similar to: model set up question

My apologies, I forgot to CC: to the list on my previous communication with Daniel. Jesse ----- Forwarded by Jesse Albert Canchola/EMVL/DIAG/US/BAYER on 08/21/2006 10:50 AM ----- Jesse Albert Canchola/EMVL/DIAG/US/BAYER 08/21/2006 09:36 AM To "Daniel Nordlund" <res90sx5 at verizon.net> cc Subject RE: [R] Permutations with replacement Thanks, Daniel. I need to enumerate

dfhfsdhf at ghghgr.com I ran a simple lme model: modelrandom=lmer(y~ (1|Test) + (1|strain), data=tempsub) Extracted the BLUPs: blups=ranef(modelrandom)[1] Even wrote myself a nice .csv file....: write.csv(ranef(modelrandom)[1],paste(x,"BLUPs.CSV")) This all works great. I end up with a .csv file with the names of my strains in the first column and the BLUP in the second

hello everyone, I would like to as for advice for the use of ?lmer? (package ?lme4?) and writing the proper syntax to best describe my data using a mixed-effects model. I have just started to use these models, and although I have read some good examples (Extending the Linear Model with R, Faraway 2005; and the R book, Crawley 2007), I am still not sure of the syntax to test my hypothesis.

I've scoured the archives but have found no concrete answer to my question. Problem: Two data sets 1st data set(x) = 20,000 rows 2nd data set(y) = 5,000 rows Both have the same column names, the column of interest to me is a variable called strain. For example, a strain named "Chab1405" appears in x 150 times and in y 25 times... strain "Chab1999" only appears 200

Dear R user, I have a question on using R to analyze data with repeated measurements. I have 2 species with several strains (12) per species, each of which has been measured twice with for a given trait. No particular covariance, just two measures. Now I want to analyze the data with an ANOVA (aov) considering these repeated measures to get the MSq and SSq for the species and strain level. I

Dear R users, Here is the coxme output I obtain on my survival dataset having 3 strains and 2 infection status (i: infected, ni: non infected) coxme(Surv(lay) ~ infection*strain, data=datalay, random= ~1 |block) Cox mixed-effects model fit by maximum likelihood Data: datalay n= 1194 Iterations= 3 77 NULL Integrated Penalized Log-likelihood -7270.028 -7223.859 -7218.175

Dear List, I downloaded R for the first time yesterday, in the hopes that I might deal more effectively with a complex repeated measures experimental design involving inbred strains of laboratory mice. The design below, somewhat simplified, cannot be computed with standard ANOVA, because something called the X'X matrix is too large. The design has the following factors: Between-subject

Hello there, I''m having lots of problems with my setup here. Let me explain: I am network administrator for my university dorm. We are about 300 users, and we have 2 ADSL connections doing load balancing with 300kbits upstream and 2Mbit downstream. The load balancing is working great, we are doing connection tracking so I can mark and hence prioritize interactive traffic and ACKS

Dear list, Has anyone created a version of SSmicmen that allows testing for group differences? The basic Michaelis-Menten equation is: (Bmax * X) / (Kd + X). The nlme package allows modeling of random effects for Bmax and Kd as needed, but I curious how I can build in group differences? I have receptor binding data for strains of mice, and following Pinheiro and Bates' lead in their

Good morning, I'm trying to write a function to assign the mean separation grouping letters to the factors of an experiment. A client wants this so I thought I'd write my own function for future use. But I'm having trouble doing it because I don't understand the logic of the assignment. As a general example, consider the following data and the results from SAS and its weak

I have assayed the concentrations of various metal elements in different anatomic regions of two strains of mice. Now, for each element, in each region, I want to do a t test to find whether there is any difference between the two strains. Here is what I did (using simulated data as an example): # create the data frame > elemconc = data.frame(expand.grid(id=1:3, geno=c('exp',

inputfille snpid indid genotype gvariable probeid gene geneexpression rs1040480 CHB_NA18524 C/T 2 GI_19743926-I PTPRT 5.850586 rs1040480 CHB_NA18526 C/C 1 GI_19743926-I PTPRT 6.028641 rs1040480 CHB_NA18529 C/C 3 GI_19743926-I PTPRT 5.944392 rs1040481 CHB_NA18532 C/C 1 GI_19743926-I PTPRT 5.938578 rs1040481 CHB_NA18537 C/C 2 GI_19743926-I PTPRT 5.874439 rs1040481 CHB_NA18540 C/C 3 GI_19743926-I

Has anyone programmed condition indexes in R? I know that there is a function for variance inflation factors available in the car package; however, Belsley (1991) Conditioning Diagnostics (Wiley) notes that there are several weaknesses of VIFs: e.g. 1) High VIFs are sufficient but not necessary conditions for collinearity 2) VIFs don't diagnose the number of collinearities and 3) No one has

Dear R-ers, I am currently running some Wilcoxon tests in R-64. How do I find the degrees of freedom in the output I am receiving? > wilcox.test(good$TRUE, good$x4a, paired=FALSE) Wilcoxon rank sum test with continuity correction data: good$TRUE and good$x4a W = 2455, p-value < 2.2e-16 alternative hypothesis: true location shift is not equal to 0 Thank you, Stephen.

Dear all, I have some questions regarding the validity an implementation of statistical tests based on linear models and loess. I've searched the R-help arhives and found several informative threads that related to my questions, but there are still a few issues I'm not clear about. I'd be grateful for guidance. Background and data set: I wish to compare the growth and metabolism

Dear ALL I don't know why I can see this error in run this sentences. In paste("V", 1L:cols, sep = "") : NAs introduced by coercion DATA<-read.delim ("D:\\DATA\\GeneExpression.txt",header=FALSE) I will be glad if you help me. Best Regards, Stat Consult [[alternative HTML version deleted]]

We need to keep the discussion on the list. When I run your code, there are several problems. strain.data <- read.xlsx("Dee rhiz.xlsx", sheetName ="strain", header = T, row.names = 1) str(strain.data) # lists 9 columns at the end with all NAs strain.data1 <- (strain.data, sqrt.dist = TRUE) # this is not a valid R line. I get Error: unexpected ',' in

Dear users, i'm using the sem package in R, because i need to improve a confermative factor analisys. I have so many questions in my survey, and i suppose, for example, that Question 1 (Q1) Q2 and Q3 explain the same thing (factor F1), Q4,Q5 and Q6 explain F2 and Q7 and Q8 explain F3... For check that what i supposed is true, i run this code to see if the values of loadings are big or not.

I have data in a file named hands.dat, which is given at the end of this question. (It's from a stats textbook example on anova). I'd like to do an aov on this, which I guess would be d <- read.table("~/hands.dat", header=TRUE) aov(Bacterial.Counts ~ Water + Soap + Antibacterial.Soap + Alcohol.Spray, data=d) but this fails. Do I need to break d$Method up into columns for

In the vcdExtra package on R-Forge, I have functions and generic methods for calculating log odds ratios for R x C x strata tables. I'd like to define methods for fitting weighted lm()s to the resulting loddsratio objects, but I'm having problems figuring out how to do this generally. # install.packages("vcdExtra", repos="http://R-Forge.R-Project.org")