similar to: question on affylmGUI / oneChannelGUI

Hello, I'm trying to install oneChannelGui on my computer. For this purpose, I've tried to carefully follow the manual, and done the following: 1. I've installed the Affy power tools 2. I've installed TCL from http://www.activestate.com/Products/ActiveTcl/ (by following the link at the right side of the page, and installing activeTCL8.5.0.0) Nonetheless, when I try running

Hi, I am trying to run affylmGUI on my mac computer. I have already installed the Tlc package as well as Bwidgets through ActiveTcl conversion installing files. However, when running affylmGUI() on R, I keep getting the message in the attached file. I have copied the tcl folders from the root library to the user library, and have obtained the same issue. I would really appreciate if

Hi Bogdan, Kinda messy, but: N <- data.frame(N=c("n1","n2","n3","n4")) M <- data.frame(M=c("m1","m2","m3","m4","m5")) C <- data.frame(n=c("n1","n2","n3"), m=c("m1","m1","m3"), I=c(100,300,400))

Here's another approach: N <- data.frame(N=c("n1","n2","n3","n4")) M <- data.frame(M=c("m1","m2","m3","m4","m5")) C <- data.frame(n=c("n1","n2","n3"), m=c("m1","m1","m3"), I=c(100,300,400)) # Rebuild the factors using M and N C$m <-

Hi, please could you recommend a R package that computes a 2 sample z-test ? thanks, Bogdan [[alternative HTML version deleted]]

> On Jun 6, 2017, at 4:01 AM, Jim Lemon <drjimlemon at gmail.com> wrote: > > Hi Bogdan, > Kinda messy, but: > > N <- data.frame(N=c("n1","n2","n3","n4")) > M <- data.frame(M=c("m1","m2","m3","m4","m5")) > C <-

Dear Bert, thank you for your response. here it is the piece of R code : given 3 data frames below --- N <- data.frame(N=c("n1","n2","n3","n4")) M <- data.frame(M=c("m1","m2","m3","m4","m5")) C <- data.frame(n=c("n1","n2","n3"),

Simple matrix indexing suffices without any fancier functionality. ## First convert M and N to character vectors -- which they should have been in the first place! M <- sort(as.character(M[,1])) N <- sort(as.character(N[,1])) ## This could be a one-liner, but I'll split it up for clarity. res <-matrix(NA, length(M),length(N),dimnames = list(M,N)) res[as.matrix(C[,2:1])] <-

Thank you David. Using xtabs operation simplifies the code very much, many thanks ;) On Tue, Jun 6, 2017 at 7:44 AM, David Winsemius <dwinsemius at comcast.net> wrote: > > > On Jun 6, 2017, at 4:01 AM, Jim Lemon <drjimlemon at gmail.com> wrote: > > > > Hi Bogdan, > > Kinda messy, but: > > > > N <-

I maintain the package affylmGUI. It works when installed on many previous versions of R. I have today tested exactly the same code under R-2.15.3, R-3.0.2, R-3.1.0, R-3.1.1, R-3.1.2 and R-devel. I have also tested the versions of affylmGUI downloaded by biocLite for each version of R and the same result applies. I have no errors under 2.15.3, 3.0.2, 3.1.0 and 3.1.1. The following error

Hi, and my apologies for the following very naive question : I would like to read a column of numbers in R and plot a histogram. eg : x<-read.table("txSTART"); y<-as.numeric(x); and I do obtain the error : Error: (list) object cannot be coerced to type 'double'. Please could you let me know the way to fix it. thanks, bogdan <r-help@r-project.org> [[alternative

Dear all, please could you advise me on the following : I've written a R script that reads 3 arguments from the command line, i.e. : " args <- commandArgs(TRUE) TUMOR <- args[1] GERMLINE <- args[2] CHR <- args[3] ". when I submit the R script to a PBS HPC scheduler, I do the following (below), but ... I am getting an error message. (I am not posting the error message,

This sounds like an operating system specific question, in that "submit the R script to a PBS HPC scheduler" would be the kind of action that would run R with very different environment variables and possibly different access credentials than your usual interactive terminal. A thorough reading of the "Installation and Administration Guide" and some study of your HPC

Dear all, please could you advise on the R code I could use in order to do the following operation : a. -- I have 2 lists of "genome coordinates" : a list is composed by numbers that represent genome coordinates; let's say list N : n1 n2 n3 n4 and a list M: m1 m2 m3 m4 m5 2 -- and a data frame C, where for some pairs of coordinates (n,m) from the lists above, we have a

Dear all, please could you suggest any R functions or packages (or external programs), that a. take as input a large number (> 10 000) of short 20-30 nt sequences, and do sequence assembly, to reconstruct larger (extended) 30-50 sequences ? b. take as input a larger number of sequences (100 000 - 1 mil) and cluster these sequences in distinct classes based on the sequence similarity ?

Reproducible example, please. -- In particular, what exactly does C look ilike? (You should know this by now). -- Bert Bert Gunter "The trouble with having an open mind is that people keep coming along and sticking things into it." -- Opus (aka Berkeley Breathed in his "Bloom County" comic strip ) On Mon, Jun 5, 2017 at 6:45 PM, Bogdan Tanasa <tanasa at gmail.com>

Hi Bogdan, Messy, and very specific to your problem: df.sample.gene<-read.table( text="Chr Start End Ref Alt Func.refGene Gene.refGene 284 chr2 16080996 16080996 C T ncRNA_exonic GACAT3 448 chr2 113979920 113979920 C T ncRNA_exonic LINC01191,LOC100499194 465 chr2 131279347 131279347 C G ncRNA_exonic LOC440910 525 chr2 223777758 223777758 T A

Hi, The problem is most likely, you need to call a R CMD BATCH with your arguments and the R-script inside of a shell script that you submit to your qsub. Unfortunately we don't use qsub anymore so can't test it, but it should be as follows: R-script eg. test.R: > ##First read in the arguments listed at the command line > args=(commandArgs(TRUE)) > > ##args is now a list of

I would appreciate please a suggestion on how to do the following : i'm working with a dataframe in R that contains in a specific column multiple gene names, eg : > df.sample.gene[15:20,2:8] Chr Start End Ref Alt Func.refGene Gene.refGene284 chr2 16080996 16080996 C T ncRNA_exonic GACAT3448 chr2 113979920 113979920 C T ncRNA_exonic LINC01191,LOC100499194465

Hello, I've meanwhile got onechannelGUI running (my OS is windows). I'm trying to use it for the analysis of human exon arrays. I was able to load cel files and run them through affymetrix power tools, to obtain normalized affy data. My next step was trying to find differentially spliced exons. The menu offers to calculate either Midas or splice index scores. However, when I try to use