similar to: Ancova and lme use

Displaying 20 results from an estimated 900 matches similar to: "Ancova and lme use"

2005 Dec 05
0
Use of lme() function
Dear R-users, We expect to develop statistic procedures and environnement for the computational analysis of our experimental datas. To provide a proof of concept, we plan to implement a test for a given experiment. Its design split data into 10 groups (including a control one) with 2 mesures for each (ref at t0 and response at t1). We aim to compare each group response with control response
2005 Nov 25
1
covariance analysis by using R
Hi, Is anyone has solved MR Xin Meng problem (see below) ? We have the same analysis configuration : 10 groups (including control one) with 2 mesures for each (ref at t0 and response at t1). We expect to compare each group response with control response (group 1) using a multiple comparison procedure (Dunnett test). In order to perform this test, we have to normalize our data (as you) to
2006 Jan 11
1
Homogenic groups generation - Randomisation
Dear R-users, We expect to create N homogenic groups of n features from an experimentation including N*n mesures. The aim of this is to prevent from group effects. How to do that with R functionalities. Does anyone know any methodes enabling this ? Best regards. Alexandre MENICACCI Bioinformatics - FOURNIER PHARMA 50, rue de Dijon - 21121 Daix - FRANCE a.menicacci at fr.fournierpharma.com t??l
2006 Jan 16
1
Homogenous groups building - Randomisation
Dear R-users, We expect to form N homogeneous groups of n features from an experimentation including N*n data. The aim is to prevent group effects. How to do that with R functionalitites ? Does anyone know any way enabling this ? Example : 100 patients are observed. 3 biochemical parameters are mesured for each one (Red and white globules ans glycemia). Patient RG RW
2006 Mar 07
2
Building tkentry dynamicly
Dear R-users, I would like to build N "tkentry" compounds in the same window, with default text for each. As N is variable I need to construct them in an iterative way : library(tcltk) main<-tktoplevel() tktitle(main)<-"My Tool" filenames<-c("toto","tata","titi") N<-length(filenames) for (i in 1: N) {
2004 May 20
4
pmvt problem in multcomp
Hi, all: Two examples are shown below. I want to use the multiple comparison of Dunnett. It succeeded in upper case "example 1". However, the lower case "example 2" went wrong. In "example 2", the function pmvt return NaN, so I cannot show this simtest result. Is there any solution? (I changed the variable "maxpts" to a large number in front of the
2004 Aug 13
5
simtest for Dunnett's test
Hi! I use simtest fonction of multcomp package to compile a Dunnett's test. I have 10 treatments and one control group, so i create a matrix with: m<-matrix(0,10,11) m[1,1]<--1 m[1,2]<-1 m[2,1]<--1 m[2,3]<-1 m[3,1]<--1 m[3,4]<-1 m[4,1]<--1 m[4,5]<-1 m[5,1]<--1 m[5,6]<-1 m[6,1]<--1 m[6,7]<-1 m[7,1]<--1 m[7,8]<-1 m[8,1]<--1 m[8,9]<-1
2002 Jan 07
3
compiling packages
Hello, happy new year to all. The new Year gave me a new computer with Win98 and promptly I installed R on it. I created a directory R, with subdirectories gcc, perl,bin, helpwrk and rw1040. I got rw1040 from BDR place, the rest were gotter from the internet in the last week of the year, i.e. they are the newest versions. I modified autoexec.bat to put gcc\bin, perl\bin, etc in the path. I put the
2013 Oct 27
1
dunnett test questions
Hi, I've got a data set with a control group and a number of experimental groups, that have unequal sample sizes, and am measuring the number of people in each that respond yes or no. I'd like to use a dunnett test in R, where the syntax is supposed to be like: library(multcomp) test.dunnett=glht(anova_results,linfct=mcp(method="Dunnett")) confint(test.dunnett)
2002 Jun 26
2
contrast matrix in package multcomp
Hi, I've got a problem building a contrast matrix for the Dunnet contrast in package multcopm. The following works fine: > summary(simtest(adiff ~ trial)) Simultaneous tests: Dunnett contrasts Data: adiff by trial Contrast matrix: trial1 trial2 trial3 trial4 trial5 trial2-trial1 -1 1 0 0 0 trial3-trial1 -1 0 1 0 0
2013 Feb 26
1
Getting the correct factor level as Dunnett control in glht()
Hello all, I would like to do a Dunnett test in glht(). However, the factor level I want to use as the control is not the first. dunn1<-glht(model3, linfct = mcp(Container = "Dunnett"), alternative = "less") The factor container has 8 levels, so it would be nice not to manually enter in all of the contrasts. I originally discovered glht() when working with a glm model
2007 Feb 09
1
Help in using multcomp.
