Hierarchical partial pooling with tfprobability

Earlier than we bounce into the technicalities: This submit is, after all, devoted to McElreath who wrote one in every of most intriguing books on Bayesian (or ought to we simply say – scientific?) modeling we’re conscious of. Should you haven’t learn Statistical Rethinking, and are all in favour of modeling, you may positively wish to test it out. On this submit, we’re not going to attempt to re-tell the story: Our clear focus will, as an alternative, be an indication of tips on how to do MCMC with tfprobability.

Concretely, this submit has two components. The primary is a fast overview of tips on how to use tfd_joint_sequential_distribution to assemble a mannequin, after which pattern from it utilizing Hamiltonian Monte Carlo. This half may be consulted for fast code look-up, or as a frugal template of the entire course of.
The second half then walks via a multi-level mannequin in additional element, exhibiting tips on how to extract, post-process and visualize sampling in addition to diagnostic outputs.

Reedfrogs

The info comes with the rethinking package deal.

'knowledge.body':   48 obs. of  5 variables:
 $ density : int  10 10 10 10 10 10 10 10 10 10 ...
 $ pred    : Issue w/ 2 ranges "no","pred": 1 1 1 1 1 1 1 1 2 2 ...
 $ dimension    : Issue w/ 2 ranges "huge","small": 1 1 1 1 2 2 2 2 1 1 ...
 $ surv    : int  9 10 7 10 9 9 10 9 4 9 ...
 $ propsurv: num  0.9 1 0.7 1 0.9 0.9 1 0.9 0.4 0.9 ...

The duty is modeling survivor counts amongst tadpoles, the place tadpoles are held in tanks of various sizes (equivalently, completely different numbers of inhabitants). Every row within the dataset describes one tank, with its preliminary depend of inhabitants (density) and variety of survivors (surv).
Within the technical overview half, we construct a easy unpooled mannequin that describes each tank in isolation. Then, within the detailed walk-through, we’ll see tips on how to assemble a various intercepts mannequin that enables for data sharing between tanks.

Establishing fashions with tfd_joint_distribution_sequential

tfd_joint_distribution_sequential represents a mannequin as a listing of conditional distributions.
That is best to see on an actual instance, so we’ll bounce proper in, creating an unpooled mannequin of the tadpole knowledge.

That is the how the mannequin specification would look in Stan:

mannequin{
    vector[48] p;
    a ~ regular( 0 , 1.5 );
    for ( i in 1:48 ) {
        p[i] = a[tank[i]];
        p[i] = inv_logit(p[i]);
    }
    S ~ binomial( N , p );
}

And right here is tfd_joint_distribution_sequential:

library(tensorflow)

# ensure you have a minimum of model 0.7 of TensorFlow Chance 
# as of this writing, it's required of set up the grasp department:
# install_tensorflow(model = "nightly")
library(tfprobability)

n_tadpole_tanks <- nrow(d)
n_surviving <- d$surv
n_start <- d$density

m1 <- tfd_joint_distribution_sequential(
  checklist(
    # regular prior of per-tank logits
    tfd_multivariate_normal_diag(
      loc = rep(0, n_tadpole_tanks),
      scale_identity_multiplier = 1.5),
    # binomial distribution of survival counts
    perform(l)
      tfd_independent(
        tfd_binomial(total_count = n_start, logits = l),
        reinterpreted_batch_ndims = 1
      )
  )
)

The mannequin consists of two distributions: Prior means and variances for the 48 tadpole tanks are specified by tfd_multivariate_normal_diag; then tfd_binomial generates survival counts for every tank.
Observe how the primary distribution is unconditional, whereas the second depends upon the primary. Observe too how the second must be wrapped in tfd_independent to keep away from fallacious broadcasting. (That is a facet of tfd_joint_distribution_sequential utilization that deserves to be documented extra systematically, which is definitely going to occur. Simply suppose that this performance was added to TFP grasp solely three weeks in the past!)

As an apart, the mannequin specification right here finally ends up shorter than in Stan as tfd_binomial optionally takes logits as parameters.

