similar to: analysing mixed effects/poisson/correlated data

Hi Folks, I have repeated measures for data on association time (under 2 acoustic condtions) in male and female frogs as they grow to adulthood (6 timepoints). Thus, two within-subject variables (Acoustic Condition: 2 levels, Timepoint: 6 levels) and one between-subject variable (Sex:male or female). I am pretty sure my distributions depart from normality but I would first like to simply run a

Hi, I'm having difficulty importing my textfile that looks something like this: #begin text file Timepoint 1 ObjectNumber Volume SurfaceArea 1 5.3 9.7 2 4.9 8.3 3 5.0 9.1 4 3.5 7.8 Timepoint 2 ObjectNumber Volume SurfaceArea 1 5.1

I am executing a Repeated Measures Analysis of Variance with 1 DV (LOCOMOTOR RESPONSE), 2 Within-Subjects Factors (AGE, ACOUSTIC CONDITION), and 1 Between-Subjects Factor (SEX). Does anyone know whether the between-subjects factor (SEX) belongs in the Error Term of the aov or not? And if it does belong, where in the Error Term does it go? The 3 possible scenarios are listed below: e.g., 1.

dear list, i am using a multifactorial design with two treatments (factor A: drugs, three levels; factor B: theraphy, two levels) and a time factor (three levels, different timepoint). hypothetically, i measured the same subjects for all treatements and timepoints, so its a repeated measurement design. now i ran an anova in R and also some Tukey post-hoc tests using glht. but what i am actually

dear list, i am running a within-design ANOVA with 4 factors (4,4,2 and 2 levels each). the last one is a time factor comprising two different treatment timepoints. i fit a mixed-effects model using lme and apply the anova function to the outcome. according to this analysis, there are highly significant main effect on the first and the time factor. i then checked the boxplots for the two 4-level

Hello, I have a number of files output1.dat, output2.dat, ... , output20.dat, each of which monitors several variables over a fixed number of timepoints. From this I want to create a data frame which contains the mean value between all files, for each timepoint and each variable. The code below works, but it seems like I should be able to do the second part without a for loop. I played

library(ggplot2) a<- read.table("data", header=T) b = na.omit(a) ggplot(data=b) + geom_line(aes(x=timepoint, y=value,group=sample, colour= factor(sample))) +? geom_point(aes(x=timepoint, y=value, group=s ample)) + facet_wrap(~bio, scales = "free",ncol = 5) +theme_bw() + opts(legend.direction = "horizontal",??? legend.position = "top",????

What is the best way to report the standard error when publishing Kaplan-Meier plots? In my field (Vascular Surgery), practitioners loosely refer to the "10% error" cutoff as the point at which to stop drawing the KM curve. I am interpreting this as the *standard error of the cumulative hazard*, although I'm having a difficult time finding some guidelines about this (perhaps I am

System: R 2.3.1 on a Windows XP computer. I am validating several cancer prognostic models that have been published with a large independent dataset. Some of the models report a probability of survival at a specified timepoint, usually at 5 and 10 years. Others report only the linear predictor of the Cox model. I have used Harrell's c index for censored data (rcorr.cens) as a measure of

Hi, I cannot find a 'vectorized' solution to this 'for loop' kind of problem. Do you see a vectorized, fast-running solution? Objective: Take the value of X at each timepoint and calculate the corresponding value of Y. Leading 0's and all 1's for X are assigned to Y; otherwise Y is incremented by the number of 0's adjacent to the last 1. The frequency and

Dear all R users, I want to realize 800 000 ANOVAS and to store Sum of Squares of the effects. Here is an extract of my table data Product attribute subject rep t1 t2 t3 … t101 P1 A1 S1 R1 1 0 0 … 1 I want to realize 1 ANOVA per timepoint and per attribute, there are 101 timepoints and 8 attributes so I want to realize 808 ANOVAS. This will be an ANOVA with two factors : Here is one example:

I have the following dataset: 96 plots 12 varieties 2 time points The experiment is arranged as follows: A single plot has two varieties tested on it. With respect to time points, plots come in 3 kinds: (1) varietyA, timepoint#1 vs. variety B, timepoint#1 (2) varietyA timepoint #2 vs. varietyB timepoint #2 (3) varietyA timepoint #1 vs. variety A timepoint#2 - there are 36 of each kind

I get the error undefined symbol: Rf_rownamesgets when I try to load my package, which include C++ code that calls that function. This is particularly strange since the code also calls Rf_classgets, and it loaded OK with just that. Can anyone tell me what's going on? For the record, I worked around this with the general purpose attribute setting commands and R_RowNamesSymbol. I

1) I have the following data situation: 96 plots 12 varieties 2 time points 2 technical treatments the experiment is arranged as follows: a single plot has two varieties tested on it. if variety A on plot #1 has treatment T1 applied to it, then variety B on plot #1 has treatment T2 applied to it. across the whole experiment variety A is exposed to treatment T1 the same number of times as

Hello, helpeRs, I am attempting to reshape (either base R or package reshape) multiple .csv spreadsheets from a very unfortunate wide format to long format. ?Each spreadsheet looks something like this, after being read in to R: toy <- data.frame(year = rep(2007:2008,each = 20), month = rep(1:5,each = 4, length = 40), day = rep(1:2,each = 2,length = 40), hhmm = rep(1100:1101,length = 40),

Hello, I am having some trouble with the 'censoring-adjusted C-index' by Uno et al, in the package survAUC. The relevant function is UnoC. The question has to do with what happens when I specify a time point t for the upper limit of the time range under consideration (we want to avoid using the right-end tail of the KM curve). Copying from the example in the help file: TR <-

Hi, I'm a database admin for a database which manage chromatographic results of products during stability studies. I use R for the reporting of the results in MS Word through R2wd. But now I think I need your help: suppose we have the following data frame: ID rrt Mnd Result 1 0.45 0 0.10 1 0.48 0 0.30 1 1.24 0 0.50 2 0.45 3 0.20 2 0.48 3 0.60 2 1.22 3 0.40 3

OK... i've come across a problem trying to get the granule pos of the start of the page... it's not so crucial with single stream ogg files... but now that i have theora+vorbis in a file, i'm finding that when i seek to a position, i have no way to determine the relative offsets of the different streams at the new seek point and hence the av is out of sync. So given a page, is it

Dear All, I am doing experiments in live plant tissue using a laser confocal microscope. The method is called "fluorescence recovery after photo-bleaching" (FRAP) and here follows a short summary: 1. Record/ measure fluorescence intensity in a defined, round region of interest (ROI, in this case a small spot) to determine the initial intensity value before the bleaching. This

All, How does one extract the level-1 variance from a model fit via lmer()? In the code below the level-2 variance component may be obtained via subscripting, but what about the level-1 variance, viz., the 3.215072 term? (actually this term squared) Didn't see anything in the archives on this. Cheers, David > fm <- lmer( dv ~ time.num*drug + (1 | Patient.new), data=dat.new )