similar to: cell-based high-throughput chemical compound screens package?

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

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

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

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

Hi, when I try to import a microarray CEL batch, I get this error message: > myAB <- ReadAffy () Error in .Call("read_abatch", filenames, rm.mask, rm.outliers, rm.extra, : cannot allocate vector of length 1287151200 which, assuming the value is in bites, is below my RAM values (3 Gb recognized by Windows). The isse is, when I try to do memory.limit (size = 3000 ) the

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 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'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:

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 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, I am writing to seek some guidance regarding using Lasso regression with the R package LARS. I have introductory statistics background but I am trying to learn more. Right now I am trying to duplicate the results in a paper for shRNA prediction "An accurate and interpretable model for siRNA efficacy prediction, Jean-Philippe Vert et. al, Bioinformatics" for a Bioinformatics project

Dear Colleague, Happy New Year! As we know, codon preference among different species could be dramatically different. To enhance the expression level of a foreign protein in a particular expression system (E.coli, Yeast, Insect, or Mammalian cell), it is very important to adjust the codon frequency of the foreign protein to match that of the host expression system. One classic example is GFP

Dear Colleague, Happy New Year! As we know, codon preference among different species could be dramatically different. To enhance the expression level of a foreign protein in a particular expression system (E.coli, Yeast, Insect, or Mammalian cell), it is very important to adjust the codon frequency of the foreign protein to match that of the host expression system. One classic example is GFP

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