similar to: R-alpha: frame tools

Displaying 20 results from an estimated 5000 matches similar to: "R-alpha: frame tools"

2007 May 01
7
logrank test
how do l programme the logrank test. l am trying to compare 2 survival curves --------------------------------- [[alternative HTML version deleted]]
2007 May 30
2
control axis
I have an outlier that I would still like to display, but would prefer to shorten the axis. For example, display 0% - 40%, and 90% - 100%. Is this possible? I am using an xyplot. Thanks Murray -- Murray Pung Statistician, Datapharm Australia Pty Ltd 0404 273 283 [[alternative HTML version deleted]]
2009 Jan 20
1
generalizing expand.table: table -> data.frame
In http://tolstoy.newcastle.edu.au/R/e2/help/06/10/3064.html a method was given for converting a frequency table to an expanded data frame representing each observation as a set of factors. A slightly modified version was later included in the NCStats package, only on http://rforge.net/ (and it has too many dependencies to be useful). I've tried to make it more general, allowing an input
2006 Jan 03
1
p-value of Logrank-Test
Hello! I want to compare two Kaplan-Meier-Curves by using the Logrank-Test: logrank(Surv(time[b], status[b]) ~ group[b]) This way I only get the value of the test-statistic, but not the p-value. Does anybody know how I can get the p-value? Thanks in advance! Verena Hoffmann
2013 Sep 13
1
Creating dummy vars with contrasts - why does the returned identity matrix contain all levels (and not n-1 levels) ?
Hello, I have a problem with creating an identity matrix for glmnet by using the contrasts function. I have a factor with 4 levels. When I create dummy variables I think there should be n-1 variables (in this case 3) - so that the contrasts would be against the baseline level. This is also what is written in the help file for 'contrasts'. The problem is that the function
1997 May 20
1
R-alpha: planned update of ctest
I am contemplating improving my ctest package as follows: * Add exact p,q,r,s functions for the Wilcoxon distribution, and change the test accordingly (make `exact' work). * Make Fisher's test work for tables larger than 2 by 2. * Perhaps add an exact unconditional test for 2 by 2 tables? * Perhaps add something on estimating/testing relative risk and odds? As clearly I'd like to
2011 Nov 20
1
Cox proportional hazards confidence intervals
I am calculating cox propotional hazards models with the coxph function from the survival package. My data relates to failure of various types of endovascular interventions. I can successfully obtain the LR, Wald, and Score test p-values from the coxph.object, as well as the hazard ratio as follows: formula.obj = Surv(days, status) ~ type coxph.model = coxph(formula.obj, df) fit =
2007 May 17
2
How to analyse simple study: Placebo-controlled (2 groups) repeated measurements (ANOVA, ANCOA???)
Hallo! I have two groups (placebo/verum), every subject is measured at 5 times, the first time t0 is the baseline measurement, t1 to t4 are the measurements after applying the medication (placebo or verum). The question is, if there is a significant difference in the two groups and how large the differnce is (95% confidence intervals). Let me give sample data # Data
2009 Feb 27
2
Adjusting confidence intervals for paired t-tests of multiple endpoints
Dear R-users, In a randomized placebo-controlled within-subject design, subjects recieved a psycho-active drug and placebo. Subjects filled out a questionnaire containing 15 scales on four different time points after drug administration. In order to detect drug effects on each time point, I compared scale values between placebo and drug for all time conditions and scales, which sums up to
2008 Mar 14
2
problems creating data frames
I am having two problems creating data frames that I have solutions, but they really seem like kludges and I assume I just don't understand the proper R way of doing things. The first situation is I have an set of uneven data vectors. When I try to use them to create a data frame I would like the bottoms of them padded with NAs, without explicitly specifying that. When I do: anxiety.data =
2011 Mar 01
1
glht() used with coxph()
Hi, I am experimenting with using glht() from multcomp package together with coxph(), and glad to find that glht() can work on coph object, for example: > (fit<-coxph(Surv(stop, status>0)~treatment,bladder1)) coxph(formula = Surv(stop, status > 0) ~ treatment, data = bladder1) coef exp(coef) se(coef) z p treatmentpyridoxine -0.063 0.939 0.161
2012 Oct 23
5
List of multidimensional arrays
Dear all, I am trying to create a list, where each list element is a vector of different length arrays that contain 2by2 matrices. To be more specific there are 11 treatments that are compared with placebo (we have 11 comparisons) and each comparison is studied by a different number of trials and each trial has a different number of missing participants in both arms. The length of the list is
2004 Aug 27
3
reorder [stats] and reorder.factor [lattice]
It was recently pointed out on the lists that the S-PLUS Trellis suite has a function called reorder.factor that's useful in getting useful ordering of factors for graphs. I happily went ahead and implemented it, but it turns out that R (not S-PLUS) has a generic called reorder (with a method for "dendrogram"). Naturally, this causes R to think I'm defining a method for
2010 Jul 22
1
gam() and contrast
Dear All, I met problems when doing contrast and now really need some help in the model below: Fit=gam(y~treat+SEQUENCE+PERIOD+SEX+s(x),data=dat, random=list(SUBJID=~1),correlation=corAR1(form=~1|SUBJID)) And error message keeps coming out when I want to compare the differences between treatments: Diff=contrast(Fit, list(treat=treatment[-placebo.pos]),list(treat="Placebo"),
2007 May 14
1
Nicely formatted summary table with mean, standard deviation or number and proportion
Dear all, The incredibly useful Hmisc package provides a method to generate summary tables that can be typeset in latex. The Alzola and Harrell book "An introduction to S and the Hmisc and Design libraries" provides an example that generates mean and quartiles for continuous variables, and numbers and percentages for count variables: summary() with method = 'reverse'. I
2009 Feb 02
2
parsing problem
Hi all, I am trying to parse a vector for caliculating minimum in that vector the vector having values like 1 Kontrolle 2 Placebo 3 125mg/kg 4 250mg/kg 5 500mg/kg 6 1000mg/kg hear i tries for comverting it into numeric with using "as.numaric()" function but i got values like 5 6 2 3 4 1 it gives 1000mg/kg is the least one but i have
2007 May 07
2
computing logrank statistic/test
hie how do you compute the logrank test using R what commands do you use my data looks something like just an example treatmentgrp strata censoringTime survivalTime censoring act.surv.time [1,] 2 2 42.89005 1847.3358 1 42.89005 [2,] 1 1 74.40379 440.3467 1 74.40379 [3,] 2 2
2007 Sep 27
1
windows device transparency issue
I read in a thread in r-help today that the windows device in 2.6 supports transparency, so I tried an example and had some issues. The density plots should be filled with transparent color in the following example (similar to the points), however the color is "fully" transparent. This works in the Cairo device, but not in the windows device. Thanks, --Matt Matt Austin
2008 Jul 02
1
auto.key in xyplot in conjunction with panel.text
All, I can't seem to get auto.key to work properly in an xyplot that is employing panel.text. Specifically, I often change the default grouping colors then use auto.key accordingly, but for some reason the same functionality isn't working for this different type of plot. Any help much appreciated. Cheers, David library("lattice") dat = data.frame( Y = c(rnorm(18,1),
2006 Sep 26
2
treatment effect at specific time point within mixed effects model
All, The code below is for a pseudo dataset of repeated measures on patients where there is also a treatment factor called "drug". Time is treated as categorical. What code is necessary to test for a treatment effect at a single time point, e.g., time = 3? Does the answer matter if the design is a crossover design, i.e, each patient received drug and placebo? Finally, what would