lme4 convergence/numerical issue with large sample 2 level logit
doug, thanks for your reply. i do tons of mixed modeling, so obviously am a big fan of / highly dependent on your work. results from:
sessionInfo()
R version 2.13.0 (2011-04-13) Platform: i386-pc-mingw32/i386 (32-bit) locale: [1] LC_COLLATE=English_United States.1252 [2] LC_CTYPE=English_United States.1252 [3] LC_MONETARY=English_United States.1252 [4] LC_NUMERIC=C [5] LC_TIME=English_United States.1252 attached base packages: [1] stats graphics grDevices utils datasets methods base other attached packages: [1] MCMCglmm_2.12 corpcor_1.5.7 ape_2.7-1 coda_0.14-4 [5] tensorA_0.36 lme4_0.999375-39 Matrix_0.999375-50 lattice_0.19-23 [9] nlme_3.1-100 foreign_0.8-43 loaded via a namespace (and not attached): [1] gee_4.13-16 grid_2.13.0 stats4_2.13.0 tools_2.13.0 i apologize for trying MCMCglmm, feel like i have lipstick on my collar (ha!). Please do tell me how to install "lme4a", I have downloaded the zip file for windows (https://r-forge.r-project.org/bin/windows/contrib/latest/lme4a_0.999375-66.zip), but haven't figured out how to load it into working session of R. also, could you point me in the right direction for start values? would it appreciably help optimization to use results from random intercept only model as starts for fixed effects and random intercept variance estimate? also, what do you think of "glmmPQL"? does that yield decent estimates for models of my level of size/complexity? Thx for any help. D
On Fri, May 27, 2011 at 2:14 PM, <dmbates at gmail.com> wrote:
On Thu, May 26, 2011 at 8:53 PM, Daniel Adkins <deadkins at vcu.edu> wrote:
hi all, trying to fit either this model: proto1 <- lmer(hibpe ~ age + b + b_age + h + h_age + female + female_age + bxf + hxf + numwaves + dead + nodoctor + nohosp ? ? ? ?+(1|hhidpn) +(0 + age | hhidpn) , ?nAGQ =300, family=binomial, data=hrs_data, na.action =na.omit, ?verbose=TRUE) or the same model allowing correlation btwn the REs: proto2 <- lmer(hibpe ~ age + b + b_age + h + h_age + female + female_age + bxf + hxf + numwaves + dead + nodoctor + nohosp ? ? ? ?+ (age | hhidpn) , ?nAGQ =300, family=binomial, data=hrs_data, na.action =na.omit, ?verbose=TRUE) it is big data: ~50K obs & ~8400 clusters (subjects, in this case). when i try to fit these models they run ~forever (>72 hours) with no convergence. when i try a laplace approx for the quadrature (i.e., nAGQ=1) I get false convergence. I can successfully fit a slightly less complex model in which everything is the same except dropping the age RE: proto2 <- lmer(hibpe ~ age + b + b_age + h + h_age + female + female_age + bxf + hxf + numwaves + dead + nodoctor + nohosp ? ? ? ?+ (1 | hhidpn) , ?nAGQ =300, family=binomial, data=hrs_data, na.action =na.omit, ?verbose=TRUE) this takes ~25 minutes to converge, and it gives an accurate solution (cross-validated in stata via xtlogit and (for fixed effects) using simple, single level logit). notably, i only get global optimum convergence once I set nAGQ>200.
nAGQ > 200 ? ?That seems rather drastic when you have an average of 6 observations per subject. The problem may be related to the optimizer. ?The development version of the package, called lme4a, uses another optimizer that has, in most but not all cases, been faster and more reliable. ?You may want to try that version of the package instead. ?If you can tell us what platform you are using, say by providing the output of sessionInfo() we should be able to provide you with installation instructions for lme4a (although I think that installation on Mac OS X is still not straightforward).
Obviously, the estimation of the 2nd RE is the issue and a very difficult numerical problem given data size/structure. Stata (xtmelogit) just conks out almost immediately and says that it doesn't have the memory to handle the quadrature optimization (not in so many words, but still), even with memory maxed out for the program/hardware. Any suggestions for shortcuts to make 'proto1' or 'proto2' estimate? i am about to have to resort to BUGS, which will take eons, but at least will eventually give decent estimates. Would strongly prefer sticking with R though. Start values maybe? Would that help? Any code for inputting these (i have never done it before in R)? nlme? hglm? I am desperate/open to any suggestions. Thx, D -- Daniel E. Adkins, PhD Assistant Professor Center for Biomarker Research and Personalized Medicine School of Pharmacy Virginia Commonwealth University McGuire Hall, Room 216B 1112 East Clay Street Richmond, VA 23298
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Daniel E. Adkins, PhD Assistant Professor Center for Biomarker Research and Personalized Medicine School of Pharmacy Virginia Commonwealth University McGuire Hall, Room 216B 1112 East Clay Street Richmond, VA 23298