Is it correct that one does not need to escape special characters such as
* (are these
properly called metacharacters) inside []. If so, what is the logic to this?
mytest - he*llo
sub([*],,mytest)
sub(\\*,,mytest)
[] is easier to read for me than \\. Is this what people tend to use?
Thanks.
Hi Jan and Simon,
If possible, could you attach the diagnostic plots. I would be curious to
see them.
Thanks,
Juliet
On Fri, Apr 19, 2013 at 4:39 AM, jholstei jan.holst...@awi.de wrote:
Simon,
that was very instructivevery special thanks to you.
I already noticed that the model was bad,
All,
Can someone describe what
x[] - lapply(x, as.numeric)
I see that it is putting the list elements into a data frame. The
results for lapply are a list, so how does this become
a data frame.
Thanks,
Juliet
On Mon, Dec 3, 2012 at 5:49 PM, Fisher Dennis fis...@plessthan.com
:
Hello,
Because x[] keeps the dimensions, unlike just x.
Hope this helps,
Rui Barradas
Em 06-12-2012 16:24, Juliet Hannah escreveu:
All,
Can someone describe what
x[] - lapply(x, as.numeric)
I see that it is putting the list elements into a data frame. The
results for lapply
See the post by Frank Harrell at:
http://groups.google.com/group/medstats/browse_thread/thread/cbff7871179e9508?pli=1
or google
regrouping to satisfy proportional odds
On Tue, May 1, 2012 at 2:14 AM, 80past2 benny...@gmail.com wrote:
Hi everyone, I'm a bit new here (and new to R), and I was
Max and List,
Could you advise me if I am using the proper caret syntax to carry out
leave-one-out cross validation. In the example below, I use example
data from the rda package. I use caret to tune over a grid and select
an optimal value. I think I am then using the optimal selection for
, but the
scaling is also off, which suggests a bigger mistake.
Thanks for your help.
Juliet Hannah
library(ElemStatLearn)
library(glmnet)
data(prostate)
# training data
data.train - prostate[prostate$train,]
y - data.train$lpsa
# isolate predictors
data.train - as.matrix(data.train[,-c(9,10
Oops. Coefficients are returned on the scale of the original data.
testX - cbind(1,data.test)
yhat2 - testX %*% beta
# works
plot(yhat2,yhat_enet)
On Wed, Mar 21, 2012 at 2:35 PM, Juliet Hannah juliet.han...@gmail.com wrote:
All,
For my understanding, I wanted to see if I can get glmnet
For quantile normalization check out
normalize.quantiles in the Biocondcutor preProcess package. Also,
there is a Bioconductor mailing list for future where these topics
are discussed.
http://svitsrv25.epfl.ch/R-doc/library/preprocessCore/html/normalize.quantiles.html
On Sat, Jan 21, 2012 at
You may find the following discussion helpful.
http://comments.gmane.org/gmane.science.biology.informatics.conductor/37388
On Sun, Dec 11, 2011 at 8:08 AM, ali_protocol
mohammadianalimohammad...@gmail.com wrote:
Dear all,
Is there anyway too generate MA plot for 2 qPCR assays (an array of 2x
I am calculating the mean of each column grouped by the variable 'id'.
I do this using aggregate, data.table, and plyr. My aggregate results
do not match the other two, and I am trying to figure out what is
incorrect with my syntax. Any suggestions? Thanks.
Here is the data.
myData -
In the solution below, what is the advantage of using 0L.
M0 - read.csv(M1.csv, nrows = 1)[0L, ]
Thanks!
2011/11/8 Gabor Grothendieck ggrothendi...@gmail.com:
2011/11/8 Sergio René Araujo Enciso araujo.enc...@gmail.com:
Dear all:
I have two larges files with 2000 columns. For each file I
Search: mcmcglmm heritability to see some discussions using the
mcmcglmm package. This package is discussed often
on the mixed model list. You can also use the kinship package. It will
take some time to get familiar with R. Work through
a few of the examples for variance component models, and then
Note that exprs returns a matrix, so we can manipulate that just as we
would for any other type of matrix. There is also a Bioconductor
mailing list, which may be helpful.
