similar to: install on windows

How do you update R on Windows and how do you install your own package with windows interface ? regards, Ghislaine GUIGON Biostatisticienne Plate-forme 2 Puces a ADN INSTITUT PASTEUR 25-28 rue du Dr ROUX 75724 Paris cedex 15 FRANCE tel: (33) (0)1 40 61 86 51 fax: (33) (0)1 45 68 84 06

dear all, I try to update my Rversion fro 1.7.1 to 1.8.1 on linux. I have a problem when I try to install pacakges from Bioconductors with : source("http://www.bioconductor.org/getBioC.R") and getBioC(relLevel="release") somme errors append and when I make a library(affy) for example I obtain : > library(affy) Error in setIs("character",

Hi Sam, Thanks for your answer! Sorry I didn't really know how to process, but this issue block me to make some legacy C code works without having some glue with a bit static lib ;( (The change have really low risk) The changes I used locally to make dlopen/dlclose et dlsym mechanism works :) : Index: wasm/Writer.cpp =================================================================== ---

Dear R-users: I am using the package MAANOVA to analyze microarray data and have encountered problems when trying to plot data. I have tried emailing a MAANOVA discussion group, as well as the author of the package, and have not yet received a response so I am hoping that someone on this listserv can be of assistance. There are several functions in MAANOVA (riplot, resiplot) which call the

Hi, I am using "*Maanova* package" to do anova. I have created *datafile* with probeID as the first column, which is a tab limited text file and also created *designfile*. I have created *readma object* which is named as abf1. >From that readma object, i have to create data object by using *createData*function and also i hav to create model object by using *makemodel* function,

Hello, The table generated by lld (Wasm target) have a max size. So this make impossible to add some others functions in the table . As for the moment only one Table is available in WAsm this is the only way to add function in a dynamic way. Having a none static size of the table is useful for a kind dynamic loader/inker at run-time: by adding some exported functions coming from another

Hi, I run a maanova analysis and found this message error: Error in ma.svd(X, 0, 0) : 0 extent dimensions I did a google search and found this: \item ma.svd: function to compute the sigular-value decomposition of a rectangular matrix by using LAPACK routines DEGSVD AND ZGESVD. \item fdr: function to calculate the adjusted P values for FDR control. I did a search for LAPACK and

Hi I'm using a function (arrayview from the maanova package) that produces 12 plots, all in separate windows. How can I get each one to print to a jpeg file as the plots are produced? Alternatively, is it possible to get dev.print (jpeg.....) to print all open graphics devices to separate windows? Thanks in advance, Nat Street -- Nathaniel Street University of Southampton

Hello, I am basically familiar with R and am trying to import a module that someone else has written. I know that it must go into the R library but even after I place the file there R doesn't recognize it. The module is maanova, available from the Churchill lab group for analysis of microarray data, if anyone is familiar with it. Any ideas/help? Thanks, Heather --

Hi, I am trying to run an analysis with the package maanova and I am not getting success. I suppose that I am wrong on set up the formula, so the issue may not be related to R, properly. I have two varieties of plants (V1 and V2). A group of each ones were treated and another was not treated. After treatment, in three different time RNA was collected from treated and from not treated plants for

Dear R-users: I am using the package MAANOVA to analyze microarray data and have encountered problems when trying to get interactions. I am a newbie in both, R and maanova, and I do not have good knowledge in statistical methods. I have four effects: Effects Levels Var 2 Ind 2 Trat 2 Time 4 Sample 3 <-- biological replicate Spot 4 <-- technical replicate I had

Hi, I am using "*Maanova* package" to do anova. I have created *datafile* with probeID as the first column, which is a tab limited text file and also created *designfile*. I have created *readma object* which is named as abf1. >From that readma object, i have to create data object by using *createData*function and also i hav to create model object by using *makemodel* function,

Generator Microsoft Word 11 (filtered medium) Hi, I'm the mannova package maintainer. We used La.svd(X, method="dgesvd") in maanova package before. After R-2.3.0, the old La.svd() method was deprecated for option method="dgesvd". I changed maanova code correspondingly, which will call method="dgesdd" instead. But after that, we keep getting below error message

Is someone working on the infamous high frequency boost effect ? S.Gesemann published an interesting paper three months ago: http://www.xiph.org/archives/vorbis-dev/200403/att-0005/01-sq.pdf <p> -- Giuliano. --- >8 ---- List archives: http://www.xiph.org/archives/ Ogg project homepage: http://www.xiph.org/ogg/ To unsubscribe from this list, send a message to

Hi everyone, I'd like a bit of information about the stereo mode settings in psych_44.h of libvorbis. Specifically, about the adj_stereo structure: typedef struct { int pre[PACKETBLOBS]; int post[PACKETBLOBS]; float kHz[PACKETBLOBS]; float lowpasskHz[PACKETBLOBS]; } adj_stereo; What I am attempting to do is bring lossless stereo coupling down to the lower quality levels in

I wrote to the list earlier about optimizations of the tremor. Specially replacing the IMDCT with a N/4 FFT. The report is available here: http://www.sandvall.nu/thesis.pdf Short summary: Optimization of the Tremor code under 50kB for a "split" decoder version. ~44 MIPS. Huffman highly unoptimized. IMDCT ~ 8 MIPS. Quick overview of the

Hi, i just wonder if there's a cheap way of getting the number of oggVorbis pcm frames in an ogg_page, without actually decoding it? Can i use the granulepos of the page, substract the granulepos of the previous page? is this always guaranteed to work? thanks, Chris

128 kbps! In-Reply-To: <E77B14D5-B72A-11D8-91A8-000A95A4DC02@kernel.crashing.org> Message-ID: <Pine.LNX.4.44.0406081019270.6447-100000@gorlois.cs.upb.de> On Sat, 5 Jun 2004, Segher Boessenkool wrote: > There are quite a few models of how the ear works. All the good > ones are computationally expensive, and not usable at all > mathematically. Your paper uses just one simple

Hello, unfortunately I have I big problem I can't solve. I have to analyse if a gene is tissue specific. For example for the gene xyz I have following expression values: Heart Liver Brain 8.998497 10.013561 12.277407 9.743556 10.137574 11.033957 For every tissue I have two values from two different experiments. Now I want to test if Heart is significant higher

Hi, Am using maanova package for doing anova.But am getting error like this..plz, help me regarding this.. > TGR=read.madata("rmaexpr.dat",designfile="design.dat") Reading one color array. Otherwise change arrayType='twoColor' then read the data again Warning messages: 1: In read.madata("rmaexpr.dat", designfile = "design.dat") : Assume that