Displaying 20 results from an estimated 30000 matches similar to: "(no subject)"
2005 Oct 07
3
Converting PROC NLMIXED code to NLME
Hi,
I am trying to convert the following NLMIXED code to NLME, but am
running into problems concerning 'Singularity in backsolve'. As I am new
to R/S-Plus, I thought I may be missing something in the NLME code.
NLMIXED
***********
proc nlmixed data=kidney.kidney;
parms delta=0.03 gamma=1.1 b1=-0.003 b2=-1.2 b3=0.09 b4=0.35 b5=-1.43
varu=0.5;
eta=b1*age+b2*sex+b3*gn+b4*an+b5*pkn+u;
2009 May 02
1
value labes Stata vs factors
Dear Sir/Madam,
I converted my Stata Rgenmetvl.dta file with read.dta succesfully in R's
Rgenmetvl.Rdata. However, factors give problem in certain calculations,
e.g.:
> mean(Rgenmetvl$sex)
[1] NA
Warning message:
In mean.default(Rgenmetvl$sex) :
argument is not numeric or logical: returning NA
What can I do?
In addition to means, summary(Rgenmetvl$sex) works perfectly.
Best regards,
2006 May 20
1
ANCOVA, Ops.factor, singular fit???
I'm trying to perform ANCOVAs in R 1.14, on a Mac OS X, but I can't figure out
what I am doing wrong. Essentially, I'm testing whether a number of
quantitative dental measurements (the response variables in each ANCOVA) show
sexual dimorphism (the sexes are the groups) independently of the animal's size
(the concomitant variable). I have attached a 13-column matrix as a data
2008 Jan 15
1
Anova for stratified Cox regression
Dear List,
I have tried a stratified Cox Regression, it is working fine, except for
the "Anova"-Tests:
Here the commands (should work out of the box):
library(survival)
d = colon[colon$etype==2, ]
m = coxph(Surv(time, status) ~ strata(sex) + rx, data=d)
summary(m)
# Printout ok
anova(m, test='Chisq')
This is the output of the anova command:
> Analysis of Deviance Table
2008 Jan 08
1
Problem in anova with coxph object
Dear R users,
I noticed a problem in the anova command when applied on
a single coxph object if there are missing observations in
the data:
This example code was run on R-2.6.1:
> library(survival)
> data(colon)
> colondeath = colon[colon$etype==2, ]
> m = coxph(Surv(time, status) ~ rx + sex + age + perfor, data=colondeath)
> m
Call:
coxph(formula = Surv(time, status) ~ rx +
2008 Jan 07
1
xtable (PR#10553)
Full_Name: Soren Feodor Nielsen
Version: 2.5.0
OS: linux-gnu
Submission from: (NULL) (130.225.103.21)
The print-out of xtable in the following example is wrong; instead of yielding
the correct ci's for the second model it repeats the ci's from the first model.
require(xtable)
require(MASS)
data(cats)
b1<-lm(Hwt~Sex,cats)
b2<-lm(Hwt~Sex+Bwt,cats)
2008 Apr 28
2
F values from a Repeated Measures aov
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
2007 Dec 07
1
paradox about the degree of freedom in a logistic regression model
Dear all:
"predict.glm" provides an example to perform logistic regression when the
response variable is a tow-columned matrix. I find some paradox about the
degree of freedom .
> summary(budworm.lg)
Call:
glm(formula = SF ~ sex * ldose, family = binomial)
Deviance Residuals:
Min 1Q Median 3Q Max
-1.39849 -0.32094 -0.07592 0.38220 1.10375
2006 Oct 30
1
help_aov
Hi,
I am trying to run an analysis of variance using R.
in my data table "x" is a continuous variable lengthof 200 and "p" is a
categorical variable also of length 200 and p is anyone of three categories
1,2 or ,3.