On Thu, Oct 6, 2011 at 4:56 AM, Clayton K Collings ccoll...@purdue.edu wrote:
Hello R people,
dim(exprs(estrogenrma)
I
Maybe some of the comments in this post may be informative to you:
http://r.789695.n4.nabble.com/improve-formatting-of-HTML-table-td3736299.html
On Wed, Sep 28, 2011 at 6:21 AM, David Scott d.sc...@auckland.ac.nz wrote:
I have been playing around with producing tables using xtable and the type
I am using the example in this post:
https://stat.ethz.ch/pipermail/r-help/2010-October/257204.html
# create a file
write.table(iris,iris.csv,row.names=FALSE,sep=,,quote=FALSE)
# this does not work
# has the syntax changed or is there a mistake in my usage?
# the line from the post above is:
Workshop
was at the beginning.
With this, my attempts at package creation worked.
On Thu, Jun 30, 2011 at 12:51 PM, Juliet Hannah juliet.han...@gmail.com wrote:
I am trying to build a package using windows xp. Here is the error I am
getting:
R CMD build myfunctions
* checking for file
List,
Consider the following data.
gender mygroup id
1 F A 1
2 F B 2
3 F B 2
4 F B 2
5 F C 2
6 F C 2
7 F C 2
8 F D 2
9 F D 2
10 F D 2
11 F D 2
12 F
I have a data set with about 6 million rows and 50 columns. It is a
mixture of dates, factors, and numerics.
What I am trying to accomplish can be seen with the following
simplified data, which is given as dput output below.
head(myData)
mydate gender mygroup id
1 2012-03-25 F
= length(rle(mygroup)$lengths) - 1), by = 'id'] # ditto
HTH,
Dennis
On Wed, Aug 24, 2011 at 9:48 AM, Juliet Hannah juliet.han...@gmail.com
wrote:
I have a data set with about 6 million rows and 50 columns. It is a
mixture of dates, factors, and numerics.
What I am trying to accomplish
Thanks to Duncan Mackay and Dennis Murphy for help.
The following solution seems to give me what I need.
library(memisc)
toLatex(ftable(cyl ~ am,data=mtcars))
For this to work, we have to use:
\documentclass{article}
\usepackage{booktabs}
\usepackage{dcolumn}
\begin{document}
at the beginning
Thanks for the suggestion, Duncan.
However, I was trying to maintain the contingency
table/cross-classification structure of the original table.
My use of xtable on this table, maintains the structure I want, but
the labels for the rownames and colum names is lost.
On Tue, Aug 16, 2011 at
In R, the output of xtabs displays the names of the dimnames. In the
example below, these are change_diet and mydiet. Is there a way to
have xtable incorporate these names directly into the latex output.
Thanks for your help.
table2 - structure(c(26, 0, 40, 0, 10, 0, 188, 0, 281, 0), .Dim =
I am trying to improve the look of an HTML table for a report (that
needs to be pasted into Word).
Here is an example.
table2 - structure(c(26L, 0L, 40L, 0L, 10L, 0L, 0L, 188L, 0L, 281L, 0L,
0L, 0L, 0L, 0L, 0L, 0L, 4L), .Dim = c(6L, 3L), .Dimnames = structure(list(
myvar = c(Don't know,
...@comcast.net wrote:
On Jul 12, 2011, at 4:37 PM, Juliet Hannah wrote:
I have a file in stata format, which I have read in, and I am trying
to create a text file. I have exported the data using various
delimiters, but I'm unable to read it back in. I originally read in
the file
I have a file in stata format, which I have read in, and I am trying
to create a text file. I have exported the data using various
delimiters, but I'm unable to read it back in. I originally read in
the file with:
library(foreign)
myData - read.dta(mydata.dta)
I then exported it with write.table
See if the following thread
http://www.mail-archive.com/r-help@r-project.org/msg85070.html
and the paper cited in it are helpful. Terry Therneau provides code
for a Deming regression.
