similar to: Installing a package yet it will not work.

I would really appreciate it if anyone could determine what is going on with the following command. It is only half-working and is losing lots of data. For the life of me I cannot even see the pattern of what it is losing and what it is not. I am attaching the R data set which you can use with the Load Workspace menu function.

A while back Gabor Grothendieck suggested that I try http://news.gmane.org/gmane.comp.lang.r.general. This was after I asked how to easily reply to posts on the listserve. Ideally I would like the functionality that I find in Microsoft Outlook Express newsreader for usenet groups or what I find in Google Groups. I started using gmane about 3 weeks ago. I find it fantastic for searching and for

How does one create a vector whose contents is the list of variables in a dataframe pertaining to a particular pattern? This is so simple but I cannot find a straightforward answer. I want to be able to pass the contents of that list to a "for" loop. So let us assume that one has a dataframe whose name is Data. And let us assume one had the height of a group of people measured at

I am involved in a study where, as in most of life, men demonstrate themselves to be recalcitrant. So while we have many probands and most of their mothers we only have about 50% of the trios being complete. I have been running tdt and trio.types. It appears as if it is ignoring the duos. Sometimes a duo can be informative. For instance Father ..missing Mother 1/2 Proband 1/1 This duo shows that

I followed the threads that enquired about doing post-hoc tests after doing Kruskal testing. It took me to npmc. But npmc is giving an output I do not understand. I noticed a thread entitled "npmc function: 'x' must be atomic" but there never appeared to be a resolution. > npmc(npmcinput) Error in sort(unique.default(x), na.last = TRUE) : 'x' must be atomic

Bottom Line Up Front: How does one reshape genetic data from long to wide? I currently have a lot of data. About 180 individuals (some probands/patients, some parents, rare siblings) and SNP data from 6000 loci on each. The standard formats seem to be something along the lines of Famid, pid, fatid, motid, affected, sex, locus1Allele1, locus1Allele2, locus2Allele1, locus2Allele2, etc In other

I am using dgc.genetics to perform TDT analysis on SNP data from a cohort of trios. I now have a file with about 6008 variables. The first few variables related to the pedigree data such as the pedigree ID the person ID etc. Thereafter each variable is a specific locus or marker. The variables are named by a pattern such as "Genotype.nnnnn" with nnnnn corresponding to a number which

I am about one step away from heaven on earth. I think only one step! I am using dgc.genetics to run a TDT test on thousands of genetic loci. I have learnt (through the help of others on this mailing list) to send the complex output to useful data frames which in turn allow me to look at the big picture and screen the thousands of loci. Resultdt<-lapply(PGWide[,240:290], tdt) the above

Power calculations two sample test for proportions is very useful. Is there a way however, to get away from the two samples being of the same size. What would happen if one had n=15 in the one sample and n=45 in the other sample. Farrel Buchinsky, MD Pediatric Otolaryngologist Allegheny General Hospital Pittsburgh, PA **********************************************************************

Hi, I am trying to load the library(ks), but I am getting the following error: Loading required package: KernSmooth KernSmooth 2.22 installed Copyright M. P. Wand 1997 Loading required package: mvtnorm Loading required package: rgl Loading required package: misc3d Error in lazyLoadDBfetch(key, datafile, compressed, envhook) : ReadItem: unknown type 241 In addition: Warning messages: 1:

I am currently using R 2.1.1 under Windows and I do not seem to be able to load the current versions of lme4/Matrix. I have run 'update.packages.' I understand this is still experimental software but I would like access to a working version. Thanks. Chuck R Output: > library(lme4) Loading required package: Matrix Error in lazyLoadDBfetch(key, datafile, compressed, envhook) :

I am aware of the R Genetics Project that developed the R library and software called Bioconductor (http://www.bioconductor.org/ ) . How do the two relate to each other? What is the one that the other is not and vice versa? Can anybody link me to something that answers the question? -- Farrel Buchinsky, MD Pediatric Otolaryngologist Allegheny General Hospital Pittsburgh, PA

Dear R People: I wanted to use the package "its" this afternoon. I'm using R Version 2.2.0 for Windows. I was able to install the package, but ran into trouble at the "library" command. Here is the output: > library(its) Loading required package: Hmisc Hmisc library by Frank E Harrell Jr Type library(help='Hmisc'), ?Overview, or ?Hmisc.Overview') to see

Hi everyone! I get the following message anyhow I try to load the package gplots: Error in lazyLoadDBfetch(key, datafile, compressed, envhook) : ReadItem: unknown type 241 Error in library(pkg, character.only = TRUE) : package/namespace load failed for 'gplots' Could any of you tell me what goes wrong? (I am using R 2.0.1. on Windows) Thanks a lot: ----------

Hi all, I have a problem in installing and using the plm package using R 2.2.0 on windows xp. I installed it from a .zip file downloaded from the CRAN. Apparently everything is ok: > utils:::menuInstallLocal() package 'plm' successfully unpacked and MD5 sums checked updating HTML package descriptions However, when I try to load it: > library(plm) Errore in lazyLoadDBfetch(key,

Does anyone know if the sib TDT has been implemented in R 1. Spielman, R.S., and Ewens, W.J. (1998) A sibship test for linkage in the presence of association: the sib transmission/disequilibrium test. Am J Hum Genet 62, 450-458 -- Farrel Buchinsky, MD Pediatric Otolaryngologist Allegheny General Hospital Pittsburgh, PA

I would like to track in which journals articles about a particular disease are being published. Creating a pubmed search is trivial. The search provides data but obviously not as an R dataframe. I can get the search to export the data as an xml feed and the xml package seems to be able to read it. xmlTreeParse("

Hello, what does the following error mean?? It occured during or at the end of a lengthy (and memory-intensive) calculation using a routine from a shared library called via the '.C' function: Error in lazyLoadDBfetch(key, datafile, compressed, envhook) : recursive default argument reference I could not find any help with help.search("lazyLoadDBfetch") Im using R

Hi All, I want to print a square matrix of 7000 x 7000 into a text file. But I got a error after few hours of computation... -------- > write.table(MyDistMxDF, file = "temp.csv", sep=",", quote=F) *** malloc: vm_allocate(size=8421376) failed (error code=3) *** malloc[2889]: error: Can't allocate region Error: vector memory exhausted (limit reached?) *** malloc:

I tried to compile R (current R-patched to be more precise) with gcc 3.5 by Apple (which will be probably shipped with Tiger) and here's how far I got: 1) compilation itself was fine except for one exception: ../../../../../../R-patched/src/library/stats/src/starma.c: In function `forkal': ../../../../../../R-patched/src/library/stats/src/starma.c:384: error: invalid lvalue in