Displaying 20 results from an estimated 10000 matches similar to: "Replacing sets of rows in matrix within a loop"
2012 Jun 18
6
Trying to speed up an if/else statement in simulations
Dear R-help,
I am trying to write a function to simulate datasets of size n which contain
two time-to-event outcome variables with associated 'Event'/'Censored'
indicator variables (flag1 and flag2 respectively). One of these indicator
variables needs to be dependent on the other, so I am creating the first and
trying to use this to create the second using an if/else statement.
2002 Dec 20
5
Getting graphs into LaTeX
Hello ALL:
I ran with success the following commands in R getting a file saved
------------------------------------------------------------------------------------
postscript()
postscript('~/data/st202/2003/lecture00/lecture00-graph-01.eps',
horizontal = FALSE, height = 6, pointsize = 10)
hist(trial.outcome.5, breaks = 5,
main = '1000 Replications of 5 Trials of a
2010 Sep 23
2
Error: attempt to apply non-function
This code worked fine for me, then did some cleaning up of formatting using ESS (Emacs) and now I get this error, no idea what is causing it, all the brackets/parentheses seem to be balanced. What have I done wrong?
Thanks
Jim
p0.trial01 <- 0.25
TruOR01 <- 0.80
num.patients.01 <- 50
num.trials.01 <- 5
LOR01.het.in <- 0.00
num.sims <- 1
simLOR01 <-
2010 Jul 02
1
metafor and meta-analysis at arm-level
Hi,
I have been looking for an R package which allowed to do meta-analysis
(both pairwise and network/mixed-treatment) at arm-level rather than at
trial-level, the latter being the common way in which meta-analysis is
done.
By arm-level meta-analysis I mean one that accounts for data provided at
the level of the individual arms of each trial and that does not simply
derive the difference between
2006 Mar 03
1
Help with lme and correlated residuals
Dear R - Users
I have some problems fitting a linear mixed effects model using the lme function (nlme library). A sample data is as shown at the bottom of this mail. I fit my linear mixed model
using the following R code:
bmr <-lme (outcome~ -1 + as.factor(endpoint)+ as.factor(endpoint):trt, data=datt,
random=~-1 + as.factor(endpoint) + as.factor(endpoint):trt|as.factor(Trial),
2006 Mar 07
1
lme and gls : accessing values from correlation structure and variance functions
Dear R-users
I am relatively new to R, i hope my many novice questions are welcome.
I have problems accessing some objects (specifically the random effects, correlation structure and variance function) from an object of class gls and lme.
I used the following models:
yah <- gls (outcome~ -1 + as.factor(Trial):as.factor(endpoint)+
2009 Mar 10
1
Nesting order for mixed models
Hello,
I am confused about the order of nesting in mixed models using functions
like aov(), lme(), lmer().
I have the following data:
n subjects in either condition A or B
each subject tested at each of 3 numerical values ("distance" =
40,50,60), repeated 4 times for each of the 3 numerical values ("trial"
= 1,2,3,4)
Variable summary:
Condition: 2 level factor
Distance:
2009 Apr 10
1
How to handle tabular form data in lmer without expanding the data into binary outcome form?
Dear R-gurus:
I have a question about lmer.
Basically, I have a dataset, in which each observation records number of
trials (N) and number of events (Y) given a covariate combination(X) and
group id (grp_id).
So, my dataset is in tabular form. (in case my explanation of tabular form
is unclear,
please see the link:
2006 Feb 03
5
pbinom with size argument 0 (PR#8560)
Full_Name: Uffe H?gsbro Thygesen
Version: 2.2.0
OS: linux
Submission from: (NULL) (130.226.135.250)
Hello all.
pbinom(q=0,size=0,prob=0.5)
returns the value NaN. I had expected the result 1. In fact any value for q
seems to give an NaN. Note that
dbinom(x=0,size=0,prob=0.5)
returns the value 1.
Cheers,
Uffe
2006 Nov 09
2
Meta-regression with lmer() ? If so, how ?
