similar to: lmer with 2 random effects with only two levels

hi all how we can do get and post value. i made one form and in this form their is two field loginname and password.and when i click on submit button than i t should verify from database and than the next page will arrive .how i can do that. how i can post value and than get it from that from and check .plese tell me yhis all in rubyon rails. hope for reply bye

Hi R experts, I have been using ReML as follows... model<-lmer(late.growth~mtf+year+treat+hatch.day+hatch.day:year+hatch.day:treat+ mtf:treat+ treat:year+ year:treat:mtf+(1|fybrood), data = A) then I wanted to plot the results of the three way interaction using lines() as follows... tmp<-as.vector(fixef(model)) graph1<-plot(mtf,fitted(f2), xlab=list("Brood Size"),

Hi all, Two questions: 1. Is there a way to evaluate models from lmer() with a poisson distribution? I get the following error message: library(lme4) lmer(tot.fruit~infl.treat+def.treat+(1|initial.size),family=poisson)->model plot(fitted(model),resid(model)) Error: 'resid' is not implemented yet Are there any other options? 2. Why doesn't the function estimable() in gmodels

On Apr 16, 2008, at 2:50 AM, heisenbug wrote: > > And now here is my educated speculation: > There are 2 things that became slower > 1) Use::getUser() > 2) Use::get/set due to tagging. > > The former is seldom called: > > $ find lib -name "*.cpp" | xargs grep "getUser(" | wc -l > 41 The majority of those aren't actually Use::getUser, but

fixed @ R-forge. New version should appear on CRAN soon. Thanks for the report! Torsten > > ---------- Forwarded message ---------- > Date: Sat, 3 Sep 2011 23:56:35 +0200 > From: Ulrich Halekoh <Ulrich.Halekoh at agrsci.dk> > To: "r-help at r-project.org" <r-help at r-project.org> > Subject: [R] glht (multcomp): NA's for confidence intervals using

Hej, Calculation of confidence intervals for means based on a model fitted with lmer using the package multcomp - yields results for calpha=adjusted_calpha - NA's for calpha=univariate_calpha Example: library(lme4) library(multcomp) ### Generate data set.seed(8) d<-expand.grid(treat=1:2,block=1:3) e<-rnorm(3) names(e)<-1:3 d$y<-rnorm(nrow(d)) + e[d$block]

This concerns whether p-values from lmer can be trusted. From simulations, it seems that lmer can produce very small, and probably spurious, p-values. I realize that lmer is not yet a finished product. Is it likely that the problem will be fixed in a future release of the lme4 package? Using simulated data for a quite standard mixed-model anova (a balanced two-way design; see code for the

On Apr 16, 2:13 am, Dan Gohman <goh... at apple.com> wrote: > Hi Gabor, > > Can you provide performance data for this? I'd > like to know what affect these changes have on > compile time. Hi Dan, Unfortunately, no. I can feed you with some speculation, though, see below. The reason why I cannot do measurements (at the moment) is that - I have no experience with

For block effects with small variance, lmer will sometimes estimate the variance as being very close to zero and issue a warning. I don't have a problem with this -- I've explored things a bit with some simulations (see below) and conclude that this is probably inevitable when trying to incorporate random effects with not very much data (the means and medians of estimates are plausibly

Dear all, I have some growth curve data from an experiment that I try to fit using lm and lmer. The curves describe the growth of classification accuracy with the amount of training data t, so basically y ~ 0 + t (there is no intercept because y=0 at t0) Since the growth is somewhat nonlinear *and* in order to estimate the treatment effect on the growth curve, the final model is y ~ 0 + t +

Hello I'm working with mixed effects models using lmer() and have some problems to get all variance components of the model's random effects. I can get the variance of the random effect out of the summary and use it for further calculations, but not the variance component of the residual term. Could somebody help me with that problem? Thanks a lot! Below an example. Aline ## EXAMPLE

Hello, In a study exploring transgenerational transmission of anxiety disorder we investigate whether infants react to experimentally induced mood changes of their mothers. We measured the time that an infant needed to cross a cliff (=crossing time) depending on whether his mother had previously undergone a mood induction (treatment) or not (control). The treatment is thus a

Dear all, I was wondering if anyone could help solve a problem of a missing interaction effect!! I carried out a 2 x 2 factorial experiment to see if eggs from 2 different locations (Origin = 1 or 2) had different hatching success under 2 different incubation schedules (Treat = 1 or 2). Six eggs were taken from 10 females (random = Female) at each location and split between the treatments,

Ronaldo, Further to my previous posting on your Glycogen nested aov model. Having read Douglas Bates' response and Reflected on his lmer analysis output of your aov nested model example as given.The Glycogen treatment has to be a Fixed Effect.If a 'treatment' isn't a Fixed Effect what is ? If Douglas Bates' lmer model is modified to treat Glycogen Treatment as a purely

Your response nicely clarifies a question that I've had for a long time, but which I've dealt with by giving each subject a unique label. Unless I'm missing something, both techniques should work as the toy example below gives exactly the same output in all 3 cases below (forgetting about the convergence problem). Would there be a reason to prefer labeling the levels one way or

Dear R users, Prof. Ripley just corrected my understanding of the use of weights in glm, which I thought would allow me to correctly use lmer. However I'm still having problems. My data takes the form of # of infected and uninfected individuals that were measured over time under different treatments. I'm using lmer to adjust for the repeated measures over time. In fitting the

Hi, I am new to this list. I have a question regarding including both spatial and temporal random factors in lmer. These two are not nested, and an example of model I try to fit is model1<-lmer(Richness~Y+Canopy+Veg_cm+Treatment+(1|Site/Block/Plot)+(1|Year), family=poisson, REML=FALSE), where richness = integer Y & Treatment = factor Canopy & Veg_cm = numerical, continous

Hi Ralf, I tried the following > install.packages("RCurl") which went OK, but then same story when I tried to install tseries. > sessionInfo() R version 3.6.1 (2019-07-05) Platform: x86_64-pc-linux-gnu (64-bit) Running under: Debian GNU/Linux 10 (buster) Matrix products: default BLAS: /usr/lib/x86_64-linux-gnu/blas/libblas.so.3.8.0 LAPACK:

Hi I have data from an experiment that used a repeated-measures factorial 2x2 design (i.e. each participant contributed data to both levels of both factors). I need a non-parametric version of the repeated-measures factorial ANOVA to analyse the data. SPSS only has non-parametric tests for one-way ANOVAs but I have been told that the test I need can be implemented using the R software.

Dear R-help-list, I have a problem in which the explanatory variables are categorical, the response variable is a proportion, and experiment contains technical replicates (pseudoreplicates) as well as biological replicated. I am new to both generalized linear models and mixed- effects models and would greatly appreciate the advice of experienced analysts in this matter. I analyzed the