similar to: memory limit

Sorry, maybe it's easy but I haven't found anything useful: how can I obtain a list C that contains all the members in the list B that are not in list A? This are lists of nanes, not numbers! Thank you Gabriele Zoppoli, MD Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of Genova, Genova, Italy Guest Researcher, LMP, NCI, NIH, Bethesda MD Work: 301-451-8575

Hi how can I find, in a vector of characters, which is the most frequent one? Thanks Gabriele Zoppoli, MD Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of Genova, Genova, Italy Guest Researcher, LMP, NCI, NIH, Bethesda MD Work: 301-451-8575 Mobile: 301-204-5642 Email: zoppolig at mail.nih.gov

Hi, I want to generate a number of vectors and store them with different names, like this: x=1 while (x<100) { vector#x# = rnorm(100) x=x+1 } where each vector has, at its hand, instead of #x# a number which goes from 1 to 99. How can I do this? Thanks Gabriele Zoppoli, MD Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of Genova, Genova, Italy Guest

Hi all, if I transpose a matrix with t(data), the newly created colums do not appear to have the first row as header. How can I do to have all the newly created columns have their first row as a header? Thanks Gabriele Zoppoli, MD Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of Genova, Genova, Italy Guest Researcher, LMP, NCI, NIH, Bethesda MD Work: 301-451-8575

Dear r-help mailing list, this seems stupid, but I actually don't find the solution: if I have a vector of numbers x of length n, ranging, say, from -3 to 4, if I do barplot (x) all the values below 0 go downwards, and all the positive values go upward. How can I make them all begin from the minimum pointing upwards? Thanks! Gabriele Zoppoli, MD Ph.D. Fellow, Experimental and Clinical

Please give me just a reference where I can find something useful. In summary, I need to : - find the median of each row of a matrix - create a new matrix with each value in the first matrix divided by the median of its row - if a value "a" in the second matrix is < 1, I need to substitute it with 1/a I know that for some of you it must be overeasy, but I swear I googled for two

Hi, I'm trying to create a frequency histogram for all the values in a table, but when I try to do so, an error is returned, saying that I cannot create a histogram with an obkect of that class. Here's what I do: >library(lattice) >table<-read.table("C:/.../table",header=TRUE,sep="\t") >histogram(table) Please help me!!! Thanks Gabriele Zoppoli, MD

Hello, here is the problem: I want to demonstrate that, on average, the Pearson's correlations of a specified subset of genes from a huge list (>18,000 columns) are higher than any randomly chosen subset of that list. I would therefore like to do a number of tests between that specified subset and randomly chosen ones from the "mother" list. How could I do that? What would be

Hello! I have this problem: I want to create a Venn's diagram with three lists of genes'names. The first is all the genome, the second a subset of it comprising all mitochondrial genes, and the third including all genes that correlate with a given gene. This is what I do: > library(gplots) > A<-read.delim("F:/.../mito genes just names.txt") >

Hi, I don't know to solve this error that is returned, even though I understand it: library(plotrix) Ymd.format<-"%Y/%m/%d" gantt.info<-list(labels= c("First task","Second task (1st part)","Third task (1st part)","Second task (2nd part)","Third task (2nd part)", "Fourt task","Fifth task","Sixth

Hi I'm looking for a package to perform quality control, normalization and analysis of high throughput cell-base chemical screens. I know that the cellHTS2 package provides this for siRNA screens. Does anybody know if something like what I'm looking for exists? Thank you! Gabriele Zoppoli, MD Ph.D. Fellow, Experimental and Clinical Oncology and Hematology, University of Genova,

Hi, I've lost my mind on it... I have to scatterplot two vectors, grouped by a third variable, with two different dimensions according to whether each cell line in the plot is sensitive or resistant to a given drug, and with a different color for each of 9 tissues of origin. Here's what I've done:

Hi everybody, this is a real dummy thing. I sorted a matrix based on a given column, and what I get is right, until it comes to columns of negative and positive values; than, "order" orders everything from max to min in the negative values, and then AGAIN from max to min in the positive values!!! Why isn't everything order from max to min, and that's it? Thank you!!! Attached

Hi, I need to export a rotating plot like the one generated from the following function into a PPT slide or something that can be viewed by reviewers of a journal: library(np) library(datasets) data(faithful) f <- npudens(~eruptions+waiting,data=faithful) plot(f,view="rotate",neval=100,phi=30,main="",xtrim=-0.2) Thanks! Gabriele Zoppoli, MD Ph.D. Fellow,

Hi List, I'm trying to install aroma.affymetrix, which depend on many packages, affyio is one of them. The task is done on 32-bit Linux without problem. The same task was done on Solaris 9 with R-2.5.1 without problem. Following is the error message when installation affyio. I did try to put a file stdint.h I got from the web in the path, but got more error messages. Jun root@biostatsun1

Hello useRs, I'm trying to install bioconductor on ubuntu edgy eft and R 2.4.0. I have some error messages during installation, in particular for the package "affy" : "Error: package 'affy' required by 'makecdfenv' could not be found" I have tryed to install 'makecdfenv' with the command : getBioC("makecdfenv") But I have this message

Hi, i''m using to ziya to display some graph. If i use it running mongrel as single instance all work good (very slow but work). If i try to use it with pound as htto proxy ziya charts wait forever for data...that never arrive. If i check the mongrel log it seemes to make queries on the database and retrieve data,but nothin appera. Anyone have an idea on how i can solve this problem?

Does anyone have any input into integrating asterisk with a alcatel 4400 PBX. Acording to what i've found is that Alcatel uses R2 for E1 -- regards Vikram (http://www.vicramresearch.com)

Hallo, we have started playing with asterisk about one month ago, and we do like very much what we are experiencing. Now we would like to take some step further towards "standardizing" installed modules, functionalities, tools etc. The "wall" we are facing now is: choosing the right tool for * management. We tried AMP, very powerful but incomplete (CAPI is very important to

After a bunch of discussion in the core group, we have decided to deprecate the delay() function (which was introduced as "experimental" in R 0.50). This is the function that duplicates in R code the delayed evaluation mechanism (the promise) that's used in evaluating function arguments. The problem with delay() was that it was handled inconsistently (e.g. sometimes you would see