On Thu, Jul 7, 2011 at 12:58 PM, devon woodcomb d.woodco...@gmail.com wrote:
Hi,
I have a dataset which
I am trying to build a package using windows xp. Here is the error I am getting:
R CMD build myfunctions
* checking for file 'myfunctions/DESCRIPTION' ... OK
* preparing 'myfunctions':
* checking DESCRIPTION meta-information ... OK
* checking for LF line-endings in source and make files
*
I have a data frame in which missing values exist, and I need to
recode the string missing to a missing value. For the example, let's
assume I cannot do this while reading it in. Even though this has been
discussed extensively, I'm still a little confused about when to index
with which and when to
# Let's say your expression data is in a matrix
# named expression in which the rows are genes
# and the columns are samples
myvars - apply(expression,1, var,na.rm=TRUE)
myvars - sort(myvars,decreasing=TRUE)
myvars - myvars[1:200]
expression - expression[names(myvars),]
dim(expression)
Also
The 'findCorrelation' function in the caret package may be helpful.
On Tue, Apr 19, 2011 at 3:10 PM, Rita Carreira ritacarre...@hotmail.com wrote:
Hello R Users!
I have a data frame that has many variables, some with missing observations,
and some that are correlated with each other. I
As you mentioned, the deviance does not always reduce to:
D = -2(loglikelihood(model))
It does for ungrouped data, such as for binary logistic regression. So
let's stick with the original definition.
In this case, we need the log-likelihood for the saturated model.
x = rnorm(10)
y =
Maybe the pedigree is not set up correctly. If this is the case, the
kinship matrix will not be constructed correctly. I see that in this
example,
the diagonal terms differ.
diag(kmat)
lmekin runs fine for me, and I can extract p-values with:
lmekinfit - lmekin(...)
pval -
Use exprs on the output from RMA (or another method you like)
library(affy)
myData -ReadAffy()
myRMA - rma(myData)
e = exprs(myRMA)
Also, check out the Bioconductor mailing list where
Bioconductor-related topics are discussed.
On Fri, Apr 1, 2011 at 9:54 AM, Landes, Ezekiel
If you can work with a different penalty check out the lrm function
from the rms package, which uses
penalized likelihood to fit proportional odds.
2011/3/24 Jheng-Jhong Wang iiamba...@gmail.com:
Dear R-users,
I try to fit proportional odds ratio model with LASSO in
ordinal
Relatedness if often defined in terms of the kinship matrix. It may be
helpful to search for this. Several packages in R use this matrix
including the kinship package.
On Wed, Feb 16, 2011 at 3:14 PM, Val valkr...@gmail.com wrote:
Hi all,
I want to construct relatedness among individuals and
If you could provide a small example of an actual data set (using
dput), you may get some suggestions
specific to your goals.
Here are a few examples of boxplots. If these look along the lines of
what you are looking for, you may want to search
the ggplot2 mailing list for more examples.
GWAF uses the kinship package. The documentation is pretty good for
it, and I've used it successfully. It may be helpful to get that
working before trying automate some tasks using GWAF.
On Fri, Feb 4, 2011 at 2:20 PM, Jim Moon moo...@ohsu.edu wrote:
Hello, All,
GWAF 1.2
R.Version() is below.
It looks like the text didn't show assigning the results of factanal
to an object. Try:
pgdata-read.table(pgfull.txt,header=T)
names(pgdata)
pgd-pgdata[,1:54]
#missing line
model - factanal(pgd,8)
par(mfrow=c(2,2))
plot(loadings(model)[,1],loadings(model)[,2],pch=16,xlab=Factor
1,ylab=Factor 2)
Make sure your data is a matrix. There are many examples of expression heatmaps
available on the bioconductor list. After checking out these examples, I would
post to the bioconductor list if you are still having problems. Also
consider a small
example to get you a working heatpmap. You have to
Also check out the following post:
http://permalink.gmane.org/gmane.comp.lang.r.general/210897
On Sat, Nov 20, 2010 at 4:32 PM, casperyc caspe...@hotmail.co.uk wrote:
Hi,
I have count data
x2=rep(c(0:3),c(13,80,60,27))
x2
0 1 2 3
13 80 60 27
I want to graph to be ploted as
Check out ggplot2, specifically geom_bar and geom_text.
http://had.co.nz/ggplot2/
You have to get used to its syntax, which can take some time, but
after that it can make things a lot easier. Here is an example.
library(ggplot2)
df - data.frame(xvar = factor(c(1, 2)),
yvar = c(1, 5))
p -
I think the most common reason to see different parameter estimates
with ordinal regression is that programs set up
the model differently.