if I run
summary(aov(x~p,data=test))
I get
Response: x
Df Sum Sq Mean Sq F value Pr(>F)
p 1 3174.7 3174.7 42.749 5.175e-10 ***
2006 Sep 03
2
Running cox models
Hi,
I'm reading van Belle et al "Biostatistics" and trying to run a cox test using
a dataset from:
http://faculty.washington.edu/~heagerty/Books/Biostatistics/chapter16.html
(Primary Biliary Cirrhosis data link at top of the page),
I'm using the following code:
--------------- start of code
library(survival)
liver <-
2008 Oct 09
1
Error when reading a SAS transport file
Dear All,
I get the following error when using either SASxport or Hmisc to read an
.xpt file:
> w <- read.xport("D:/consult/Trophos/dnp/base/TRO_ds_20081006.xpt")
Erreur dans factor(x, f$value, f$label) :
invalid labels; length 15 should be 1 or 14
> z<- sasxport.get("D:/consult/Trophos/dnp/base/TRO_ds_20081006.xpt")
Erreur dans factor(x, f$value, f$label) :
2006 Oct 05
4
glm with nesting
I just had a manuscript returned with the biggest problem being the
analysis. Instead of using principal components in a regression I've
been asked to analyze a few variables separately. So that's what I'm
doing.
I pulled a feather from young birds and we quantified certain aspects of
the color of those feathers. Since I often have more than one sample
from a nest, I thought I
2007 Jun 18
1
how to obtain the OR and 95%CI with 1 SD change of a continue variable
Dear all,
How to obtain the odds ratio (OR) and 95% confidence interval (CI) with
1 standard deviation (SD) change of a continuous variable in logistic
regression?
for example, to investigate the risk of obesity for stroke. I choose the
happening of stroke (positive) as the dependent variable, and waist
circumference as an independent variable. Then I wanna to obtain the OR
and 95% CI with
2007 Dec 06
1
Building package - tab delimited example data issue
Hello,
I'm trying to integrate example data in the shape of a tab delimited ASCII
file into my package and therefore dropped it into the data subdirectory.
The build works out just fine, but when I attempt to install I get:
** building package indices ...
Error in scan(file, what, nmax, sep, dec, quote, skip, nlines,
na.strings, :
line 1 did not have 500 elements
Calls: <Anonymous>
2010 Sep 10
3
(no subject)
Hello,
I'm trying to do bar plot where 'sex' will be the category axis and
'occupation' will represent the bars and the clusters will represent
the mean 'income'.
sex occupation income
1 female j 12
2 male b 34
3 male j 22
4 female j 54
5 male b 33
6
2007 Aug 22
4
within-subject factors in lme
I don't think, this has been answered:
> I'm trying to run a 3-way within-subject anova in lme with 3
> fixed factors (Trust, Sex, and Freq), but get stuck with handling
> the random effects. As I want to include all the possible random
> effects in the model, it would be something more or less
> equivalent to using aov
>
> > fit.aov <- aov(Beta ~
>
2008 Sep 14
2
Help please! How to code a mixed-model with 2 within-subject factors using lme or lmer?
Hello,
I'm using aov() to analyse changes in brain volume between males and
females. For every subject (there are 331 in total) I have 8 volume
measurements (4 different brain lobes and 2 different tissues
(grey/white matter)). The data looks like this:
Subject Sex Lobe Tissue Volume
subect1 1 F g 262374
subect1 1 F w 173758
subect1 1 O g 67155
subect1 1 O w 30067
subect1 1 P g 117981
2006 Mar 24
4
How to capture t-score and p-values from t.test
When I do t.test on two distributions (see example below), it outputs
numerous data about the t.test.
What I'd like to do is individually capture some of this data and assign
it to other variables.
However, I am unable to find anything in the help section.
In the example below, the t value is -4.0441 and the p-value is 0.006771
How can I assign these values to two variables, let's
2007 Nov 28
2
fit linear regression with multiple predictor and constrained intercept
Hi group,
I have this type of data
x(predictor), y(response), factor (grouping x into many groups, with 6-20
obs/group)
I want to fit a linear regression with one common intercept. 'factor'
should only modify the slopes, not the intercept. The intercept is expected
to be >0.
If I use
y~ x + factor, I get a different intercept for each factor level, but one
slope only
if I use
y~ x *
2010 Feb 05
2
(Another) Bates fortune?
I vote to 'fortunize' Doug Bates on
Hierarchical data sets: which software to use?
"The widespread use of spreadsheets or SPSS data sets or SAS data sets
which encourage the "single table with a gargantuan number of columns,
most of which are missing data in most cases" approach to organization
of longitudinal data is regrettable."