As with each TFP distribution, you are able to do a fast performance verify by sampling from the mannequin:

# pattern a batch of two values 
# we get samples for each distribution within the mannequin
s <- m1 %>% tfd_sample(2)

[[1]]
Tensor("MultivariateNormalDiag/pattern/affine_linear_operator/ahead/add:0",
form=(2, 48), dtype=float32)

[[2]]
Tensor("IndependentJointDistributionSequential/pattern/Beta/pattern/Reshape:0",
form=(2, 48), dtype=float32)

and computing log chances:

# we should always get solely the general log likelihood of the mannequin
m1 %>% tfd_log_prob(s)

t[[1]]
Tensor("MultivariateNormalDiag/pattern/affine_linear_operator/ahead/add:0",
form=(2, 48), dtype=float32)

[[2]]
Tensor("IndependentJointDistributionSequential/pattern/Beta/pattern/Reshape:0",
form=(2, 48), dtype=float32)

Now, let’s see how we are able to pattern from this mannequin utilizing Hamiltonian Monte Carlo.

Operating Hamiltonian Monte Carlo in TFP

We outline a Hamiltonian Monte Carlo kernel with dynamic step dimension adaptation based mostly on a desired acceptance likelihood.

# variety of steps to run burnin
n_burnin <- 500

# optimization goal is the probability of the logits given the information
logprob <- perform(l)
  m1 %>% tfd_log_prob(checklist(l, n_surviving))

hmc <- mcmc_hamiltonian_monte_carlo(
  target_log_prob_fn = logprob,
  num_leapfrog_steps = 3,
  step_size = 0.1,
) %>%
  mcmc_simple_step_size_adaptation(
    target_accept_prob = 0.8,
    num_adaptation_steps = n_burnin
  )

We then run the sampler, passing in an preliminary state. If we wish to run (n) chains, that state must be of size (n), for each parameter within the mannequin (right here we’ve got only one).

The sampling perform, mcmc_sample_chain, could optionally be handed a trace_fn that tells TFP which sorts of meta data to save lots of. Right here we save acceptance ratios and step sizes.

# variety of steps after burnin
n_steps <- 500
# variety of chains
n_chain <- 4

# get beginning values for the parameters
# their form implicitly determines the variety of chains we'll run
# see current_state parameter handed to mcmc_sample_chain beneath
c(initial_logits, .) %<-% (m1 %>% tfd_sample(n_chain))

# inform TFP to maintain observe of acceptance ratio and step dimension
trace_fn <- perform(state, pkr) {
  checklist(pkr$inner_results$is_accepted,
       pkr$inner_results$accepted_results$step_size)
}

res <- hmc %>% mcmc_sample_chain(
  num_results = n_steps,
  num_burnin_steps = n_burnin,
  current_state = initial_logits,
  trace_fn = trace_fn
)

When sampling is completed, we are able to entry the samples as res$all_states:

mcmc_trace <- res$all_states
mcmc_trace

Tensor("mcmc_sample_chain/trace_scan/TensorArrayStack/TensorArrayGatherV3:0",
form=(500, 4, 48), dtype=float32)

That is the form of the samples for l, the 48 per-tank logits: 500 samples occasions 4 chains occasions 48 parameters.

From these samples, we are able to compute efficient pattern dimension and (rhat) (alias mcmc_potential_scale_reduction):

# Tensor("Imply:0", form=(48,), dtype=float32)
ess <- mcmc_effective_sample_size(mcmc_trace) %>% tf$reduce_mean(axis = 0L)

# Tensor("potential_scale_reduction/potential_scale_reduction_single_state/sub_1:0", form=(48,), dtype=float32)
rhat <- mcmc_potential_scale_reduction(mcmc_trace)

Whereas diagnostic data is obtainable in res$hint:

# Tensor("mcmc_sample_chain/trace_scan/TensorArrayStack_1/TensorArrayGatherV3:0",
# form=(500, 4), dtype=bool)
is_accepted <- res$hint[[1]] 

# Tensor("mcmc_sample_chain/trace_scan/TensorArrayStack_2/TensorArrayGatherV3:0",
# form=(500,), dtype=float32)
step_size <- res$hint[[2]] 

After this fast define, let’s transfer on to the subject promised within the title: multi-level modeling, or partial pooling. This time, we’ll additionally take a better take a look at sampling outcomes and diagnostic outputs.

Multi-level tadpoles

The multi-level mannequin – or various intercepts mannequin, on this case: we’ll get to various slopes in a later submit – provides a hyperprior to the mannequin. As an alternative of deciding on a imply and variance of the conventional prior the logits are drawn from, we let the mannequin study means and variances for particular person tanks.
These per-tank means, whereas being priors for the binomial logits, are assumed to be usually distributed, and are themselves regularized by a standard prior for the imply and an exponential prior for the variance.

For the Stan-savvy, right here is the Stan formulation of this mannequin.

mannequin{
    vector[48] p;
    sigma ~ exponential( 1 );
    a_bar ~ regular( 0 , 1.5 );
    a ~ regular( a_bar , sigma );
    for ( i in 1:48 ) {
        p[i] = a[tank[i]];
        p[i] = inv_logit(p[i]);
    }
    S ~ binomial( N , p );
}

m2 <- tfd_joint_distribution_sequential(
  checklist(
    # a_bar, the prior for the imply of the conventional distribution of per-tank logits
    tfd_normal(loc = 0, scale = 1.5),
    # sigma, the prior for the variance of the conventional distribution of per-tank logits
    tfd_exponential(charge = 1),
    # regular distribution of per-tank logits
    # parameters sigma and a_bar seek advice from the outputs of the above two distributions
    perform(sigma, a_bar) 
      tfd_sample_distribution(
        tfd_normal(loc = a_bar, scale = sigma),
        sample_shape = checklist(n_tadpole_tanks)
      ), 
    # binomial distribution of survival counts
    # parameter l refers back to the output of the conventional distribution instantly above
    perform(l)
      tfd_independent(
        tfd_binomial(total_count = n_start, logits = l),
        reinterpreted_batch_ndims = 1
      )
  )
)

Technically, dependencies in tfd_joint_distribution_sequential are outlined by way of spatial proximity within the checklist: Within the realized prior for the logits

perform(sigma, a_bar) 
      tfd_sample_distribution(
        tfd_normal(loc = a_bar, scale = sigma),
        sample_shape = checklist(n_tadpole_tanks)
      )

sigma refers back to the distribution instantly above, and a_bar to the one above that.

Analogously, within the distribution of survival counts

perform(l)
      tfd_independent(
        tfd_binomial(total_count = n_start, logits = l),
        reinterpreted_batch_ndims = 1
      )

l refers back to the distribution instantly previous its personal definition.

Once more, let’s pattern from this mannequin to see if shapes are right.

s <- m2 %>% tfd_sample(2)
s 

They’re.

[[1]]
Tensor("Regular/sample_1/Reshape:0", form=(2,), dtype=float32)

[[2]]
Tensor("Exponential/sample_1/Reshape:0", form=(2,), dtype=float32)

[[3]]
Tensor("SampleJointDistributionSequential/sample_1/Regular/pattern/Reshape:0",
form=(2, 48), dtype=float32)

[[4]]
Tensor("IndependentJointDistributionSequential/sample_1/Beta/pattern/Reshape:0",
form=(2, 48), dtype=float32)

And to ensure we get one general log_prob per batch:

Tensor("JointDistributionSequential/log_prob/add_3:0", form=(2,), dtype=float32)

Coaching this mannequin works like earlier than, besides that now the preliminary state contains three parameters, a_bar, sigma and l:

c(initial_a, initial_s, initial_logits, .) %<-% (m2 %>% tfd_sample(n_chain))

Right here is the sampling routine:

# the joint log likelihood now's based mostly on three parameters
logprob <- perform(a, s, l)
  m2 %>% tfd_log_prob(checklist(a, s, l, n_surviving))

hmc <- mcmc_hamiltonian_monte_carlo(
  target_log_prob_fn = logprob,
  num_leapfrog_steps = 3,
  # one step dimension for every parameter
  step_size = checklist(0.1, 0.1, 0.1),
) %>%
  mcmc_simple_step_size_adaptation(target_accept_prob = 0.8,
                                   num_adaptation_steps = n_burnin)

run_mcmc <- perform(kernel) {
  kernel %>% mcmc_sample_chain(
    num_results = n_steps,
    num_burnin_steps = n_burnin,
    current_state = checklist(initial_a, tf$ones_like(initial_s), initial_logits),
    trace_fn = trace_fn
  )
}

res <- hmc %>% run_mcmc()
 
mcmc_trace <- res$all_states

This time, mcmc_trace is a listing of three: We have now

[[1]]
Tensor("mcmc_sample_chain/trace_scan/TensorArrayStack/TensorArrayGatherV3:0",
form=(500, 4), dtype=float32)

[[2]]
Tensor("mcmc_sample_chain/trace_scan/TensorArrayStack_1/TensorArrayGatherV3:0",
form=(500, 4), dtype=float32)

[[3]]
Tensor("mcmc_sample_chain/trace_scan/TensorArrayStack_2/TensorArrayGatherV3:0",
form=(500, 4, 48), dtype=float32)

Now let’s create graph nodes for the outcomes and knowledge we’re all in favour of.

