Re: SV: OMEGA matrix

From: Jeroen Elassaiss-Schaap Date: October 02, 2014 technical Source: mail-archive.com
Hi everybody, Nice discussion! Good to hear that we seem to be in agreement on how to deal with off-diagonal elements. Thanks for all your feedback! I would like to underscore Mats comment about the expanded grid option. Also in my experience it seems to work very well, as an efficient approach to derive an omega block. Perhaps the loose end here is how to deal with the situation that Doug seems to encounter. Such cases (off-diagonal elements that worsen predictability) may be a signal of underlying processes or covariates that are not accounted for or not present in the dataset. Any better suggestions? Best regards, Jeroen http://pd-value.com -- More value out of your data!
Quoted reply history
On Oct 2, 2014, 6:43 PM, at 6:43 PM, Mats Karlsson <[email protected]> wrote: >Hi all, > >I agree with what Ken and Marc have said. On the point of a full matrix >as a diagnostic, which I think is good, an alternative is to run a >nonparametric estimation ($NONP) after your normal estimation. Even if >you did not use a full block in the original estimation, this step will >give you one (and it will “never” have estimation problems). It is not >entirely unproblematic to use as is, because sometimes a variance can >be biased due to an imposed diagonal structure in the preceding >parametric step, but will often result in informative results for how >to formulate an appropriate correlation structure. If you are >ambitious, you can use the extended grid option which I think is >recently implemented and addresses this problem. > >I haven’t had the experience of Douglas that adding additional >off-diagonal elements makes the simulation properties of a model worse. >The nonparametric option does allow a fuller description of the >correlation than the linear one though, so if that was the problem, >$NONP may offer a solution. > >Best regards, >Mats > > >Mats Karlsson, PhD >Professor of Pharmacometrics > >Dept of Pharmaceutical Biosciences >Faculty of Pharmacy >Uppsala University >Box 591 >75124 Uppsala > >Phone: +46 18 4714105 >Fax + 46 18 4714003 http://www.farmbio.uu.se/research/researchgroups/pharmacometrics/ > >Från: [email protected] >[mailto:[email protected]] För Ken Kowalski >Skickat: den 2 oktober 2014 17:10 >Till: [email protected]; 'Eleveld, DJ'; [email protected]; >[email protected]; [email protected]; 'Jeroen >Elassaiss-Schaap' >Ämne: RE: [NMusers] OMEGA matrix > >Hi All, > >I agree with everything that Marc and Douglas have pointed out. I too >do not advise building the omega structure based on repeated likelihood >ratio tests. The approach I take is more akin to what Joe had >suggested earlier using SAEM to fit the full block omega structure and >then look for patterns in the estimated omega matrix. Even with FOCE >estimation I will often fit a full block omega structure just to look >for such patterns. The full block omega structure may be >over-parameterized and sometimes may not even converge. Nevertheless, >as a diagnostic run it can be useful for uncovering patterns that may >lead to reduced omega structures with more stable model fits (i.e., not >over-parameterized). I’m not necessarily driven to find a parsimonious >omega structure as I’ll certainly err on the side of including >additional elements in omega provided there is sufficient support to >estimate these parameters (i.e., a stable model fit). For example, I >will select a full omega structure regardless of the magnitude of the >correlations if the model is stable and not over-parameterized. I have >no issue with those who want to identify a parsimonious omega >structure, however, I still maintain that a diagonal omega structure >often is not the most parsimonious. > >I also agree with Marc’s comment that we must judge parsimony relative >to the intended purpose of the model. If we are only interested in our >model to predict central tendency, then a diagonal omega structure may >be all that is needed. I would contend, however, that we often want to >use our models for more than just predicting central tendency. If we >perform VPCs, cross-validation, or external validations on independent >datasets, but the statistics we summarize to assess predictive >performance are only those involving central tendency then we’re not >really going to get a robust assessment of the omega structure. To >evaluate the omega structure we need to use VPC statistics that >describe variation and other percentiles besides the median. My >impression is that we aren’t as rigorous in our assessments of whether >our models can adequately describe the variation in our data. As I >stated earlier, I see so many standard VPC plots where virtually 100% >of the observed data are contained well within the 5th and 95th >percentiles. The presenter will often claim that these VPC plots >support the adequacy of the predictions but clearly the model is >over-predicting the variation. The over-prediction of the variation >may or may not be related to the omega structure as it could also be >related to skewed or non-normal random effect distributions. However, >if a diagonal omega structure was used and I saw this over-prediction >in the variation in a VPC plot, one of the first things I would do is >re-evaluate the omega structure and see if an alternative omega >structure can lead to improvements in predicting these percentiles. > >Best, > >Ken > >From: Gastonguay, Marc [mailto:[email protected]] >Sent: Thursday, October 02, 2014 7:03 AM >To: Eleveld, DJ; [email protected]<mailto:[email protected]>; >[email protected]<mailto:[email protected]>; >[email protected]<mailto:[email protected]>; >[email protected]<mailto:[email protected]>; Jeroen >Elassaiss-Schaap >Subject: Re: [NMusers] OMEGA matrix > >Douglas makes important point in this discussion. That is, the method >used to judge parsimony of the model must consider the performance of >the model for intended purpose. > >Consider the parsimony principle: "all things being equal, choose the >simpler model". The key is in how to judge the first part of that >statement. > >A model developed based on goodness of fit metrics such as AIC, BIC, or >repeated likelihood ratio tests, may be the most parsimonious model for >predicting the current data set. This doesn't ensure that the model >will be "equal" in performance to more complex models for the purpose >of predicting the typical value in an external data set - external >cross validation might be required for that conclusion. Further, if the >purpose is to develop a model that is a reliable stochastic simulation >tool, a simulation-based model checking method should be part of the >assessment of "equal" performance when arriving at a parsimonious >model. > >Since most of our modeling goals go far beyond prediction of the >current data set, it's necessary to move beyond metrics solely based on >objective function and degrees of freedom when selecting a model. In >other words, it may be perfectly fine (and even parsimonious) for a >model to include more parameters than the likelihood ratio test tells >you to, if those parameters improve performance for the intended >purpose. > >Best regards, >Marc
Oct 02, 2014 Mats Karlsson SV: OMEGA matrix
Oct 02, 2014 Jeroen Elassaiss-Schaap Re: SV: OMEGA matrix