similar to: read in cel file by ReadAffy and read.celfile

Hi all , I have one query. i have list of some .cel files. in my program i have to mention the path of these .cel files part of my program is, rna.data<-exprs(justRMA(filenames=file.names, celfile.path=*datadir*, sampleNames=sample.names, phenoData=pheno.data, cdfname=cleancdfname(hg18_Affymetrix U133A))) in the place of "datadir" i have to mention the character string of the

Hello, After running R CMD check on my package I received the following error on package dependencies: * using log directory 'C:/z-zBackup/Nuvera Bio on Iatros01/Development/RPackages/nvNormalize/nvNormalize.Rcheck' * using R version 2.9.1 (2009-06-26) * using session charset: ISO8859-1 * checking for file 'nvNormalize/DESCRIPTION' ... OK * checking extension type ... Package *

Hello, I'm very new in working with tcl/tk in R and have a problem which will probably sound silly to most of you. Here is the code I have problems with: readcelfiles <- function() { require(tcltk) tt <- tktoplevel() tkgrid(tklabel(tt,text="Choose a directory!")) OnOK <- function() { fileDir<-tclvalue(tkchooseDirectory()) data.raw <-

Hi!I'm doing a little data importing from .cel files, > setwd("/home/mandova/celfiles") > mydata<-ReadAffy() Error in sub("^/?([^/]*/)*", "", filenames, extended = TRUE) : unused argument(s) (extended = TRUE) Then I tried > filenames<-paste("GSM",c(seq(138597,138617,1)),".cel",sep="") >

Hey, I just googled my error and many things came up. I followed the leads and read the ?read.delim page; I tried changing header = TRUE, and row.names = TRUE-- but I've still been having trouble fixing it, so I would greatly appreciate any help you can provide. Here is my code: rm(list=ls()) source("../../functions.R") uncurated <-

When I try to load cel files (hgu133a) using the ReadAffy() in R 1.8.1 command I get an error message: > x<-ReadAffy() Error: cannot allocate vector of size 102973 Kb Does anybody know what does this error mean and how to overcome it? I have tried to load the same data with R 1.7.1 and it works. There is also no error when I use R 1.8.1 to load moe430 cel files. Thanks very much for any

Hello, I want to use expresso for preprocessing the hgu133a-spikein data from affycompII. But there is an error: > library(affy) > path <- "z:/Microarray/hgu133a-spikein/rawdata" > celFile <- list.celfiles(path=path,full.names=TRUE); > affyBatch <- ReadAffy(filenames=celFile[1:6]); > eset1 <-

The control flow was: if (!y) { ppix = ... } if (y) { ... } else if (x) { use ppix for something } else { use ppix for something } Merge the if(!y) block with the two else branches. This avoids a false-positive in the clang static analyzer, it can't know that !y and x are mutually exclusive. The result looks something like this: if (y) { ... } else { ppix = ... if (x) {

Hello, I have a data frame with one column: > remove V1 1 ABAFT_g_4RWG569_BI_SNP_A10_35096 2 ABAFT_g_4RWG569_BI_SNP_B12_35130 3 ABAFT_g_4RWG569_BI_SNP_E09_35088 4 ABAFT_g_4RWG569_BI_SNP_E12_35136 5 ABAFT_g_4RWG569_BI_SNP_F11_35122 6 ABAFT_g_4RWG569_BI_SNP_F12_35138 7 ABAFT_g_4RWG569_BI_SNP_G07_35060 8 ABAFT_g_4RWG569_BI_SNP_G12_35140 I want to remove these 8

On Wed, 21 Oct 2020 16:15:22 -0500 Ana Marija <sokovic.anamarija at gmail.com> wrote: > Hello, > > I have a data frame with one column: > > > remove > > V1 > > 1 ABAFT_g_4RWG569_BI_SNP_A10_35096 > 2 ABAFT_g_4RWG569_BI_SNP_B12_35130 > 3 ABAFT_g_4RWG569_BI_SNP_E09_35088 > 4 ABAFT_g_4RWG569_BI_SNP_E12_35136 > 5

On 01/07/2013 12:51 PM, syslinux-bot for Matt Fleming wrote: > Commit-ID: 15a67011987c341814533ac4d8e23c9a72dc7605 > Gitweb: http://www.syslinux.org/commit/15a67011987c341814533ac4d8e23c9a72dc7605 > Author: Matt Fleming <matt.fleming at intel.com> > AuthorDate: Mon, 7 Jan 2013 14:42:16 +0000 > Committer: Matt Fleming <matt.fleming at intel.com> > CommitDate:

Hello, To remove the file extension it's much easier to use base R filename <- tools::file_path_sans_ext(basename(celFiles)) Hope this helps, Rui Barradas ?s 22:41 de 21/10/20, Rui Barradas escreveu: > Hello, > > This is probably because basename keeps the file extension, try instead > > > filename <- sub("(^[^\\.]*)\\..+$", "\\1",

Hello, This is probably because basename keeps the file extension, try instead filename <- sub("(^[^\\.]*)\\..+$", "\\1", basename(celFiles)) celFiles[!filename %in% as.character(remove$V1)] Hope this helps, Rui Barradas ?s 22:15 de 21/10/20, Ana Marija escreveu: > Hello, > > I have a data frame with one column: > >> remove > >

The Bioconductor core group would like to announce the 1.3 release of the Bioconductor software. There are many new packages as well as several major upgrades and fixes in older packages, and users are encouraged to check them out. Release 1.3 is intended to be operated with R version 1.8.X, which can be obtained at CRAN (http://cran.r-project.org/) -- WHAT FEATURES DOES THIS RELEASE PROVIDE?

The Bioconductor core group would like to announce the 1.3 release of the Bioconductor software. There are many new packages as well as several major upgrades and fixes in older packages, and users are encouraged to check them out. Release 1.3 is intended to be operated with R version 1.8.X, which can be obtained at CRAN (http://cran.r-project.org/) -- WHAT FEATURES DOES THIS RELEASE PROVIDE?

https://bugs.freedesktop.org/show_bug.cgi?id=63263 Priority: medium Bug ID: 63263 Assignee: nouveau at lists.freedesktop.org Summary: X server crash in nouveau_xv.c:NVPutImage (NVCopyNV12ColorPlanes) QA Contact: xorg-team at lists.x.org Severity: normal Classification: Unclassified OS: Linux (All)

Dear Help, After loading the pd.Citrus library and checking the DataFrame, I ran > the R code for: > > 1) 'oligo' > > > > {> library(pd.citrus) > Loading required package: RSQLite > Loading required package: DBI > > data(pmSequence) > > > show(pmSequence) > DataFrame with 341730 rows and 2 columns > fid sequence > <integer>

Hi all! While I am trying to read .cel files with oligo package: afbatch=read.celfiles(list.celfiles()) I get an error: Package 'pd.mirna.1.0.2xgain' was not found in the BioConductor repository How can I overcome this? Thank you in advance

I think that you misunderstood me. As far as I know, RMA does three things: background correction, quantile normalization, and summary from probes to probesets. I want the probe values after background correction and quantile normalization but before the summary. On Sat, Dec 26, 2009 at 12:07 PM, Benilton Carvalho <bcarvalh at jhsph.edu> wrote: > pm(data) > > b > > On Dec

The 'w' argument to NVCopyNV12ColorPlanes is used to index into the source image. line_len is rounded up to 8 on NV50+, so if the source image (+ left offset) is not rounded to 8, NVCopyNV12ColorPlanes could read past the end of the array and crash X. This change can cause the last few horizontal pixels of dst to not be initialized, but they should be truncated by the renderer anyways.