similar to: hgu133plus2hsentrezgprobe library

Hi list! I have recently tried to take my office work home, meaning that I tried to transfer my "... .RData" workspace from my PC on my laptop. The office PC runs on Windows XP and my laptop runs on Windows Vista. I have saved the workspace at the office PC and kept it in a usb drive. When I tried to open it on my laptop I got an error: "Fatal Error: Unable to restore saved data in

Hi all, I am trying to draw a Kaplan-Meier curve and I found online that Kaplan - Meier estimates are computed with a function called km in the event package. Is there an update for that because when I choose to download packages in R,. there is no package called event, even though I have selected all the repositories. Thanks in advance, Eleni [[alternative HTML version deleted]]

Hello list, I am trying to apply the paired t.test between diseased and not diseased patients to identify genes that are more expressed in the one situation under the other. In order to retrieve the genes that are more expressed in the positive disease state I do: p.values<-c() for(i in 1:length(Significant[,1])){ p.values[i]<-try(t.test(positive[i,],negative[i,],alternative

Hi all! I am new to R and I would like to ask you the following question:How can I substitute the NA values with 0 in a data frame? I cannot find a command to check if a value is NA... Thank you very much! Eleni

Hi all, I am trying to install the package "GEOquery" in unix. I have downloaded the standard version of R and this package is not contained in the default. I know that I can select repositories under windows but I don't know how to do it in unix. Does anyone have any idea on this? Thank you in advance, Eleni [[alternative HTML version deleted]]

Hello all, I have the following problem. I want to insert blank rows in an data frame so as to make it comparable with another data frame with more rows. How can I insert these rows? If this is not solvable, then, alternatively, is it easy to delete rows from a data frame? Thanks for helping, Eleni [[alternative HTML version deleted]]

Hello R users, I am trying to run a cox model for the prediction of relapse of 80 cancer tumors, taking into account the expression of 17000 genes. The data are large and I retrieve an error: "Cannot allocate vector of 2.4 Mb". I increase the memory.limit to 4000 (which is the largest supported by my computer) but I still retrieve the error because of other big variables that I have in

Dear list, I am trying to perform a significance analysis of a microarray experiment with survival data using the {samr} package. I have a matrix containing my data which has 17816 rows corresponding to genes, and 286 columns corresponding to samples. The name of this matrix is data.matrix2. Some of the first values of this matrix are: data.matrix2[1:3,1:5] GSM36777 GSM36778 GSM36779

Hello everyone, I wanted to know if it was possible to change the color of certain leaves in a hclust object in order to make my graph more readable. I know I can color certain groups but I would like to enter a vector telling the plot function which leaves to color in which color. Thanks in advance, Eleni [[alternative HTML version deleted]]

Dear list, I am having a set of human oligo ids (H200006022 H200002025 H300004703 H200000442 H200005719 H300018350) which I want to map to Ensembl or RefSeq. I am sure R has a function to do that. I downloaded the {oligo} package and tried to use the probeNames function. Although the factor of ologo ids is an object (as the argument to probeNames should be) I retrieve the following error:

Hello list! I have a proble trying to perform a SAM analysis using the function samr from the samr package. I have put the option *center.arrays=TRUE *in order to scale all the experiments to median=0. I would like to retrieved the scaled data but it seems that samr does not return it...Does anyone have any idea on this? Thanks a lot!!! E. [[alternative HTML version deleted]]

Dear R-Help, I am using the function "topTable" from the LIMMA package. To estimate adjusted P-values there are several options (adjust="fdr" , adjust="BH") as shown below: topTable(fit, number = 10, adjust = "BH", fit$Name) I guess any of these options (fdr, BH, etc.) is using a default of FDR=0.05 which is quite conservative (i.e., very

Hello! I am crossposting this to R-help and BioC, since it is relevant to both groups. I wrote a wrapper for Entrez search utility (link for this is provided bellow), which can add some new search functionality to existing code in Bioconductor's package 'annotate'*. http://eutils.ncbi.nlm.nih.gov/entrez/query/static/esearch_help.html Entrez search utuility returns a XML document

I try to send this message To Gordon Smyth at smyth at vehi,edu.au but it bounced back, so here it is to r-help I am trying to use limma, just downloaded it from CRAN. I use R 2.0.1 on Win XP see the following: > library(RODBC) > chan1 <- odbcConnectExcel("D:/Data/mgc/Chips/Chips4.xls") > dd <- sqlFetch(chan1,"Raw") # all data 12000 > # > nzw <-

Dear list, I have been searching for a week to fit a simple linear model to my data. I have looked into the previous posts but I haven't found anything relevant to my problem. I guess it is something simple...I just cannot see it. I have the following data frame, named "data", which is a subset of a microarray experiment. The columns are the samples and the rows are the probes. I

Hi all. I've got a really dumb question for anyone. How do I write the output of a limma analysis (basically the topTable) to a text file? I want to output the topTable for the entire microarray (not really a topTable anymore I suppose..). Thanks for any advice! -Josh

Hi, I get an error indicating a missing library from the package 'Ruuid'. I suppose this means I should install RGtk. I just thought I'd document the error. Maybe a dependency entry is missing? R 2.9.0 OS X 10.5.8 Thanks, - chris > biocLite('Ruuid') Using R version 2.9.0, biocinstall version 2.4.12. Installing Bioconductor version 2.4 packages: [1] "Ruuid"

Currently, when mget() is used to get the value of a function's argument with no default value and no value in the call it returns the empty name (R_MissingArg). Is that the right thing to do or should it return 'ifnotfound' or give an error? E.g., > a <- (function(x) { y <- "y from function's environment"; mget(c("x","y","z"),

I have used merge regularly and thought I understood how it worked, but I must not. I have two dataframes with identical colnames from two different experiments, TL01 and LC01. Each dataframe has a column named "Entrez.Gene", which I have converted to "as.character" just to make sure merge is not looking at factor levels. Because I have done some filtering, the Entrez.Gene

Hi, I am relatively new to R and Bioconductor and am trying to filter the topTable that I generated of differentially expressed genes from my normlized eset file comprised of ~ 40 HG-133A Affy microarrays . I would like to see if particular probesets are represented in this list. Alternatively I would like to generate a topTable of differentially expressed genes using only specified probesets