# as above, that is the uncooked end result
mcmc_trace_ <- res$all_states

# we carry out some reshaping operations immediately in tensorflow
all_samples_ <-
  tf$concat(
    checklist(
      mcmc_trace_[[1]] %>% tf$expand_dims(axis = -1L),
      mcmc_trace_[[2]]  %>% tf$expand_dims(axis = -1L),
      mcmc_trace_[[3]]
    ),
    axis = -1L
  ) %>%
  tf$reshape(checklist(2000L, 50L))

# diagnostics, additionally as above
is_accepted_ <- res$hint[[1]]
step_size_ <- res$hint[[2]]

# efficient pattern dimension
# once more we use tensorflow to get conveniently formed outputs
ess_ <- mcmc_effective_sample_size(mcmc_trace) 
ess_ <- tf$concat(
  checklist(
    ess_[[1]] %>% tf$expand_dims(axis = -1L),
    ess_[[2]]  %>% tf$expand_dims(axis = -1L),
    ess_[[3]]
  ),
  axis = -1L
) 

# rhat, conveniently post-processed
rhat_ <- mcmc_potential_scale_reduction(mcmc_trace)
rhat_ <- tf$concat(
  checklist(
    rhat_[[1]] %>% tf$expand_dims(axis = -1L),
    rhat_[[2]]  %>% tf$expand_dims(axis = -1L),
    rhat_[[3]]
  ),
  axis = -1L
) 

And we’re prepared to really run the chains.

# to this point, no sampling has been accomplished!
# the precise sampling occurs after we create a Session 
# and run the above-defined nodes
sess <- tf$Session()
eval <- perform(...) sess$run(checklist(...))

c(mcmc_trace, all_samples, is_accepted, step_size, ess, rhat) %<-%
  eval(mcmc_trace_, all_samples_, is_accepted_, step_size_, ess_, rhat_)

This time, let’s really examine these outcomes.

Multi-level tadpoles: Outcomes

First, how do the chains behave?

Hint plots

Extract the samples for a_bar and sigma, in addition to one of many realized priors for the logits:

Right here’s a hint plot for a_bar:

prep_tibble <- perform(samples) {
  as_tibble(samples, .name_repair = ~ c("chain_1", "chain_2", "chain_3", "chain_4")) %>% 
    add_column(pattern = 1:500) %>%
    collect(key = "chain", worth = "worth", -pattern)
}

plot_trace <- perform(samples, param_name) {
  prep_tibble(samples) %>% 
    ggplot(aes(x = pattern, y = worth, coloration = chain)) +
    geom_line() + 
    ggtitle(param_name)
}

plot_trace(a_bar, "a_bar")

And right here for sigma and a_1:

How concerning the posterior distributions of the parameters, before everything, the various intercepts a_1 … a_48?

Posterior distributions

plot_posterior <- perform(samples) {
  prep_tibble(samples) %>% 
    ggplot(aes(x = worth, coloration = chain)) +
    geom_density() +
    theme_classic() +
    theme(legend.place = "none",
          axis.title = element_blank(),
          axis.textual content = element_blank(),
          axis.ticks = element_blank())
    
}

plot_posteriors <- perform(sample_array, num_params) {
  plots <- purrr::map(1:num_params, ~ plot_posterior(sample_array[ , , .x] %>% as.matrix()))
  do.name(grid.organize, plots)
}

plot_posteriors(mcmc_trace[[3]], dim(mcmc_trace[[3]])[3])

Now let’s see the corresponding posterior means and highest posterior density intervals.
(The beneath code contains the hyperpriors in abstract as we’ll wish to show a whole summary-like output quickly.)

Posterior means and HPDIs

all_samples <- all_samples %>%
  as_tibble(.name_repair = ~ c("a_bar", "sigma", paste0("a_", 1:48))) 

means <- all_samples %>% 
  summarise_all(checklist (~ imply)) %>% 
  collect(key = "key", worth = "imply")

sds <- all_samples %>% 
  summarise_all(checklist (~ sd)) %>% 
  collect(key = "key", worth = "sd")

hpdis <-
  all_samples %>%
  summarise_all(checklist(~ checklist(hdi(.) %>% t() %>% as_tibble()))) %>% 
  unnest() 

hpdis_lower <- hpdis %>% choose(-comprises("higher")) %>%
  rename(lower0 = decrease) %>%
  collect(key = "key", worth = "decrease") %>% 
  organize(as.integer(str_sub(key, 6))) %>%
  mutate(key = c("a_bar", "sigma", paste0("a_", 1:48)))