Hi All, I am trying use 'multcomp' for multiple comparisons after my ANOVA analysis. I have used the following code to do ANOVA: dat <- matrix(rnorm(45), nrow=5, ncol=9) f <- gl(3,3,9, label=c("C", "Tl", "T2")) aof <- function(x) { m <- data.frame(f, x); aov(x ~ f, m) } amod <- apply(dat,1,aof) Now, how can I use
2006 Mar 08
0
survival
Dear R-helpers, We marked 6000 leaves from 5 SPECIES - 10 individuals/species - in two different TREATMENTs: a control and a dry-plot from which 50% of incoming precipitation was excluded. We followed those leaves for 42 months and noted the presence and absence at each visit. I then carried out a Cox Harzard model to see differences in leaf mortality between parcels and among species over time:
2008 Sep 03
2
ANCOVA/glm missing/ignored interaction combinations
Hi I am using R version 2.7.2. on a windows XP OS and have a question concerning an analysis of covariance with count data I am trying to do, I will give details of a scaled down version of the analysis (as I have more covariates and need to take account of over-dispersion etc etc) but as I am sure it is only a simple problem but I just can't see how to fix it. I have a data set with count
2007 Nov 21
1
question about multiple comparison in ANOVA
I am not sure whether there is a bug. When I tested the example given for "glht" in the help, I entered the following error: Running commands: amod <- aov(minutes ~ blanket, data = recovery) rht <- glht(amod, linfct = mcp(blanket = "Dunnett"), alternative = "less") Errors are: Error in try(coef.(model)) : could not find function
2007 Nov 21
1
multiple comparison (glht) problem
I am not sure whether there is a bug. When I tested the example given for "glht" in the help, I entered the following error: Running commands: amod <- aov(minutes ~ blanket, data = recovery) rht <- glht(amod, linfct = mcp(blanket = "Dunnett"), alternative = "less") Errors are: Error in try(coef.(model)) : could not find function
2011 May 24
3
test de Friedman , con comparación planificada simple (la primera contra el resto...).
Hola. Hay alguna función que haga un Friedman test (digamos 4 tratamientos o tiempos relacionados/dependientes) y que después haga una comparación de un tratamiento contra el resto, digamos el primero, como un contratase simple, o un Dunnett? o simplemente ¿como hago un Dunnett para unos tratamientos relacionados? -- Antonio M [[alternative HTML version deleted]]
2010 Mar 15
1
Multiple comparisons for a two-factor ANCOVA
I'm trying to do an ANCOVA with two factors (clipping treatment with two levels, and plot with 4 levels) and a covariate (stem diameter). The response variable is fruit number. The minimal adequate model looks like this: model3<-lm(fruit~clip + plot + st.dia + clip:plot) I'd like to get some multiple comparisons like the ones from TukeyHSD, but TukeyHSD doesn't work with the
2005 May 15
3
adjusted p-values with TukeyHSD?
hi list, i have to ask you again, having tried and searched for several days... i want to do a TukeyHSD after an Anova, and want to get the adjusted p-values after the Tukey Correction. i found the p.adjust function, but it can only correct for "holm", "hochberg", bonferroni", but not "Tukey". Is it not possbile to get adjusted p-values after
2002 Jun 20
1
new package `multcomp'
New package `multcomp' for general multiple comparisons written by Frank Bretz, Torsten Hothorn and Peter Westfall We've uploaded the package `multcomp' to CRAN. The R package allows for multiple comparisons of k groups in general linear models. We use the unifying representations of multiple contrast tests, which include all common multiple comparison procedures, such as the