knitr::opts_chunk$set(fig.width=8.5, fig.height=5.5, fig.align='center', warning=FALSE, message=FALSE)
library(DHARMa) set.seed(123)
In principle, DHARMa residuals can be calculated and interpreted for Bayesian models in very much the same way as for frequentist models. Therefore, all comments regarding tests, residual interpretation etc. from the main vignette are equally valid for Bayesian model checks. There are some minor differences regarding the expected null distribution of the residuals, in particular in the low data limit, but I believe that for most people, these are of less concern.
The main difference for a Bayesian user is that, unlike for users of directly supported regression packages such as lme4 or glmmTMB, most Bayesian users will have to create the simulations for the fitted model themselves and then feed them into DHARMa by hand. The basic workflow for Bayesians that work with BUGS, JAGS, STAN or similar is:
This is more easy as it sounds. For the major Bayesian samplers (e.g. BUGS, JAGS, STAN), it amounts to adding a block with data simulations to the model, and observing those during the MCMC sampling. Then, feed the simulations into DHARMa via createDHARMa, and all else will work pretty much the same as in the main vignette.
Here is an example, with JAGS
library(rjags) library(BayesianTools) set.seed(123) dat <- DHARMa::createData(200, overdispersion = 0.2) Data = as.list(dat) Data$nobs = nrow(dat) Data$nGroups = length(unique(dat$group)) modelCode = "model{ for(i in 1:nobs){ observedResponse[i] ~ dpois(lambda[i]) # poisson error distribution lambda[i] <- exp(eta[i]) # inverse link function eta[i] <- intercept + env*Environment1[i] # linear predictor } intercept ~ dnorm(0,0.0001) env ~ dnorm(0,0.0001) # Posterior predictive simulations for (i in 1:nobs) { observedResponseSim[i]~dpois(lambda[i]) } }" jagsModel <- jags.model(file= textConnection(modelCode), data=Data, n.chains = 3) para.names <- c("intercept","env", "lambda", "observedResponseSim") Samples <- coda.samples(jagsModel, variable.names = para.names, n.iter = 5000) x = BayesianTools::getSample(Samples) colnames(x) # problem: all the variables are in one array - this is better in STAN, where this is a list - have to extract the right columns by hand posteriorPredDistr = x[,3:202] # this is the uncertainty of the mean prediction (lambda) posteriorPredSim = x[,203:402] # these are the simulations sim = createDHARMa(simulatedResponse = t(posteriorPredSim), observedResponse = dat$observedResponse, fittedPredictedResponse = apply(posteriorPredDistr, 2, median), integerResponse = T) plot(sim)
In the created plots, you will see overdispersion, which is completely expected, as the simulated data has overdispersion and a RE, which is not accounted for by the Jags model.
As an exercise, you could now:
And check how the residuals improve.
The most important consideration in using DHARMa with Bayesian models is how to create the simulations. You can see in my jags code that the block
# Posterior predictive simulations for (i in 1:nobs) { observedResponseSim[i]~dpois(lambda[i]) }
performs the posterior predictive simulations. Here, we just take the predicted lambda (mean perdictions) during the MCMC simulations and sample from the assumed distribution. This will works for any non-hierarchical model.
When we move to hierarchical or multi-level models, including GLMMs, the issue of simulation becomes a bit more complicated. In a hierarchical model, there are several random processes that sit on top of each other. In the same way as explained in the main vignette at the point conditional / unconditional simulations, we will have to decide which of these random processes should be included in the posterior predictive simulations.
As an example, imagine we add a RE in the likelihood of the previous model, to account for the group structure in the data.
for(i in 1:nobs){ observedResponse[i] ~ dpois(lambda[i]) # poisson error distribution lambda[i] <- exp(eta[i]) # inverse link function eta[i] <- intercept + env*Environment1[i] + RE[group[i]] # linear predictor } for(j in 1:nGroups){ RE[j] ~ dnorm(0,tauRE) }
The predictions lambda[i] now depend on a lower-level stochastic effect, which is described by RE[j] ~ dnorm(0,tauRE). We can now decide to create posterior predictive simulations conditional on posterior estimates RE[j] (conditional simulations), in which case we would have to change nothing in the block for the posterior predictive simulations. Alternatively, we can decide that we want to re-simulate the RE (unconditional simulations), in which case we have to copy the entire structure of the likelihood in the predictions
for(j in 1:nGroups){ RESim[j] ~ dnorm(0,tauRE) } for (i in 1:nobs) { observedResponseSim[i] ~ dpois(lambdaSim[i]) lambdaSim[i] <- exp(etaSim[i]) etaSim[i] <- intercept + env*Environment1[i] + RESim[group[i]] }
Essentially, you can remember that if you want full (uncoditional) simulations, you basically have to copy the entire likelihood of the hierarchical model, minus the priors, and sample along the hierarchical model structure. If you want to condition on a part of this structure, just cut the DAG at the point on which you want to condition on.
A common question is if there are differences between Bayesian and MLE quantile residuals.
First of all, note that MLE and Bayesian quantile residuals are not exactly identical. The main difference is in how the simulation of the data under the fitted model are performed:
For models fitted by MLE, simulations in DHARMa are with the MLE (point estimate)
For models fitted with Bayes, simulations are practically always performed while also drawing from the posterior parameter uncertainty (as a point estimate is not available).
Thus, Bayesian posterior predictive simulations include the parametric uncertainty of the model, additionally to the sampling uncertainty. From this we can directly conclude that Bayesian and MLE quantile residuals are asymptotically identical (and via the usual arguments uniformly distributed), but become more different the smaller n becomes.
To examine what those differences are, let's imagine that we start with a situation of infinite data. In this case, we have a "sharp" posterior that can be viewed as identical to the MLE.
If we reduce the number of data, there are two things happening
The posterior gets wider, with the likelihood component being normally distributed, at least initially
The influence of the prior increases, the faster the stronger the prior is.
Thus, if we reduce the data, for weak / uninformative priors, we will simulate data while sampling parameters from a normal distribution around the MLE, while for strong priors, we will effectively sample data while drawing parameters of the model from the prior.
In particular in the latter case (prior dominates, which can be checked via prior sensitivity analysis), you may see residual patterns that are caused by the prior, even though the model structure is correct. In some sense, you could say that the residuals check if the combination of prior + structure is compatible with the data. It's a philosophical debate how to react on such a deviation, as the prior is not really negotiable in a Bayesian analysis.
Of course, also the MLE distribution might get problems in low data situations, but I would argue that MLE is usually only used anyway if the MLE is reasonably sharp. In practice, I have self experienced problems with MLE estimates. It's a bit different in the Bayesian case, where it is possible and often done to fit very complex models with limited data. In this case, many of the general issues in defining null distributions for Bayesian p-values (as, e.g., reviewed in Conn et al., 2018) apply.
I would add though that while I find it important that users are aware of those differences, I have found that in practice these issues are small, and usually overruled by the much stronger effects of model error.
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