hpdis_upper <- hpdis %>% choose(-comprises("decrease")) %>%
  rename(upper0 = higher) %>%
  collect(key = "key", worth = "higher") %>% 
  organize(as.integer(str_sub(key, 6))) %>%
  mutate(key = c("a_bar", "sigma", paste0("a_", 1:48)))

abstract <- means %>% 
  inner_join(sds, by = "key") %>% 
  inner_join(hpdis_lower, by = "key") %>%
  inner_join(hpdis_upper, by = "key")


abstract %>% 
  filter(!key %in% c("a_bar", "sigma")) %>%
  mutate(key_fct = issue(key, ranges = distinctive(key))) %>%
  ggplot(aes(x = key_fct, y = imply, ymin = decrease, ymax = higher)) +
   geom_pointrange() + 
   coord_flip() +  
   xlab("") + ylab("submit. imply and HPDI") +
   theme_minimal() 

Now for an equal to summary. We already computed means, customary deviations and the HPDI interval.
Let’s add n_eff, the efficient variety of samples, and rhat, the Gelman-Rubin statistic.

Complete abstract (a.ok.a. “summary”)

is_accepted <- is_accepted %>% as.integer() %>% imply()
step_size <- purrr::map(step_size, imply)

ess <- apply(ess, 2, imply)

summary_with_diag <- abstract %>% add_column(ess = ess, rhat = rhat)
summary_with_diag

# A tibble: 50 x 7
   key    imply    sd  decrease higher   ess  rhat
   <chr> <dbl> <dbl>  <dbl> <dbl> <dbl> <dbl>
 1 a_bar  1.35 0.266  0.792  1.87 405.   1.00
 2 sigma  1.64 0.218  1.23   2.05  83.6  1.00
 3 a_1    2.14 0.887  0.451  3.92  33.5  1.04
 4 a_2    3.16 1.13   1.09   5.48  23.7  1.03
 5 a_3    1.01 0.698 -0.333  2.31  65.2  1.02
 6 a_4    3.02 1.04   1.06   5.05  31.1  1.03
 7 a_5    2.11 0.843  0.625  3.88  49.0  1.05
 8 a_6    2.06 0.904  0.496  3.87  39.8  1.03
 9 a_7    3.20 1.27   1.11   6.12  14.2  1.02
10 a_8    2.21 0.894  0.623  4.18  44.7  1.04
# ... with 40 extra rows

For the various intercepts, efficient pattern sizes are fairly low, indicating we would wish to examine potential causes.

Let’s additionally show posterior survival chances, analogously to determine 13.2 within the e book.

Posterior survival chances

sim_tanks <- rnorm(8000, a_bar, sigma)
tibble(x = sim_tanks) %>% ggplot(aes(x = x)) + geom_density() + xlab("distribution of per-tank logits")

# our standard sigmoid by one other title (undo the logit)
logistic <- perform(x) 1/(1 + exp(-x))
probs <- map_dbl(sim_tanks, logistic)
tibble(x = probs) %>% ggplot(aes(x = x)) + geom_density() + xlab("likelihood of survival")

Lastly, we wish to be certain that we see the shrinkage conduct displayed in determine 13.1 within the e book.

Shrinkage

abstract %>% 
  filter(!key %in% c("a_bar", "sigma")) %>%
  choose(key, imply) %>%
  mutate(est_survival = logistic(imply)) %>%
  add_column(act_survival = d$propsurv) %>%
  choose(-imply) %>%
  collect(key = "kind", worth = "worth", -key) %>%
  ggplot(aes(x = key, y = worth, coloration = kind)) +
  geom_point() +
  geom_hline(yintercept = imply(d$propsurv), dimension = 0.5, coloration = "cyan" ) +
  xlab("") +
  ylab("") +
  theme_minimal() +
  theme(axis.textual content.x = element_blank())

We see outcomes comparable in spirit to McElreath’s: estimates are shrunken to the imply (the cyan-colored line). Additionally, shrinkage appears to be extra energetic in smaller tanks, that are the lower-numbered ones on the left of the plot.

Outlook

On this submit, we noticed tips on how to assemble a various intercepts mannequin with tfprobability, in addition to tips on how to extract sampling outcomes and related diagnostics. In an upcoming submit, we’ll transfer on to various slopes.
With non-negligible likelihood, our instance will construct on one in every of Mc Elreath’s once more…
Thanks for studying!