similar to: Subseting data frame based on column names

Dear all. I need to draw a scatter plot of 23 chromosome copy numbers (y axes) against chromosome and physical location within each chromosome in one plot. The data matrix looks as below: chr location copy_num 1 118345 1.320118 1 3776202 1.133879 1 4798845 0.989997 1 5350951 1.100967 . more data here . . 2 118345 2.459119 2 157739 1.915919 2 1530065 1.924372 2

Dear all. I am trying to buy a hp server to run R and to complete some other tasks with limited bugets. The r-project.org site recommended that R will run on hppa-hp-hpux. However this system is out of our buget and ML system from hp is much cheaper. Is there anybody running R on ML370 or ML 570 systems? If you can provide me with some other information related that will be appreciated.

Hello all, I have a fundamental question to ask related to clustering. As you know, when we do statistic analysis, such as t-test, or anova, we like to log transform our data to make it normally distributed. My question is shall we use signal intensity of affy chips to cluster or use log transformed data. The Dendrogram profiles are certainly different when comparing two type of the data.

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, Round(0.55,1)=0.5 Round(2.55,1)=2.6 Can this be right? Thanks, Ed [[alternative HTML version deleted]]

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

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

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

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

Because functions get called and therefore, the calling sequence matters. It?s just protecting you from yourself, but as someone pointed out, there?s a way to silence such notes. G From: Herv? Pag?s <hpages.on.github at gmail.com> Sent: Tuesday, February 6, 2024 2:40 PM To: Izmirlian, Grant (NIH/NCI) [E] <izmirlig at mail.nih.gov>; Duncan Murdoch <murdoch.duncan at gmail.com>;

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

Here's a dummy example that I think illustrates the problem: toto <- function() { if (runif(1) < 0.5) function(a) a else function(a,b) a+b } > fcn <- toto() > fcn(1,2) [1] 3 > fcn <- toto() > fcn(1,2) [1] 3 > fcn <- toto() > fcn(1,2) Error in fcn(1, 2) : unused argument (2) How can you use the returned function, if you get different arguments?

Thanks. Workarounds are interesting but... what's the point of the NOTE in the first place? H. On 2/4/24 09:07, Duncan Murdoch wrote: > On 04/02/2024 10:55 a.m., Izmirlian, Grant (NIH/NCI) [E] via R-devel > wrote: >> Well you can see that yeast is exactly weekday you have.? The way out >> is to just not name the result > > I think something happened to your

I am creating a package, and a rather long usage line for one function becomes truncated in the generated .pdf manual. Is there a way that I can prevent that truncation?

I am trying to upload into R 143 Affymetrix chips onto using R on the NIH Nimbus server. I can load 10 chips without a problem, however, when I try to load 143 I receive a error message: cannot create a vector of 523263 KB. I have expanded the memory of R as follows: R --min-vsize=10M --max-vsize=2500M --min-nsize=10M -max-nsize=50M (as specified in help in R). After running this command the

I am trying to get R to run on a Red Hat 8 system, I am running R version 1.6.2 with Tcl/Tk version 8.3.5 installed. When I try to test R from the data_sets directory I get the error message; Error in firstlib(which.lib.loc, package) : Tcl/Tk support is not available on this system Error in fileBrowser(textToShow = "Choose one CDF file" , nSelect = 1, : tcl/tk library not available

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

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") >

I have two data sets: File1.txt: Name id1 id2 id3 ... N1 0 1 0 ... N2 0 1 1 ... N3 1 1 -1 ... ... File2.txt: Group id1 id2 id3 ... G1 1.22 1.34 2.44 ... G2 2.33 2.56 2.56 ... G3 1.56 1.99 1.46 ... ... I like to do: x1<-c(0,1,0,...) y1<-c(1.22,1.34, 2.44, ...)