    Float64        Float64       Float64
   1 │       3            1.0           0.0                   0.0
   2 │       3            0.0           0.0                   0.0
   3 │       7            0.0           1.0                   0.0
   4 │       3            1.0           0.0                   0.0
   5 │       2            0.0           0.0                   0.0

Visualisation of the dataset

We plot the distribution of the number of sneezes for the 4 different cases taken above. As expected, the person sneezes the most when he has taken alcohol and not taken his medicine. He sneezes the least when he doesn't consume alcohol and takes his medicine.

#Data Plotting

p1 = Plots.histogram(
    df[(df[:, :alcohol_taken] .== 0) .& (df[:, :nomeds_taken] .== 0), 1];
p2 = Plots.histogram(
    (df[(df[:, :alcohol_taken] .== 1) .& (df[:, :nomeds_taken] .== 0), 1]);
p3 = Plots.histogram(
    (df[(df[:, :alcohol_taken] .== 0) .& (df[:, :nomeds_taken] .== 1), 1]);
p4 = Plots.histogram(
    (df[(df[:, :alcohol_taken] .== 1) .& (df[:, :nomeds_taken] .== 1), 1]);
plot(p1, p2, p3, p4; layout=(2, 2), legend=false)

We must convert our DataFrame data into the Matrix form as the manipulations that we are about are designed to work with Matrix data. We also separate the features from the labels which will be later used by the Turing sampler to generate samples from the posterior.

# Convert the DataFrame object to matrices.
data = Matrix(df[:, [:alcohol_taken, :nomeds_taken, :product_alcohol_meds]])
data_labels = df[:, :nsneeze]
400×3 Matrix{Float64}:
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 0.0  0.0  0.0
 1.0  1.0  1.0
 1.0  1.0  1.0
 1.0  1.0  1.0
 1.0  1.0  1.0
 1.0  1.0  1.0
 1.0  1.0  1.0
 1.0  1.0  1.0
 1.0  1.0  1.0
 1.0  1.0  1.0

We must recenter our data about 0 to help the Turing sampler in initialising the parameter estimates. So, normalising the data in each column by subtracting the mean and dividing by the standard deviation:

# # Rescale our matrices.
data = (data .- mean(data; dims=1)) ./ std(data; dims=1)
400×3 Matrix{Float64}:
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
 -0.998749  -0.998749  -0.576628
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988
  0.998749   0.998749   1.72988

Declaring the Model: Poisson Regression

Our model, poisson_regression takes four arguments:

  • x is our set of independent variables;
  • y is the element we want to predict;
  • n is the number of observations we have; and
  • σ² is the standard deviation we want to assume for our priors.

Within the model, we create four coefficients (b0, b1, b2, and b3) and assign a prior of normally distributed with means of zero and standard deviations of σ². We want to find values of these four coefficients to predict any given y.

Intuitively, we can think of the coefficients as:

  • b1 is the coefficient which represents the effect of taking alcohol on the number of sneezes;
  • b2 is the coefficient which represents the effect of taking in no medicines on the number of sneezes;
  • b3 is the coefficient which represents the effect of interaction between taking alcohol and no medicine on the number of sneezes;

The for block creates a variable theta which is the weighted combination of the input features. We have defined the priors on these weights above. We then observe the likelihood of calculating theta given the actual label, y[i].

# Bayesian poisson regression (LR)
@model function poisson_regression(x, y, n, σ²)
    b0 ~ Normal(0, σ²)
    b1 ~ Normal(0, σ²)
    b2 ~ Normal(0, σ²)
    b3 ~ Normal(0, σ²)
    for i in 1:n
        theta = b0 + b1 * x[i, 1] + b2 * x[i, 2] + b3 * x[i, 3]
        y[i] ~ Poisson(exp(theta))

Sampling from the posterior

We use the NUTS sampler to sample values from the posterior. We run multiple chains using the MCMCThreads() function to nullify the effect of a problematic chain. We then use the Gelman, Rubin, and Brooks Diagnostic to check the convergence of these multiple chains.

