similar to: Assigning colnames in loop

Dear R-users, I would like to maximize the function g above which depends on 4 parameters (2 vectors, 1 real number, and 1 matrix) using optim() and BFGS method. Here is my code: # fonction to maximize g=function(x) { x1 = x[1:ncol(X)] x2 = x[(ncol(X)+1)] x3 = matrix(x[(ncol(X)+2):(ncol(X)+1+ncol(X)*ncol(Y))],nrow=ncol(X),ncol=ncol(Y)) x4 = x[(ncol(X)+1+ncol(X)*ncol(Y)+1):length(x)]

Hi, I am new to clustering and was wondering why pvclust using "maximum" as distance measure nearly always results in p-values above 95%. I wrote an example programme which demonstrates this effect. I uploaded a PDF showing the results Here is the code which produces the PDF file: ------------------------------------------------------------------------------------- s <-

Dear R-users I have a problem choosing initial points for the function arms() in the package HI I intend to implement a Gibbs sampler and one of my conditional distributions is nonstandard and not logconcave. Therefore I'd like to use arms. But there seem to be a strong influence of the initial point y.start. To show the effect I constructed a demonstration example. It is reproducible

Deal all, as MCMClogit does not allow for the specification of several chains, I have run my model 3 times with different random number seeds and differently dispersed multivariate normal priors. For example: res1 = MCMClogit(y~x,b0=0,B0=0.001,data=mydat, burnin=500, mcmc=5500, seed=1234, thin=5) res2 = MCMClogit(y~x,b0=1,B0=0.01,data=mydat, burnin=500, mcmc=5500, seed=5678, thin=5) res3 =

Hi, I am trying to run the command "forward.sel.par," however I receive the error message: "Error: could not find function 'simpleRDA2'." I have the vegan library loaded. The documentation on "varpart" has not helped me to understand why I cannot call this function. Maybe I am missing something obvious because I am still an 'R' novice. Below is a

Hi, I am writing an Sweave document and am using 'xtable' to make frequency tables of diagnoses of people undergoing cholecystectomy. Some of these diagnoses contain Danish characters ("?", "?", and "?"), and these characters are all garbled in the Latex document after I run Sweave. The odd thing is, everything looks absolutely right in the R console, and if

Some additional fields from the EDD-4 spec. draft for the Device Parameter Table have been added into the structure in setup.c and memdisk.inc. These were added in the hopes of resolving a FreeDOS MEMDISK bug on IBM ThinkPads. --- memdisk/memdisk.inc | 11 +++++++++++ memdisk/setup.c | 10 ++++++++++ 2 files changed, 21 insertions(+), 0 deletions(-) diff --git a/memdisk/memdisk.inc

In the manual page for prcomp(), it says that sdev is "the standard deviations of the principal components (i.e., the square roots of the eigenvalues of the covariance/correlation matrix, though the calculation is actually done with the singular values of the data matrix)." ?However, this is not what I'm finding. ?The values appear to be the standard deviations of a reprojection of

Hello R community, I am trying to combine two CSV files that look like this: File A Row_ID_CR, Data1, Data2, Data3 1, aa, bb, cc 2, dd, ee, ff File B Row_ID_N, Src_Row_ID, DataN1 1a, 1, This is comment 1 2a, 1, This is comment 2 3a,

HI, Using c11<- 0.01 c12<- 0.01 c1<- 0.10 c2<- 0.10 One possible problem is that: dim(res5) #[1] 513? 20 res6<-aggregate(.~m1+n1+m+n,data=res5[,c(1:6,9:12,21:24)] ,max) #Error in `[.data.frame`(res5, , c(1:6, 9:12, 21:24)) : ?# undefined columns selected A.K. ________________________________ From: Joanna Zhang <zjoanna2013 at gmail.com> To: arun <smartpink111 at

