**BioStatMatt » R**, and kindly contributed to R-bloggers)

I recently decided to revisit some `R` code that implements a Gibbs sampler in an attempt to decrease the iteration time. My strategy was to implement the sampler state as an `R` environment rather than a list. The rationale was that passing an environment to and from functions would reduce the amount of duplication (memory copying). In my experiments, this results in only marginal improvement in iteration time. The following is just a toy example to illustrate.

Consider the logistic regression model

where is a binary outcome, independently Bernoulli distributed with probability , is a scalar covariate, and the log odds is

*a priori*normal distributed with mean and precision .

For Gibbs sampling, it’s convenient to store and manupulate a model *state*. In the past, I had represented this in `R` with a list, for example

> logit <- function(e) log(e) - log(1-e) > expit <- function(l) exp(l) / (1+exp(l)) > # Simulate some data > n <- 1e3 > x <- runif(n) > y <- rbinom(n, 1, expit(5*x)) > iter <- 0 > itermax <- 1000 > state <- list(x=x, y=y, mu=0, tau=1e-3, beta=rep(0,itermax), iter=1)

Then, to perform a Gibbs update on beta, I would pass the old state to a function that would return the updated state. For example:

> Gibbs <- function(state) { + # Metropolis update + state$iter <- state$iter + 1 + + old_beta <- state$beta[state$iter-1] + old_probs <- expit(old_beta*state$x) + old_logp <- sum(log(ifelse(state$y,old_probs,1-old_probs))) + + dnorm(old_beta, state$mu, 1/sqrt(state$tau), log=TRUE) + + new_beta <- rnorm(1, old_beta) # Proposal + new_probs <- expit(new_beta*state$x) + new_logp <- sum(log(ifelse(state$y,new_probs,1-new_probs))) + + dnorm(new_beta, state$mu, 1/sqrt(state$tau), log=TRUE) + + if(new_logp - old_logp > log(runif(1))) + state$beta[state$iter] <- new_beta + else + state$beta[state$iter] <- old_beta + + return(state) + }

Hence, the Gibbs sampler would be used as follows

> system.time({ + while(state$iter < itermax) + state <- Gibbs(state) + }) user system elapsed 2.708 0.012 2.717 > summary(state$beta) Min. 1st Qu. Median Mean 3rd Qu. Max. 0.000 4.414 4.564 4.515 4.792 5.417

Alternatively, the Gibbs sampler state may be stored and manipulated asan `R` environment. For example, to initialize the state:

> estate <- new.env() > assign("x", x, envir=estate) > assign("y", y, envir=estate) > assign("mu", 0, envir=estate) > assign("tau", 1e-3, envir=estate) > assign("beta", rep(0,itermax), envir=estate) > assign("iter", 1, envir=estate)

Then rewrite the Gibbs sampler function:

> GibbsExp <- expression({ + # Metropolis update + iter <- iter + 1 + + old_beta <- beta[iter-1] + old_probs <- expit(old_beta*x) + old_logp <- sum(log(ifelse(y,old_probs,1-old_probs))) + + dnorm(old_beta, mu, 1/sqrt(tau), log=TRUE) + + new_beta <- rnorm(1, old_beta) # Proposal + new_probs <- expit(new_beta*x) + new_logp <- sum(log(ifelse(y,new_probs,1-new_probs))) + + dnorm(new_beta, mu, 1/sqrt(tau), log=TRUE) + + if(new_logp - old_logp > log(runif(1))) + beta[iter] <- new_beta + else + beta[iter] <- old_beta + }) > > eGibbs <- function(estate) { + eval(GibbsExp, estate) + }

The Gibbs sampler is used in an almost identical manner:

> system.time({ + while(get("iter",envir=estate) < itermax) + eGibbs(estate) + }) user system elapsed 2.664 0.000 2.673 > summary(get("beta",envir=estate)) Min. 1st Qu. Median Mean 3rd Qu. Max. 0.000 4.378 4.588 4.556 4.779 5.704

The percent decrease in iteration time is fairly constant for a variety of `n` and `maxiter` values. Presumably, this modest gain in speed results from less memory duplication. However, in some experiments with `tracemem` the story appears to be more complicated… For now, it doesn’t appear that utilizing environments is worth the trouble when the sampling algorithm is much slower than memory allocation.

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**BioStatMatt » R**.

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