# Retrieve the number of observations.
n, _ = size(data)

# Sample using NUTS.

num_chains = 4
m = poisson_regression(data, data_labels, n, 10)
chain = sample(m, NUTS(200, 0.65), MCMCThreads(), 2_500, num_chains; discard_adapt=false)
Chains MCMC chain (2500×16×4 Array{Float64, 3}):

Iterations        = 1:1:2500
Number of chains  = 4
Samples per chain = 2500
Wall duration     = 12.5 seconds
Compute duration  = 12.04 seconds
parameters        = b2, b1, b3, b0
internals         = lp, n_steps, is_accept, acceptance_rate, log_density, h
amiltonian_energy, hamiltonian_energy_error, max_hamiltonian_energy_error, 
tree_depth, numerical_error, step_size, nom_step_size

Summary Statistics
  parameters      mean       std   naive_se      mcse        ess      rhat 
  e ⋯
      Symbol   Float64   Float64    Float64   Float64    Float64   Float64 

          b0    1.6313    0.1518     0.0015    0.0088   235.7648    1.0115 
          b1    0.5496    0.0925     0.0009    0.0052   242.8889    1.0150 
          b2    0.8848    0.1099     0.0011    0.0075   162.1375    1.0208 
          b3    0.2969    0.1033     0.0010    0.0050   396.4411    1.0120 
                                                                1 column om

  parameters      2.5%     25.0%     50.0%     75.0%     97.5%
      Symbol   Float64   Float64   Float64   Float64   Float64

          b0    1.5770    1.6223    1.6430    1.6635    1.7028
          b1    0.4364    0.5111    0.5491    0.5869    0.6730
          b2    0.7732    0.8429    0.8783    0.9144    0.9950
          b3    0.1831    0.2587    0.2934    0.3300    0.4003

Viewing the Diagnostics

We use the Gelman, Rubin, and Brooks Diagnostic to check whether our chains have converged. Note that we require multiple chains to use this diagnostic which analyses the difference between these multiple chains.

We expect the chains to have converged. This is because we have taken sufficient number of iterations (1500) for the NUTS sampler. However, in case the test fails, then we will have to take a larger number of iterations, resulting in longer computation time.

Gelman, Rubin, and Brooks Diagnostic
  parameters      psrf     97.5%
      Symbol   Float64   Float64

          b0    1.1787    1.2356
          b1    1.0343    1.0574
          b2    1.1943    1.3218
          b3    1.0813    1.1067

From the above diagnostic, we can conclude that the chains have converged because the PSRF values of the coefficients are close to 1.

So, we have obtained the posterior distributions of the parameters. We transform the coefficients and recover theta values by taking the exponent of the meaned values of the coefficients b0, b1, b2 and b3. We take the exponent of the means to get a better comparison of the relative values of the coefficients. We then compare this with the intuitive meaning that was described earlier.

# Taking the first chain
c1 = chain[:, :, 1]

# Calculating the exponentiated means
b0_exp = exp(mean(c1[:b0]))
b1_exp = exp(mean(c1[:b1]))
b2_exp = exp(mean(c1[:b2]))
b3_exp = exp(mean(c1[:b3]))

print("The exponent of the meaned values of the weights (or coefficients are): \n")
println("b0: ", b0_exp)
println("b1: ", b1_exp)
println("b2: ", b2_exp)
println("b3: ", b3_exp)
print("The posterior distributions obtained after sampling can be visualised as :\n")
The exponent of the meaned values of the weights (or coefficients are): 
b0: 5.162963380481074
b1: 1.729974010078183
b2: 2.408331691827242
b3: 1.343819380971721
The posterior distributions obtained after sampling can be visualised as :

Visualising the posterior by plotting it:


Interpreting the Obtained Mean Values

The exponentiated mean of the coefficient b1 is roughly half of that of b2. This makes sense because in the data that we generated, the number of sneezes was more sensitive to the medicinal intake as compared to the alcohol consumption. We also get a weaker dependence on the interaction between the alcohol consumption and the medicinal intake as can be seen from the value of b3.

Removing the Warmup Samples

As can be seen from the plots above, the parameters converge to their final distributions after a few iterations. These initial values during the warmup phase increase the standard deviations of the parameters and are not required after we get the desired distributions. Thus, we remove these warmup values and once again view the diagnostics.

To remove these warmup values, we take all values except the first 200. This is because we set the second parameter of the NUTS sampler (which is the number of adaptations) to be equal to 200. describe(chain) is used to view the standard deviations in the estimates of the parameters. It also gives other useful information such as the means and the quantiles.

# Note the standard deviation before removing the warmup samples
2-element Vector{MCMCChains.ChainDataFrame}:
 Summary Statistics (4 x 8)
 Quantiles (4 x 6)
# Removing the first 200 values of the chains.
chains_new = chain[201:2500, :, :]
2-element Vector{MCMCChains.ChainDataFrame}:
 Summary Statistics (4 x 8)
 Quantiles (4 x 6)

As can be seen from the numeric values and the plots above, the standard deviation values have decreased and all the plotted values are from the estimated posteriors. The exponentiated mean values, with the warmup samples removed, have not changed by much and they are still in accordance with their intuitive meanings as described earlier.


These tutorials are a part of the TuringTutorials repository, found at:

To locally run this tutorial, do the following commands:

using TuringTutorials
TuringTutorials.weave("07-poisson-regression", "07_poisson-regression.jmd")

Computer Information:

Julia Version 1.6.6
Commit b8708f954a (2022-03-28 07:17 UTC)
Platform Info:
  OS: Linux (x86_64-pc-linux-gnu)
  CPU: AMD EPYC 7502 32-Core Processor
  LIBM: libopenlibm
  LLVM: libLLVM-11.0.1 (ORCJIT, znver2)
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  JULIA_DEPOT_PATH = /cache/julia-buildkite-plugin/depots/7aa0085e-79a4-45f3-a5bd-9743c91cf3da

Package Information:

