similar to: R and XP

I'm running two Ubuntu 14.04 servers with Samba version 4.3.8-Ubuntu on each. I haven't been able to access the tools since April 15, 2016. It is setup as AD DC and all of the domain workstations CAN log in. Iv'e googled the error msgs and tried many things and have come up empty. I'm at the stage where I'm thinking of promoting dc2 and demoting dc1. I've been down a

Full_Name: Bart Version: 1.7.1 OS: XP Submission from: (NULL) (150.203.41.62) When trying to load microarray slides (gpr format) into R 1.7.1, I get the following error message Error in scan(file = file, what = what, sep = sep, quote = quote, dec = dec, : line 1057 did not have 43 elements I have been able to load the files on another computer before including an XP machine. I have

Dear R users, I'am using marray and Limma packages to analyze genepix output. 1) how can I filter bad spots from my data (data contains 3 types of bad spots). my experiment contains 12 samples and the bad spot are not associated to the same probes 2) how can I remove control probes from my data ? I'm sorry, i'm new with R and I can't find answer in packages doc. best regards,

Hello, When I launch a script under windows it does not display sequentially my cat calls or maybe the console is not refreshed at every line of my script. For instance with that code cat("\n\n================== IMPORT DATA FROM FILE ===================\n\n") fileschosen <- choose.files(caption="Select gpr files", filters = matrix(c("genepix

I have some C code (using an old Borland compiler) that calls a DLL that I'd like to get working from Windows and R (so I can read ABF files -- Axon Binary Files -- directly in R). I thought a good first approach would be able to build R in Windows, so that's what I'm trying to do. [I've done test builds of R under Linux before, and that seemed fairly simple.] I've

Hi, I''m relatively new to xen but do never the less very much like the concept & trying to run xen on a production-web-sever. "Trying" because problems start to arrise and the circumstances are rather strange: (But quit to describe) When running imagemagick from apache mysql crashes with a Signal 11. (sometimes). The other strange thing is that no swapspace at all is

Hi I'm using asterisk 1.8 Does anyone know how to use the queue reload command. The built in help doesn't really help. queue reload {parameters|membe Reload queues, members, queue rules, or parameters Regards Ish -- Ishfaq Malik Department: VOIP Support Company: Packnet Limited t: +44 (0)845 004 4994 f: +44 (0)161 660 9825 e: ish at pack-net.co.uk w: http://www.pack-net.co.uk

Dear all, I have a question about limmaGUI that is usually run in R environment. My problem is loading data into the programm. I have 6 gpr files that apparently are not compatible with limma. Everytime I'm trying to load the data (including a RNA targets file, an error appears:Error reading files. that I'm not sure,but seems to have something to do with the format of my files

Hi. Is it possible to make gpr from raw? library(aroma) #read gpr file gpr <- GenePixData$read("gpr123.gpr", path=aroma$dataPath) # gpr -> raw raw <- as.RawData(gpr) # raw -> ma ma <- getSignal(raw, bgSubtract=FALSE) ma.norm <- clone(ma) #normalization normalizeWithinSlide(ma.norm, "s") #ma -> raw raw2 <- as.RawData(ma) I want to make gpr data from

Hello, I have some files generated from microarray experiments. I used scan() to read the files, and assigned each file to a unique name with many rows and columns. Now I want to create a array (ArrayA) with unique names, and I can use ArrayA[1,2][[6]] to refer the data in each file. Is there any packages available for array of array? Thanks! [[alternative HTML version deleted]]

I encountered an bug in samba 2.0.7. With the config option "logon home = \\%N\%U\profile" in smb.conf and roaming profiles, smbd panics when the share "%U" is not listed in smb.conf. I had some users for which i forgot to enter the accompanying share in smb.conf. When such a user logged in or logged off, smbd paniced with signal 11. While on logging off the profiles where

Hi All I have been struggling with this model for some time now and I just can't get it to work correctly. The messages I get when running the code is: DLSODA- Warning..Internal T (=R1) and H (=R2) are such that in the machine, T + H = T on the next step (H = step size). Solver will continue anyway. In above message, R = [1] 0 0 DINTDY- T (=R1) illegal In above message, R = [1]

This is exactly what I want. I have a continuous stream to a live mountpoint that needs to be metadata updates. Is this http request you mention any documentation to study? El 02/09/10 08:43, Johann Soukup escribi?: > Hi Octavio, > > I guess you are talking about live mount points. > > We use a http request through the admin/metadata application of the > Icecast admin

Dear list members, I am analysing my microarray data using limma package. Now I encounter several problems. Looking forward to your suggestions! Question 1: During the process of background correction using method="normexp", four warning messages appeared as "NaNs produced in: log(x)" (as you can see in the program posted below). What does that mean? How will it effect the

Hi, I'm working with custom slides(Cy5) and working in the normalization of the arrays. I have three arrays (technical replicates). I have sucesfully normalized the data using vsn, however i would like to normalize using spike in controls. My controls are annotated as CTL-1 to x and i would like to do etiher a normalization by block per array or the mean of all the controls per array. The gal

Hi there. Anybody knows how can I send metadata updates to a running mountpoint in Icecast? Thanks -- __________________________________________________________ | , , | | / \ | | ((__-^^-,-^^-__)) Octavio Rossell Tabet | | `-_---' `---_-' octavio at

I have just spent a day trying to determine why I seemed to be unable to read a file of microarray expression results into R properly. The file was produced by the Dchip software developed by Li and Wong at Harvard's Department of Biostatistics. It contains rows of tab-delimited fields in the order Probe set identifier Probe set description Array 1 expression Array 1 call Array 2 expression

Hi Everyone, I have been trying to read some Arrayvision files( 2 channel cDNA) and am having some problem. My code is : setwd('C:/work/data/limma/ndd1'); files <- c('ndd1_1.txt','ndd1_2.txt','ndd1_3.txt'); RG=read.maimages(files,"arrayvision",sep="\t"); #Normalisation MA=normalizeWithinArrays(RG); #plotPrintTipLoess(MA); #Fit Linear

Dear R-Tech Support Team, I was just browsing on your web page and I am curious about R's system requirements. How many MB RAM and what processor speed would you recommend for Win XP if I want to load QuantArray Excel output files of appr. 16 MB each? Thank you very much in advance, Derk Bemeleit ----------------------------------------------- A--------T T-------A Dipl.-Biol.

Hello, I had a raid1 btrfs (540GB) on vanilla 3.6.3, a disk failed, and removed it at power off, plugged in a new one, partitioned it (to 110GB, by error), and added it to btrfs. I tried to remove the missing device, and it said "Input/output error" after a while. Next attempts simply gave "Invalid argument". I repartitioned, rebooted the system, and made the partition grow: