similar to: mcmcsamp shortening variable names; how can i turn this feature off?

I've been trying to keep track with lmer, and now I have a couple of questions with the latest version of Matrix (0.995-4). I fit 2 very similar models, and the results are severely rounded in one case and rounded not at all in the other. > y <- 1:10 > group <- rep (c(1,2), c(5,5)) > M1 <- lmer (y ~ 1 + (1 | group)) > coef(M1) $group (Intercept) 1 3.1 2

Dear r-helpers, I can run the examples on the mcsamp help page. For example: **************************************** > M1 <- lmer (y1 ~ x + (1|group)) > (M1.sim <- mcsamp (M1)) fit using lmer, 3 chains, each with 1000 iterations (first 500 discarded) n.sims = 1500 iterations saved mean sd 2.5% 25% 50% 75% 97.5% Rhat n.eff beta.(Intercept)

Hello, R community, I have been using the lmer and mcmcsamp functions in R with some difficulty. I do not believe this is my code or data, however, because my attempts to use the sample code and 'sleepstudy' data provided with the lme4 packaged (and used on several R-Wiki pages) do not return the same results as those indicated in the help pages. For instance: > sessionInfo() R

Hello, I am a chemical student and I make use of 'lme/lmer function' to handle experiments in split-plot structures. I know about the mcmcsamp and I think that it's very promissory. I would like knowing "the concept behind" of the mcmcsamp function. I do not want the C code of the MCMCSAMP function. I would like to get the "pseudo-algorithm" to understanding that

Dear All, I've been using mcmcsamp() successfully with a few different mixed models but I can't get it to work with the following. Is there an obvious reason why it shouldn't work with a model of this structure ? *brief summary of objective: I want to test the effect of no-fishing marine reserves on the abundance of a target species. I have samples at coral reef sites inside and

Hi, I have fitted a generalized linear mixed effects model using lmer (library lme4), and the family = quasibinomial. I have tried to obtain a MCMC sample, but on calling mcmcsamp(model1, 1000) I get the following error which I don't understand at all: Error in .local(object, n, verbose, ...) : Update not yet written traceback() delivers: 4: .Call(mer_MCMCsamp, ans, object) 3:

I've got a problem with "mcmcsamp" used with glmer objects produced with "lmer" from the lme4 package. When calling mcmcsamp, I get the error Error in if (var(y) == 0) { : missing value where TRUE/FALSE needed This does not occur with all models, but I can't find anything wrong with the dataset. If the error is in my data, can someone tell me what I am looking

Dear all, I am running a mixed model using lmer. In order to obtain CI of individual coefficients I use mcmcsamp. However, I need advice which values that are most appropriate to present in result section of a paper. I have not used mixed models and lmer so much before so my question is probably very naive. However, to avoid to much problems with journal editors and referees addicted to

Hi, I've got a linear mixed model created using lmer: A6mlm <- lmer(Score ~ division + (1|school), data=Age6m) (To those of you to whom this model looks familiar, thanks for your patience with this & my other questions.) Anyway, I was trying this to look at the significance of my fixed effects: A6post <- mcmcsamp(A6mlm, 50000) library(coda) HPDinterval(A6post) ..but I got this

I really hope sombody could help me with the following, I'm having problems accessing the random effect samples following the example on MCMCsamp: (fm1 <- lmer(Reaction ~ Days + (1|Subject) + (0+Days|Subject), sleepstudy)) set.seed(101); samp0 <- mcmcsamp(fm1, n = 1000, saveb=TRUE) str(samp0) Formal class 'merMCMC' [package "lme4"] with 9 slots ..@ Gp :

I've searched the help archives of both lists and apologize if I missed the answer to my question: Is there an update on developing mcmcsamp for glmer? I'm using R v. 2.7.2 (on our Unix server - will hopefully be updated soon) and 2.8.1 on my PC and get the message for both: gm1 <- glmer(cbind(incidence, size - incidence) ~ period + (1 | herd),family = binomial, data = cbpp)

Hi! I have samba 3 beta2 as PDC. Now I need to make all mebers of the unix grop "users" local admins on their Windows systems, because Wordperferct 8 doesn't run otherwise. As the "domain admin group" setting from smb.conf doen't exist anymore, I don't know, how to do the group mapping correctly. Could someone explain the steps to do it? Thanks in advance for

Hi, I would appreciate help with the following model <<1>>= gunload <- read.table(hh('datasets/gunload.dat'), header = T) gunload$method <- factor(gunload$method, labels = c('new', 'old')) gunload$physique <- factor(gunload$group, labels = c('slight', 'average', 'heavy')) gunload$team9 <- factor(rep(1:9, each = 2)) @ This

I'm fitting a GLMM to some questionnaire data. The structure is J individuals, nested within I areas, all of whom answer the same K (ordinal) questions. The model I'm using is based on so-called continuation ratios, so that it can be fitted using the lme4 package. The lmer function fits the model just fine, but using mcmcsamp to judge the variability of the parameter estimates produces

Hello, I'm building a couple of mixed models using the lmer function. The actual modelling is going well, but doing some reading on the use of crossed random effects and the comparison of models with and without random effects it is clear that I need to generate some Markov Chain Monte Carlo samples. However, I'm struggling because everyone time I go to generate a sample I get the

Hi folks, I have assumed that ratios of variance components (Fst and Qst in population genetics) could be estimated using the output of mcmcsamp (the series on mcmc sample estimates of variance components). What I have started to do is to use the matrix output that included the log(variances), exponentiate, calculate the relevant ratio, and apply either quantile or or HPDinterval to get

(To the list moderator: I just subscribed to the list. Apologies for not having done so longer before trying to post.) Hi all, I am currently using lmer to analyze data from an experiment with a single fixed factor (treatment, 6 levels) and a single random factor (block). I've been trying to follow the online guidance for estimating p-values for parameter estimates on these and other

Thanks to some help by Doug Bates (and the updated version of the Matrix package), I've refined my question about fitting nested and non-nested factors in lmer(). I can get it to work in linear regression but it crashes in logistic regression. Here's my example: # set up the predictors n.age <- 4 n.edu <- 4 n.rep <- 100 n.state <- 50 n <- n.age*n.edu*n.rep age.id

How can I get prediction intervals from a mixed-effects model? Consider the following example: library(nlme) fm3 <- lme(distance ~ age*Sex, data = Orthodont, random = ~ 1) df3.1 <- with(Orthodont, data.frame(age=seq(5, 20, 5), Subject=rep(Subject[1], 4), Sex=rep(Sex[1], 4))) predict(fm3, df3.1, interval='prediction') # M01 M01

Ok, Here is what I got working: A call comes in from a Zap line. 5 SIP extension ring if nobody picks up, the call is transfered to a cell phone number. That works. I not want to add a playback of a file ("Please waite while you are being transfered") before transfering the call to the cell phone. How can I do this? Andre