Dear List,
I am (again) looking at meta-regression as a way to refine meta-analytic
results. What I want to do is to assess the impact of some fixed factors
on the results of a meta-analysis. Some of them may be crossed with the
main factor of the meta-analysis (e. g. clinical presentation of a
disease, defining subgroups in each of the studies under analysis), some
of them may be a grouping
2007 May 31
1
Conditional logistic regression for "events/trials" format
Dear R users,
I have a large individual-level dataset (~700,000 records) which I am
performing a conditional logistic regression on. Key variables include
the dichotomous outcome, dichotomous exposure, and the stratum to which
each person belongs.
Using this individual-level dataset I can successfully use clogit to
create the model I want. However reading this large .csv file into R and
running
2010 Sep 20
2
OT: Is randomization for targeted cancer therapies ethical?
Hi Folks:
**Off Topic**
Those interested in clinical trials may find the following of interest:
http://www.nytimes.com/2010/09/19/health/research/19trial.html
It concerns the ethicality of randomizing those with life-threatening
disease to relatively ineffective SOC when new "biologically targeted"
therapies "appear" to be more effective. While the context may be new,
the
2011 May 13
2
L'abbe plot
I cannot seem to get a L'abbe plot to work on R. I do not understand what
the X coordinates, or alternatively an object of class metabin, is
supposed to mean. What is a class of metabin?
Institute of Behavioral Genetics
University of Colorado, Boulder
Whitney.Melroy at Colorado.EDU
2008 Sep 25
2
ggplot, qplot in loop
Dear List,
yes, me again trying to work with qplot ;-)
I would like to make several single plots within a loop, like this
(simplified and so on...):
trials <- c("A","B","C")
mycolours <- ("wheat","darkolivegreen","lightgreen",
2018 Jan 07
1
Defining interaction in random effects in lme4
Dear everybody!
My fixed-effects-only model looks like this: glmer(Accuracy ~ C.RT*Group,
data = da)
C.RT is the reaction time variable, and Group is a categorical variable
with 0 and 1 as values. I would like to specify that main intercept, Group
intercept, C.RT slope and C.RT*Group slope vary across subjects and trials.
All subjects have values in Group = 0 and in Group = 1. Trials are nested
2013 Feb 25
1
creating variable that codes for the match/mismatch between two other variables
Dear all,
I have got two vectors coding for a stimulus presented in the current trial (mydat$Stimulus) and a prediction in the same trial (mydat$Prediciton), respectively.
By applying an if-conditional I want to create a new vector that indicates if there is a match between both vectors in the same trial. That is, if the prediction equals the stimulus.
When I pick out some trials randomly, I get
2003 Jan 29
3
Analyzing an unbalanced AB/BA cross-over design
I am looking for help to analyze an unbalanced AB/BA cross-over design by
requesting the type III SS !
# Example 3.1 from S. Senn (1993). Cross-over Trials in Clinical
Research
outcome<-c(310,310,370,410,250,380,330,270,260,300,390,210,350,365,370,310,380,290,260,90,385,400,410,320,340,220)
subject<-as.factor(c(1,4,6,7,10,11,14,1,4,6,7,10,11,14,2,3,5,9,12,13,2,3,5,9,12,13))
2003 Feb 26
2
na.action in model.tables and TukeyHSD
Hello everybody!
I use R 1.6.2 in Windows, and have a problem controlling the na.action.
In a dataset with twelve trials, one of the trials lack any readings of the variable "STS.SH" (standing power at harvest)
Fitting an aov() object with the call:
led1t7sts.aov <- aov(STS.SH ~ Trial/Block + Treatment + Treatment:Trial, data = led1t7, na.action=na.exclude)
seems to work as it
2007 Mar 30
1
faster computation of cumulative multinomial distribution
Dear list members,
I have a series of /unequal/ probabilities [p1,p2,...,pk], describing
mutually exclusive events, and a "remainder" class with a probability
p0=1-p1-p2-....-pk, and need to calculate, for a given number of trials
t>=k, the combined probability that each of the classes 1...k contains
at least 1 "event" (the remainder class may be empty).
To me this reaks
2011 Apr 22
1
Survival analysis: same subject with multiple treatments and experience multiple events
Hi there,
I need some help to figure out what is the proper model in survival analysis
for my data.
Subjects were randomized to 3 treatments in trial 1, some of them experience
the event during the trial;
After period of time those subjects were randomized to 3 treatments again in
trial 2, but different from what they got in 1st trial, some of them
experience the event during the 2nd trial (I