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  [78b55507] Gettext_jll v0.21.0+0
  [7746bdde] Glib_jll v2.68.3+2
  [3b182d85] Graphite2_jll v1.3.14+0
  [2e76f6c2] HarfBuzz_jll v2.8.1+1
  [1d5cc7b8] IntelOpenMP_jll v2018.0.3+2
  [aacddb02] JpegTurbo_jll v2.1.2+0
  [c1c5ebd0] LAME_jll v3.100.1+0
  [dd4b983a] LZO_jll v2.10.1+0
  [e9f186c6] Libffi_jll v3.2.2+1
  [d4300ac3] Libgcrypt_jll v1.8.7+0
  [7e76a0d4] Libglvnd_jll v1.3.0+3
  [7add5ba3] Libgpg_error_jll v1.42.0+0
  [94ce4f54] Libiconv_jll v1.16.1+1
  [4b2f31a3] Libmount_jll v2.35.0+0
  [3ae2931a] Libtask_jll v0.4.3+0
  [89763e89] Libtiff_jll v4.3.0+0
  [38a345b3] Libuuid_jll v2.36.0+0
  [856f044c] MKL_jll v2021.1.1+2
  [e7412a2a] Ogg_jll v1.3.5+1
  [458c3c95] OpenSSL_jll v1.1.13+0
  [efe28fd5] OpenSpecFun_jll v0.5.5+0
  [91d4177d] Opus_jll v1.3.2+0
  [2f80f16e] PCRE_jll v8.44.0+0
  [30392449] Pixman_jll v0.40.1+0
  [ea2cea3b] Qt5Base_jll v5.15.3+0
  [f50d1b31] Rmath_jll v0.3.0+0
  [a2964d1f] Wayland_jll v1.19.0+0
  [2381bf8a] Wayland_protocols_jll v1.23.0+0
  [02c8fc9c] XML2_jll v2.9.12+0
  [aed1982a] XSLT_jll v1.1.34+0
  [4f6342f7] Xorg_libX11_jll v1.6.9+4
  [0c0b7dd1] Xorg_libXau_jll v1.0.9+4
  [935fb764] Xorg_libXcursor_jll v1.2.0+4
  [a3789734] Xorg_libXdmcp_jll v1.1.3+4
  [1082639a] Xorg_libXext_jll v1.3.4+4
  [d091e8ba] Xorg_libXfixes_jll v5.0.3+4
  [a51aa0fd] Xorg_libXi_jll v1.7.10+4
  [d1454406] Xorg_libXinerama_jll v1.1.4+4
  [ec84b674] Xorg_libXrandr_jll v1.5.2+4
  [ea2f1a96] Xorg_libXrender_jll v0.9.10+4
  [14d82f49] Xorg_libpthread_stubs_jll v0.1.0+3
  [c7cfdc94] Xorg_libxcb_jll v1.13.0+3
  [cc61e674] Xorg_libxkbfile_jll v1.1.0+4
  [12413925] Xorg_xcb_util_image_jll v0.4.0+1
  [2def613f] Xorg_xcb_util_jll v0.4.0+1
  [975044d2] Xorg_xcb_util_keysyms_jll v0.4.0+1
  [0d47668e] Xorg_xcb_util_renderutil_jll v0.3.9+1
  [c22f9ab0] Xorg_xcb_util_wm_jll v0.4.1+1
  [35661453] Xorg_xkbcomp_jll v1.4.2+4
  [33bec58e] Xorg_xkeyboard_config_jll v2.27.0+4
  [c5fb5394] Xorg_xtrans_jll v1.4.0+3
  [3161d3a3] Zstd_jll v1.5.2+0
  [0ac62f75] libass_jll v0.15.1+0
  [f638f0a6] libfdk_aac_jll v2.0.2+0
  [b53b4c65] libpng_jll v1.6.38+0
  [f27f6e37] libvorbis_jll v1.3.7+1
  [1270edf5] x264_jll v2021.5.5+0
  [dfaa095f] x265_jll v3.5.0+0
  [d8fb68d0] xkbcommon_jll v0.9.1+5
  [0dad84c5] ArgTools
  [56f22d72] Artifacts
  [2a0f44e3] Base64
  [ade2ca70] Dates
  [8bb1440f] DelimitedFiles
  [8ba89e20] Distributed
  [f43a241f] Downloads
  [9fa8497b] Future
  [b77e0a4c] InteractiveUtils
  [4af54fe1] LazyArtifacts
  [b27032c2] LibCURL
  [76f85450] LibGit2
  [8f399da3] Libdl
  [37e2e46d] LinearAlgebra
  [56ddb016] Logging
  [d6f4376e] Markdown
  [a63ad114] Mmap
  [ca575930] NetworkOptions
  [44cfe95a] Pkg
  [de0858da] Printf
  [3fa0cd96] REPL
  [9a3f8284] Random
  [ea8e919c] SHA
  [9e88b42a] Serialization
  [1a1011a3] SharedArrays
  [6462fe0b] Sockets
  [2f01184e] SparseArrays
  [10745b16] Statistics
  [4607b0f0] SuiteSparse
  [fa267f1f] TOML
  [a4e569a6] Tar
  [8dfed614] Test
  [cf7118a7] UUIDs
  [4ec0a83e] Unicode
  [e66e0078] CompilerSupportLibraries_jll
  [deac9b47] LibCURL_jll
  [29816b5a] LibSSH2_jll
  [c8ffd9c3] MbedTLS_jll
  [14a3606d] MozillaCACerts_jll
  [4536629a] OpenBLAS_jll
  [05823500] OpenLibm_jll
  [83775a58] Zlib_jll
  [8e850ede] nghttp2_jll
  [3f19e933] p7zip_jll