Mixed models, did someone figure out lme? [🇷 for BE/BA]

posted by d_labes  – Berlin, Germany, 2020-08-11 20:23 (1348 d 20:49 ago) – Posting: # 21858
Views: 2,200

Dear ElMaestro,

❝ ...

❝ For example: I prefer to play with variance components directly without involvement of rho (correlation) for the covariance of T and R. Where do I start? Playing around with weights, correlation structure, etc may get me what I want (see the two threads linked above), but that stil does not mean I am using lme meaningfully or optimally, I feel.


OK. That was my feeling in using Proc MIXED too.
And later on in the implementation via nlme/lme().

But life is no musical request programm ;-).
To have a stil you are satisfied with: Build your software by your own.

If I see your activity here in the forum (together with PharmCat) I think you will be able to do so. Contrary to me. Too small a brain to follow your posts. Even the easiest statements are out of my intellectual reach.

Thus I can't help. Sorry.

Regards,

Detlew

Complete thread:

UA Flag
Activity
 Admin contact
22,988 posts in 4,825 threads, 1,649 registered users;
31 visitors (0 registered, 31 guests [including 10 identified bots]).
Forum time: 17:13 CEST (Europe/Vienna)

As soon as we abandon our own reason, and are content
to rely upon authority, there is no end to our troubles.    Bertrand Russell

The Bioequivalence and Bioavailability Forum is hosted by
BEBAC Ing. Helmut Schütz
HTML5