For example, check out
library(MASS)
?polr
We see polr uses:
logit P(Y = k | x) = zeta_k - eta
and notes that other software packages may use the opposite
See if rowttests is any faster.
library(genefilter)
?rowttests
You have to install Bioconductor. I've used this on large datasets,
but I haven't compared
timings.
On Mon, Sep 13, 2010 at 4:26 PM, Alexey Ush usha...@yahoo.com wrote:
Hello,
I have a question regarding how to speed up the
Hi Group,
I have a possibly naive question, but it seems like it fits into this
discussion.
I have observed that when researchers publish findings that are deemed
to be high-impact,
generous funding often follows.
R is used everywhere, and, of course, for many of these projects. So
my naive
Hi Group,
I have a data frame below. Within this data frame there are samples
(columns) that are measured more than once. Samples are indicated by
idx. So id1 is present in columns 1, 3, and 5. Not every id is
repeated. I would like to create a new data frame so that the repeated
ids are
I have downloaded a file that I don't know how to describe correctly.
It contains R code and Latex, and I should be able to reproduce an
analysis by running an R script in this folder.
There is a line in the R script:
junk - system(paste(/usr/texbin/pdflatex ,latexFiles[i1]),
, Juliet Hannah wrote:
I have downloaded a file that I don't know how to describe correctly.
It contains R code and Latex, and I should be able to reproduce an
analysis by running an R script in this folder.
There is a line in the R script:
junk- system(paste(/usr/texbin/pdflatex ,latexFiles[i1
Hi Jim,
I was trying to use your template without success. With the toy data
below, could
you explain how to use this template to change all bs to zs --
just as an exercise, reading
in 3 lines at a time. I need to use this strategy for a larger
problem, but I haven't
been able to get the basics
You may want to check out examples in lattice and ggplot2. Both of
these make plotting subsets much easier. I can't remember the lattice
syntax off the top of my head, but if you post some example data –
either by creating it or using dput – people will be able to help out
easier. Here is some
Here is some data (dput output below)
myData
id group
1 D599 A
2 002-0004 B
3 F01932
Hi Group,
I have a matrix, and I would like to replace numbers less than 0 by
the smallest minimum number. Below is an
small matrix, and the loop I used. I would like to get suggestions on
the R way to do this.
Thanks,
Juliet
# example data set
mymat - structure(c(-0.503183609420937,
, Juliet Hannah wrote:
Hi Group,
I have a matrix, and I would like to replace numbers less than 0 by
the smallest minimum number. Below is an
small matrix, and the loop I used. I would like to get suggestions on
the R way to do this.
Thanks,
Juliet
# example data set
mymat - structure(c
), by=list(V2) ]
Why you you need to reshape from long to wide ?
HTH,
Matthew
Juliet Hannah juliet.han...@gmail.com wrote in message
news:aanlktinyvgmrvdp0svc-fylgogn2ro0omnugqbxx_...@mail.gmail.com...
Hi Jim,
Thanks for responding. Here is the info I should have included before.
I should
.
This would be impossible on a 32-bit version of R.
On Mon, Jul 12, 2010 at 1:25 AM, Juliet Hannah juliet.han...@gmail.com
wrote:
I have a data set that has 4 columns and 53860858 rows. I was able to
read this into R with:
cc - rep(character,4)
myData -
read.table(myData.csv,header=FALSE
I have a data set that has 4 columns and 53860858 rows. I was able to
read this into R with:
cc - rep(character,4)
myData -
read.table(myData.csv,header=FALSE,skip=1,colClasses=cc,nrow=53860858,sep=,)
I need to reshape this data from long to wide. On a small data set the
following lines work.
You may find both of Alan Agresti's books on categorcial data analysis
useful. Try googling both books and then
search the word grouped within each book. Agresti refers to the
difference you describe as
grouped versus ungrouped data. The likelihoods differ and all
summaries based on the likelihood
I've used this package before, and it always gives me the message:
NOTE: THIS PACKAGE IS NOW OBSOLETE.
