Efficient approximate leave-one-out cross-validation (LOO) using subsampling
Source:R/loo_subsample.R
loo_subsample.brmsfit.RdEfficient approximate leave-one-out cross-validation (LOO) using subsampling
Usage
# S3 method for class 'brmsfit'
loo_subsample(x, ..., compare = TRUE, resp = NULL, model_names = NULL)Arguments
- x
A
brmsfitobject.- ...
More
brmsfitobjects or further arguments passed to the underlying post-processing functions. In particular, seeprepare_predictionsfor further supported arguments.- compare
A flag indicating if the information criteria of the models should be compared to each other via
loo_compare.- resp
Optional names of response variables. If specified, predictions are performed only for the specified response variables.
- model_names
If
NULL(the default) will use model names derived from deparsing the call. Otherwise will use the passed values as model names.
Details
More details can be found on
loo_subsample.
Examples
# \dontrun{
# model with population-level effects only
fit1 <- brm(rating ~ treat + period + carry,
data = inhaler)
#> Compiling Stan program...
#> Start sampling
#>
#> SAMPLING FOR MODEL 'anon_model' NOW (CHAIN 1).
#> Chain 1:
#> Chain 1: Gradient evaluation took 1.4e-05 seconds
#> Chain 1: 1000 transitions using 10 leapfrog steps per transition would take 0.14 seconds.
#> Chain 1: Adjust your expectations accordingly!
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#> SAMPLING FOR MODEL 'anon_model' NOW (CHAIN 2).
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#> Chain 2: Gradient evaluation took 6e-06 seconds
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#> SAMPLING FOR MODEL 'anon_model' NOW (CHAIN 4).
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(loo1 <- loo_subsample(fit1))
#>
#> Computed from 4000 by 400 subsampled log-likelihood
#> values from 572 total observations.
#>
#> Estimate SE subsampling SE
#> elpd_loo -529.4 25.9 0.4
#> p_loo 6.0 1.0 0.6
#> looic 1058.7 51.8 0.7
#> ------
#> MCSE of elpd_loo is 0.0.
#> MCSE and ESS estimates assume MCMC draws (r_eff in [0.8, 1.2]).
#>
#> All Pareto k estimates are good (k < 0.7).
#> See help('pareto-k-diagnostic') for details.
# model with an additional varying intercept for subjects
fit2 <- brm(rating ~ treat + period + carry + (1|subject),
data = inhaler)
#> Compiling Stan program...
#> Start sampling
#>
#> SAMPLING FOR MODEL 'anon_model' NOW (CHAIN 1).
#> Chain 1:
#> Chain 1: Gradient evaluation took 8.1e-05 seconds
#> Chain 1: 1000 transitions using 10 leapfrog steps per transition would take 0.81 seconds.
#> Chain 1: Adjust your expectations accordingly!
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#>
#> SAMPLING FOR MODEL 'anon_model' NOW (CHAIN 2).
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#> Chain 2: Gradient evaluation took 4.5e-05 seconds
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#> Warning: Bulk Effective Samples Size (ESS) is too low, indicating posterior means and medians may be unreliable.
#> Running the chains for more iterations may help. See
#> https://mc-stan.org/misc/warnings.html#bulk-ess
#> Warning: Tail Effective Samples Size (ESS) is too low, indicating posterior variances and tail quantiles may be unreliable.
#> Running the chains for more iterations may help. See
#> https://mc-stan.org/misc/warnings.html#tail-ess
(loo2 <- loo_subsample(fit2))
#> Warning: Some Pareto k diagnostic values are too high. See help('pareto-k-diagnostic') for details.
#> Warning: Some Pareto k diagnostic values are too high. See help('pareto-k-diagnostic') for details.
#> Warning: Some Pareto k diagnostic values are too high. See help('pareto-k-diagnostic') for details.
#>
#> Computed from 4000 by 400 subsampled log-likelihood
#> values from 572 total observations.
#>
#> Estimate SE subsampling SE
#> elpd_loo -524.1 27.0 2.9
#> p_loo 89.0 8.3 5.5
#> looic 1048.1 54.0 5.7
#> ------
#> MCSE of elpd_loo is NA.
#> MCSE and ESS estimates assume MCMC draws (r_eff in [0.2, 2.3]).
#>
#> Pareto k diagnostic values:
#> Count Pct. Min. ESS
#> (-Inf, 0.7] (good) 397 99.2% 104
#> (0.7, 1] (bad) 3 0.8% <NA>
#> (1, Inf) (very bad) 0 0.0% <NA>
#> See help('pareto-k-diagnostic') for details.
# compare both models
loo_compare(loo1, loo2)
#> Warning: Different subsamples in 'fit2' and 'fit1'. Naive diff SE is used.
#> elpd_diff se_diff subsampling_se_diff
#> fit2 0.0 0.0 0.0
#> fit1 5.3 37.4 2.9
# }