Dear R-help, I'd like ask for your opinion on choosing the "right" strategy for a particular dataset. We conducted 24-hour electric field measurements on 90 subjects. They are grouped by job (2 categories) and location (3 categories). There are four exposure metrics assigned to each subject. An excerpt from the data: n job location M OA UE all 0 job1 dist_200 0.297 0.072 0.171

Hi, the following R lines work fine in R 2.4.0, but not in R 2.4.1 or any devel versions of R 2.5.0 (see below for details). library(drc) # to load the dataset 'PestSci' library(nlme) ## Setting starting values sv <- c(0.43355869, 2.49963220, 0.05861799, 1.73290589, 0.38153146, 0.24316978) ## No error m1 <- nlme(SLOPE ~ c + (d-c)/(1+exp(b*(log(DOSE)-log(e)))), fixed =

Hi, (Please use ?dput() to share the example dataset. Avoid using images to show dataset. Also, please read the posting guide esp. regarding home work, assignments etc.) res <- sapply(Gene[,-1],function(x) tapply(x,list(Gene$Genotype),mean)) #or res2 <-? aggregate(.~Genotype, data=Gene,mean) #or library(plyr) ?res3 <- ddply(Gene,.(Genotype),numcolwise(mean)) identical(res2,res3)

Dear all! I have a data frame composed by 13 columns (year, and 12 months). I want to transform this data base in another like this year month values 1901 1 1901 2 1901 3 ..... 1901 12 1902 1 1902 2 .... 1902 12 Is there a possibility to succeed that in R? Thank you! best regards! CR -- --- Catalin-Constantin ROIBU Lecturer PhD, Forestry engineer Forestry Faculty of Suceava Str.

Thank you very much for your reply. Your code work well with this example. I modified a little to fit my real data, I got an error massage. Error in split.default(x = seq_len(nrow(x)), f = f, drop = drop, ...) : Group length is 0 but data length > 0 On Thu, Jan 31, 2013 at 12:21 PM, arun kirshna [via R] < ml-node+s789695n4657196h87@n4.nabble.com> wrote: > Hi, > Try this: >

Hi, Suppose, if I create 15 files in my working directory. set.seed(48) lapply(1:15,function(i) {m1 <- matrix(sample(1:20,1686*2,replace=TRUE),nrow=1686,ncol=2); write.table(m1,paste0("file_",i,".txt"),row.names=FALSE,quote=FALSE)}) ?D <-dir() D1 <- D[order(as.numeric(gsub("\\D+","",D)))] D1 ?res <- t(sapply(D1,function(x) {x1<-

Dear list members, is it intentional that: curve(cos, xlim = c(-5, 5)) plot(cos, xlim = c(-5, 5)) produce different plots? Shouldn't the 'xlim' argument in both cases set the 'from' and 'to' argument if they aren't supplied (at least that's what I understood reading the help page for 'curve' and 'plot.function')? Christian >

Dear friends - I am trying to understand fda and working with the 2009 book from Springer. I run the scripts directly from a new installed fda library and include sessionInfo() below. This is from the script fdarm-ch09.R - I seem to have got not fda_2.2.8 but 2.2.7 - is that the problem? Where do I get .8 as I just reinstalled? Best wishes Troels Ring, Nephrology Aalborg, Denmark >

Hi, I'm trying to use pgamma() within my C application but I'm getting strange results. I have a Debian system with r-mathlib 1.4.1-1 and gcc 2:2.95.4-9. Here are 3 example pgamma() calls executed by R: $ R -q --vanilla < gamma.R > pgamma(98, 100, 1) [1] 0.4333105 > pgamma(21, 100, 5) [1] 0.7002453 > pgamma(2, 100, 69) [1] 0.9997046 > and here is what the small C

Dear R-listers, I am using R for Windows Vista 64-bit. I have no experience working with maps, but now I have to plot a map of Denmark in which each Danish county is color-coded according to its incidence rate of a particular disease. My problem is that I don't know where to start. I have read the help files to packages like 'mapplot', and their examples indicate that I am on the