So I stopped using it. I just tried installing it and it gave me some
new errors (below). Maybe you should also post your sessionInfo().
library(genetics)
Loading required package: combinat
What is the meaning of \\1 here? Thanks.
desc - c(hsa-let-7a MIMAT062 Homo sapiens let-7a,hsa-let-7a*
MIMAT0004481 Homo sapiens let-7a*,hsa-let-7a-2* MIMAT0010195 Homo
sapiens let-7a-2*)
I'm missing something:
gsub( MIMA.*, \\1, desc)
[1] hsa-let-7ahsa-let-7a* hsa-let-7a-2*
gsub(
I am recoding some data. Many values that should be 1.5 are recorded
as 1-2. Some example data and my solution is below. I am curious about
better approaches or any other suggestions. Thanks!
# example input data
myData - read.table(textConnection(id, v1, v2, v3
a,1,2,3
b,1-2,,3-4
I started with the summarized data, and there are different ways to do
this. For this example, let there be four columns and a corresponding
sum of 1s.
library(ggplot2)
mydf - data.frame(colname = c(A,B,C,D),mycolsum=c(1:4))
p - ggplot(mydf,aes(x=colname,y=mycolsum))
p - p + geom_bar(stat =
Hi List,
I have a question about uninstalling and installing R on linux, which
I am new to.
sessionInfo()
R version 2.10.1 (2009-12-14)
x86_64-unknown-linux-gnu
locale:
[1] LC_CTYPE=en_US.UTF-8 LC_NUMERIC=C
[3] LC_TIME=en_US.UTF-8LC_COLLATE=en_US.UTF-8
[5] LC_MONETARY=C
This has not worked for me, meaning I can still use R, so instead I
removed the directory
rm -fR R-2.10.1
Is one method preferable to another. And what am I doing incorrectly
with make uninstall?
Don't know, probably not many are using it and it may be fairly untested.
If not many are
I installed R 2.11.0, and I don't think I can load the doBy package
now. Any suggestions?
library(doBy)
Loading required package: survival
Loading required package: splines
Error in loadNamespace(i[[1L]], c(lib.loc, .libPaths())) :
there is no package called 'Hmisc'
Error: package/namespace
I should have mentioned that I also tried:
install.packages(Hmisc)
Warning message:
In getDependencies(pkgs, dependencies, available, lib) :
package ‘Hmisc’ is not available
On Fri, Apr 23, 2010 at 3:15 PM, David Winsemius dwinsem...@comcast.net wrote:
On Apr 23, 2010, at 3:09 PM, Juliet
Some code to cut and paste would be helpful. The following may help out.
library(multtest)
# create some p-values
p - runif(100)
p - sort(p)
p_adj - mt.rawp2adjp(p, proc=BH, alpha = 0.05)
str(p_adj)
List of 4
$ adjp : num [1:100, 1:2] 0.0142 0.0174 0.0254 0.0258 0.0736 ...
..- attr(*,
I use rms, lme4, ggplot2 frequently (also lattice and MASS).
On Tue, Mar 2, 2010 at 3:13 PM, Ralf B ralf.bie...@gmail.com wrote:
Hi R-fans,
I would like put out a question to all R users on this list and hope
it will create some feedback and discussion.
1) What are your 3 most useful R
I didn't follow your question completely. But do a search for
intraclass correlation with nlme or lmer and see if those results
relate to the question you are asking. If so, I would
suggest following up on the mixed model list. I know you
wanted to avoid mixed models, but if I have understood
your
I just installed it, and it worked fine.
sessionInfo()
R version 2.10.1 (2009-12-14)
i386-pc-mingw32
locale:
[1] LC_COLLATE=English_United States.1252 LC_CTYPE=English_United
States.1252
[3] LC_MONETARY=English_United States.1252 LC_NUMERIC=C
[5] LC_TIME=English_United States.1252
attached
It would be easier with some example data. Make sure the data is represented by
factors and check the levels and relevel if needed. Something like:
df$day - factor(df$day, levels = c(30, 29, 20))
Also search the ggplot2 mailing list for factor and order. I think
similar questions
are asked often
Check out the book
Linear Mixed Models: A Practical Guide Using Statistical Software by
Brady West.
It sets up analyses, similar to ones you described, in SPSS, R, and
others as well.
In general, I think it is good to know a couple of different packages,
especially
if you plan on doing a lot
Hi Group,
Consider a data frame like this:
mylabel1 - rep(c(A,B,C),each=3)
mylabel2 - rep(c(A,B,C),3)
corrs - c(1,.8,.7,.8,1,.7,.7,.7,1)
myData - data.frame(mylabel1,mylabel2,corrs)
myData
mylabel1 mylabel2 corrs
1AA 1.0
2AB 0.8
3AC 0.7
Check out the help page of the lrm function in the rms library. To
show how lrm is used,
the examples simulate data for logistic regression. This may give you
some ideas.
On Wed, Jan 20, 2010 at 10:41 AM, omar kairan omarkaira...@gmail.com wrote:
Hi,
could someone help me with dilemma on the
Here is an example that may be helpful.
A - matrix(c(-3,5,4,-2),nrow=2,byrow=TRUE)
eigs - eigen(A)
eigs
$values
[1] -7 2
$vectors
[,1] [,2]
[1,] -0.7808688 -0.7071068
[2,] 0.6246950 -0.7071068
The eigenvectors may be scaled differently because they are not unique
(or have a
Hi List,
Here is some example data.
myDat - read.table(textConnection(group id
1 101
1 201
1 301
2 401
2 501
2 601
3 701
3 801
3 901),header=TRUE)
closeAllConnections()
corr_mat -read.table(textConnection(1 1 .5 0 0 0 0 0 0 0
2 .5 1 0 0 0 0 0 0 0
3 00 1.0 0
Your R code looks correct.
Because this is a straightforward calculation, I would be surprised if there
were any differences with SPSS. It may be worthwhile to check
if SPSS gives partial correlations or semipartial correlations. For example,
if you take the correlation between
py - resid(lm(y
Here are some options that may help you out. First,
let's put the data in a format that can be cut-and-pasted
into R.
myData - read.table(textConnection(var1 var2 var3
1 111
2 312
3 813
4 614
51015
6 221
7 422
8
Check out examples in the lattice package and ggplot2 package.
For example let's say you plot points and confidence intervals. These packages
will then allow you to plot these values by group and by combinations of groups.
Look up conditioning and faceting in these packages.
On Wed, Nov 18, 2009
Also, you probably get less data copying by using a for() or while() loop
than by using apply() in this context.
Why may there be less data copying with for and while compared to apply?
Finally, the overhead of formula parsing and model matrix construction
repeated thousands of times
I think it's helpful to show the sampling variability in a QQ plot
under repeated
sampling. An example is given
in Venables, Ripley pg 86. The variance is higher at the tails. Even when the
distributions are the same, the QQ plot does not have to resemble a straight
line because of sampling. I
Does this work for you?
data_list - list()
filepattern=modrate*
all_files - list.files(pattern=filepattern)
data_list - lapply(all_files, read.table,header=TRUE,sep=,)
__
R-help@r-project.org mailing list
https://stat.ethz.ch/mailman/listinfo/r-help
The test that a slope differs by group is a test that the
variable*group interaction equals
zero (overall test). Maybe searching post-hoc comparisons in
regression will give you some
leads.
On Tue, Sep 15, 2009 at 10:57 AM, Jun Shen jun.shen...@gmail.com wrote:
Hi, all,
I am thinking to
Do you run into problems if you use something like:
cc - rep(numeric,9)
mydata - read.table(yourdata,header=TRUE,colClasses=cc,skip=1,nrows=numRows)
__
R-help@r-project.org mailing list
https://stat.ethz.ch/mailman/listinfo/r-help
PLEASE do read the
I get a different result:
txt - c(sales to 23 August 2008 published 29 August,sales to 6
September 2008 published 11 September)
strsplit(txt, 'published ', fixed=TRUE)
[[1]]
[1] sales to 23 August 2008 29 August
[[2]]
[1] sales to 6 September 2008 11 September
sessionInfo()
R version 2.9.0
You may find the multtest package helpful. It implements methods from
Westfall and Young (Resampling based multiple testing).
On Mon, Aug 31, 2009 at 5:37 AM, Yonatan
Nissenbaumyoni@mail.huji.ac.il wrote:
Hi,
My query is regarding permutation test and reshuffling of genotype/phenotype
Check out Chapter 7 of Laura Thompson's R Companion to Agresti (you can find it
online).
It will show you how to fit proportional odds models (polr in MASS,
and lrm in the Design library) and multinomial
regression models.
__
R-help@r-project.org
Let's say that location defined a group, and observations may
be more similar in a group. You could account for this similarity
with the following model.
model1 -lme(X~CorP,random=~1|location,data=mydata,method=ML)
This fits a random intercept model grouped by location. This would
assume that
Is multinom the function you are looking for?
library(nnet)
library(MASS)
?multinom indicates that this
fits multinomial log-linear models. If you are looking for multiple
logistic regression
you may want to read up on glm or lrm from the Design package.
Could you elaborate on what you mean by
Hi Janet,
Were you able to install the package? I just installed it without
problems. I don't
think there should be any issues installing it. If it has not worked
yet, make sure your
R is updated, and if it is, maybe reinstall it.
Best,
Juliet
On Mon, Aug 17, 2009 at 8:43 PM, Janet
I'm not sure how to do this in lattice, but here is an option
with ggplot2.
library(ggplot2)
set.seed(123)
# Make sure the data has a variable that indicates
# which group is red and which one is black
DF - data.frame(x = rnorm(10), y = rnorm(10), gr = rep(1:5,
2),endpoint =
Maybe this is helpful.
Install ggplot2.
#Create a small example
x - seq(1:20)
y - (2*x) + rnorm(length(x),0,1)
id - rep(1:5,each=4)
dat - data.frame(x,y,id)
library(ggplot2)
p - ggplot(dat,aes(x=x,y=y,colour=factor(id)))
p - p + geom_point()
p
If this is not the correct structure, maybe
Hi Jack,
Maybe this helps.
# make some data
set.seed(123)
condition - factor(rep(c(a,b), each = 5))
score - rnorm(10);
lg - data.frame(condition, score)
# Carry out commands
a - subset(lg,condition==a)[score]
b - subset(lg,condition==b)[score]
t.test(a,b,paired=TRUE)
#Error in
Here are a couple of examples.
# residuals not normal
n - 100;
x = seq(n)
y = 10 + 10 *x + 20 * rchisq(n,df=2)
non_normal_lm = lm(y~x)
#non-constant variance
n - 100;
x = seq(n)
y = 100 + 3 * x + rnorm(n,0,3) * x;
het_var_lm = lm(y~x)
#For each of these try:
plot(non_normal_lm)
plot(het_var_lm)
Hi Group,
I have a question about obtaining the bias-corrected c-index using
validate from the Design library.
As an example, consider the example from help page:
library(Design)
?validate.lrm
n - 1000
age- rnorm(n, 50, 10)
blood.pressure - rnorm(n, 120, 15)
cholesterol-
Hi Group,
Create some example data.
set.seed(1)
wide_data - data.frame(
id=c(1:10),
predictor1 = sample(c(a,b),10,replace=TRUE),
predictor2 = sample(c(a,b),10,replace=TRUE),
predictor3 = sample(c(a,b),10,replace=TRUE),
measurement1=rnorm(10),
measurement2=rnorm(10))
Hi,
#make example data
dat - data.frame(matrix(rnorm(15),ncol=5))
colnames(dat) - c(ab,cd,ef,gh,ij)
If I want to get a subset of the data for the middle 3 columns, and I
know the names of the start column and the end column, I can do this:
mysub - subset(dat,select=c(cd:gh))
If I wanted to do
Here are two things to try.
First check the data. There may be a factor that does not have
variation in the sample. For example,
if you had a predictor such as 'present'/'absent', in the current
sample, all of them
may be 'present'.
Second, you can put a 'try' statement in your function.
try(
You may find the following two books useful:
Lehmann, Reminiscences of a Statistician (Springer).
David Salsburg, The lady testing tea.
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PLEASE do read the posting guide
Hi All,
I am trying to understand panel functions. Let's use this example.
library(lattice)
time-c(rep(1:10,5))
y -time+rnorm(50,5,2)
group-c(rep('A',30),rep('B',20))
subject-c(rep('a',10),rep('b',10),rep('c',10),rep('d',10),rep('e',10))
myData -data.frame(subject,group,time,y)
head(myData)
There are several things you can tell read.table to make it faster.
First, as mentioned, setting colClasses helps. I think telling read.table how
many rows and columns there are also helps.
When this was not sufficient, I've had to do the data processing
using Python, Perl, or awk.
If that had
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