similar to: Profiles utility not obtaining SID

hello, when i do profiles NTUSER.DAT i see this: [$$$PROTO.HIV\Software\Policies\Microsoft\SystemCertificates\TrustedPublisher] [$$$PROTO.HIV\Software\Policies\Microsoft\SystemCertificates] [$$$PROTO.HIV\Software\Policies\Microsoft] [$$$PROTO.HIV\Software\Policies] [$$$PROTO.HIV\Software\SimonTatham\PuTTY\SshHostKeys] [$$$PROTO.HIV\Software\SimonTatham\PuTTY]

I am trying to set up a data set for a survival analysis with time-varying covariates. The data is already in a long format, but does not have a variable to signify the stopping point for the interval. The variable DaysEnrolled is the variable I would like to use to form this interval. This is what I have now: ID Age DaysEnrolled HAZ WAZ WHZ Food onARV

I still need to do some repetitive statistical analysis on some outcomes from a dataset. Take the following as an example; id sex hiv age famsize bmi resprate 1 M Pos 23 2 16 15 2 F Neg 24 5 18 14 3 F Pos 56 14 23 24 4 F Pos 67 3 33 31 5 M Neg 34 2 21 23 I want to know if there are statistically detectable differences in all of the continuous variables in

R 2.7 Windows XP I have two model that have been run using exactly the same data, both fit using glm(). One model is a linear regression (gaussian(link = "identity")) the other a quasipoisson(link = "log"). I have log likelihoods from each model. Is there any way I can determine which model is a better fit to the data? anova() does not appear to work as the models have the

hello every one, How to function more than one loop in R? I have the following problem to be solved with the a method of three loops, can you help me please? The data is attached with this message. The data is composed of two parts, cleaved (denoted by ?cleaved?) and non cleaved (denoted by ?noncleaved?). ? to access to the ith peptide, you can use X$Peptide[i] ? to access to the ith label,

Hi All, I'm hoping someone can help me with a relatively simple problem. Take the following dataset: ID Diabetes ESRD HIV Contact 1 0 0 NA 0 2 1 0 NA 0 3 NA 1 0 0 4 0 NA 0 1 5 1 1 1 0 I want to generate a

Dear all, I was testing the wonderful package APE. However upon testing a particular Newick's format tree - which I think to be a non-binary tree - it yields different result as expected. > library(ape) > tree.hiv <- read.tree(text="(rat,mouse,(human,chimp));") > is.binary.tree(tree.hiv) [1] TRUE Was that a bug in APE package? - Gundala Viswanath Jakarta - Indonesia

Hello Richard As discussed in the IRC channel, when merging a moderately large reg file (~35MB) to a hiv file (~118 MB); hivex generates a huge hiv file (~580 MB). These changes address that by creating a list of unallocated blocks and reassigning unused blocks. I used https://github.com/msuhanov/regf/blob/master/Windows%20registry%20file%20format%20specification.md as a reference for the

Hi All, I would like to use anonymous cvs, but it appears not to be working (again?). There was a discussion back in Jan-Feb about whether to continue supporting it, but it seemed that Tony Rossini got it working and the discussion left off there. Did someone decide to disable it, or is it just not working properly? Here's the details: $ cvs -d

I'm somewhat a new user and have been trying to figure out how to repeat rows a certain number of time based on a variable. Currently, the number of rows is not reflective of the number of observations. To get the number of observations (n=22 in this case), I have to multiply by the variable NoRecords for each row. So, there are actually 7 cases of cancer and 3 cases of HIV in my data, not

Over a decade ago there was a problem with model.frame when the variable names were long: https://stat.ethz.ch/pipermail/r-help/2002-August/024492.html I have similar symptoms with R 2.15.3 on Windows 7: Browse[2]> x <- model.matrix(formula(myform), p$data) Error in model.frame.default(object, data, xlev = xlev) (from mice.R#601) : object is not a matrix My attempt at a work-around

Hi All. Greetings from South Africa. I have a Samba LDAP server (v 3.022) running on Ubuntu 6.10 Its serving about 200 users, with profiles, and domain logons. I want to start server MS Access Databases on it, with the best speed performance as possible. At the moment, the back ends for these databases, are about 200+ MB, and will grow over the next few years. Basically, the share should

Hi there, I'm having a PowerBuilder aplication that connects to a Sybase data base through an ODBC. The application works fine on Windows, but I want to make it run on a Mandriva 2010.2 distribution. The fact is, I could run it on a machine with Mandriva 2010.2, but now I want to do an installation from scratch to another computer, but it does't work. The kernel version that I'm

DeaR ComRades, This is a quote from a News article in Science's 11-February issue, about competitions to model data: "For Chris Raimondi, a search-engine expert based in Baltimore, Maryland, and winner of the HIV-treatment competition, the Kaggle contest motivated him to hone his skills in a newly learned computer language called R, which he used to encode the winning data model.

Hello I am running R 1.8.1 on a Windows platform I am attempting to fit an ordinal logistic regression model, using the polr function, as described in Venables and Ripley. But when I try model4 <- polr(ypsxcat~committed + as.factor(sex) + as.factor(drugusey) + anycsw + as.factor(sex)*committed + as.factor(sex)*as.factor(drugusey)+as.factor(sex)*anycsw, data = duhray) I get a message

Dear R users, I ran into this curious problem: > d <- rnorm(100) > d.density <- density(d) > sum( d.density$x * d.density$y) [1] 2.517502 Admittedly the method of computing the mass under the density curve at line 3 is crude. But 2.5 is pretty far from 1, the value it should be. I tried a few other dataset and got similar result. Am I missing something obvious? Or is the return

I am trying to install R in Linux 8.0 and I downloaded "R-1.7.1-1.i386.rpm" and did rpm -hiv R-1.7.1-1.i386.rpm and I am getting the following message: warning: R-1.7.1-1.i386.rpm: V3 DSA signature: NOKEY, key ID 97d3544e error: Failed dependencies: libblas.so.3 is needed by R-1.7.1-1 Then I went and look for libblas (which is a linear algebra library) that I found in

Dear all, I have a undirected network (g), representing all the sexual relationships that ever existed in a model community. I also have a directed edgelist (e) which is a subset of the edgelist of g. e represents the transmission pathway of HIV. Now I would like to superimpose the picture of the sexual relationships with arrows in a different colour, to indicate where in the network HIV was

Hi everyone, I am new to R-project. I did search through the list for my problem but i can't find it. I am sorry if this question has been asked. I would like to perform a correlation analysis between a hiv data and gene expression. Basically, i have a file that contains: hiv_name, start_position, end_position, chromosome. I would like to see if these data has anything to do with the

Does anyone know of research on the effects of rounding on regression? e.g., when you ask people "How often have you _______?" you are more likely to get answers like 100, 200, etc. than 98, 203, etc. I'm interested in investigating this, but don't want to reinvent the wheel. thanks Peter Peter L. Flom, PhD Assistant Director, Statistics and Data Analysis Core Center for