similar to: Q: mapped drives do not appear

When the world was young, Scott Gasch carved some runes like this: > I am having trouble with samba (version 2.0beta4) and I thought > someone might have seen this before. From client PCs (win98 > and winnt 4.0) I am able to see my samba server in net hood. I > am able to browse the shared filesystems. I am able to map > drives. However, when a network drive is mapped to a

samba@samba.org schrieb: > SAMBA Digest 1925 > > For information on unsubscribing see http://samba.org/listproc/ > Topics covered in this issue include: > > 1) UNIX to PC > by Shaun Lennox <shaun@countyfair.co.za> > 2) Connect to exported filesystem from NT via a net use cmd > by "Xia Tian"

Dear R experts I was using kinship package to fit mixed model with kinship matrix. The package looks like lme4, but I could find a way to extract p-value out of it. I need to extract is as I need to analyse large number of variables (> 10000). Please help me: require(kinship) Generating random example data id <- 1:100 dadid <- c(rep(0, 5), rep(1, 5), rep(3, 5), rep(5, 5), rep(7,

I am making the question clear. Please help. > Dear R experts > > I was using kinship package to fit mixed model with kinship matrix. > The package looks like lme4, but I could find a way to extract p-value > out of it. I need to extract is as I need to analyse large number of > variables (> 10000). > > Please help me: > > require(kinship) > > #Generating

Hi All, I'd like to ask for a few clarifications. I am doing some calculations over some biggish datasets. One has ~ 23000 rows, and 6 columns, the other has ~620000 rows and 6 columns. I am using these datasets to perform a simulation of of haplotype coalescence over a pedigree (the datestes themselves are pedigree information). I created a new dataset (same number of rows as the pedigree

I have a data frame containing the Id, Mother, Father and Sex from about 10,000 animals in our colony. I am interested in graphing simple family trees for a given subject or small number of subjects. The basic idea is: start with data frame from entire colony and list of index animals. I need to identify all immediate relatives of these index animals and plot the pedigree for them. We're

Dear R-experts Execuse me for an easy question, but I need help, sorry for that. >From days I have been working with a large dataset, where operations are needed within a component of dataset. Here is my question: I have big dataset where x1:.....x1000 or so. What I need to do is to work on 4 consequite variables to calculate a statistics and output. So far so good. There are more vector

Hello, I am building a R-package for Genetics analysis. The accepted data is in pedigree (.ped) file format. To load the data (say CAMP.ped) from "data" directory, I have a function "CAMP.R", which does the job. The package builds successfully in Linux (.tar.gz) and the data loads successfully by "data(CAMP)". However, when I build the package in WINDOWS, the data

Hello R experts, what follows is my reproducible example: mydata<-structure(list(ped.avg = c(335.9, 110.8, 645.7, 638.9, 1468.1, 126.4, 4811.1, 88.5, 868.5, 656.6, 723.6, 654, 2.8, 15, 14.2, 17.5, 15.4, 112.1, 424.7, 18.3, 19.9, 28.6, 25.6, 23.5, 15.4, 27, 62.1, 15.6, 74.6), ped.erst = c(96, 53.2, 615.2, 616.5, 512.9, 56.2, 1851.8, 57.1, 579.5, 613.2, 601.1, 613.6, 1.3, 6.3, 6.5, 6.1,

Dear R-helpers, First I apologize if my question is quite simple I have a large datasets which more 100 variables. For a research I need to change all name of variables with add one or more letters on each variables. For example, > data(Pima.tr) > Pima.tr[1:5,] npreg glu bp skin bmi ped age type 1 5 86 68 28 30.2 0.364 24 No 2 7 195 70 33 25.1 0.163 55 Yes 3 5

Dear R experts. I might be missing something obvious. I have been trying to fix this problem for some weeks. Please help. #data ped <- c(rep(1, 4), rep(2, 3), rep(3, 3)) y <- rnorm(10, 8, 2) # variable set 1 M1a <- sample (c(1, 2,3), 10, replace= T) M1b <- sample (c(1, 2,3), 10, replace= T) M1aP1 <- sample (c(1, 2,3), 10, replace= T) M1bP2 <- sample (c(1, 2,3), 10, replace= T)

Hola a todos, A partir de los siguientes datos: d <- list(`1` = structure(list(ped = c(1L, 1L, 1L, 1L, 1L, 1L, 1L), id = 1:7, father = c(2L, 0L, 0L, 2L, 2L, 2L, 2L), mother = c(3L, 0L, 0L, 3L, 3L, 3L, 3L), sex = c(2L, 1L, 2L, 2L, 2L, 1L, 2L), affected = c(1L, 2L, 1L, 1L, 2L, 2L, 2L)), row.names = c("1", "2", "3", "4", "5",

Dear all For my research, I am learning classification now. I was trying some example about classification tree pakages, such as tree and rpart, for instance, in Pima.te dataset have 8 variables (include class=type): library(rpart) library(datasets) pima.rpart <- rpart(type ~ npreg+glu+bp+skin+bmi+ped+age,data=Pima.te, method='class') plot(pima.rpart, uniform=TRUE) text(pima.rpart)

Running a PostgreSQL database and trying to understand the bottleneck in my setup. I now know there is a fdsync being issued to a database file. This one takes up to 10 seconds. The problem here is that all the other processes are entering a wait state (this is in postgres itself. The syncing process holds a latch in exclusive mode, that is needed by all others) waiting for this flush to finish.

Hi all! I am using GenABEL on R for GWAS analysis. I am having a couple of issues: First, I am having a problem reading files (.map, & .ped, size 900Mb, using windows 32-bit) onto R in the "convert.snp.ped" statement. I am thinking this problem is likely due to the large size of the files & my version of R is not able to handle them, since I can read in smaller files.

Dear R mailing list, I have a dataset with genotypes from trios and I would like to infer haplotypes for each mother, father and child. The package that I could find that can do this is tdthap. But when the mother is homozygous (e.g., 2/2) the haplotype is called as not possible to infer (0); I would prefer for it to call the genotype (2). From what I understand it is doing what I would like

Brian Ripley said that, if I sent these here, they might find their way to the R-intro team. So, here is another installment: Concerning this section: Data permanency and removing objects. This is the first place R-intro discusses objects. I was thinking a better discussion of objects and syntax is needed, perhaps here, or in the later section "Objects, their modes and attributes."

Hi Im using the kinship package to draw a pedigree. On my data set this works fine but when i add indivudals to the pedigree i keep getting an error i hope someone can help me! This is the code im using: Data<-read.table("Tree.txt", header=T, sep=",") attach(Data) ped<-pedigree(id, dadid, momid, sex, aff) par(xpd=T) plot.pedigree(ped) This is my data looks like

The issue is that delve was renamed to xapian-delve but documentation is still saying that delve is delve. Who has access to update the documentation? http://www.linuxfromscratch.org/blfs/view/svn/general/xapian.html Installed Programs: copydatabase, delve, quest, simpleexpand, simpleindex, simplesearch, xapian-check, xapian-chert-update, xapian-compact, xapian-config, xapian-inspect,

I was suggested to install two tar-red and gzip-ped packages that are not part of CRAN or BioConductors yet. I read the R manual about Administration and could only find a good description of how to install packages not canonically included in CRAN repository, on UNIX systems..... I work on Linux/SuSE and Windows ... so I am stuck with such an installation. Any suggestion in very welcome. Thank