similar to: shell function in R

Simple illustration, > df3 <- data.frame(id=c(3,2,1,4), age=c(40,50,60,50), dose1=c(1,2,1,2), dose2=c(2,1,2,1), dose4=c(3,3,3,3))> df3 id age dose1 dose2 dose41 3 40 1 2 32 2 50 2 1 33 1 60 1 2 34 4 50 2 1 3> melt.data.frame(df3, id.var=1:2, na.rm=T) id age variable value1 3 40 dose1 12 2 50 dose1 23 1

Mango Solutions, providers of S-PLUS and R consulting, development and Training Services, are looking for consultants to join their UK-based technical team. We are looking for highly motivated individuals to work in a customer-focused environment. This is a unique opportunity to develop within a dynamic company which has been expanding rapidly and profitably since it's inception in 2002.

Hello, I have made an R script that prepares a NONMEM dataset and I would like to start the NONMEM run right after the dataset is ready. I am using windows XP, R 2.9.1 and NONMEM 6. I have prepared a run.bat file that looks like this: ---------------------------------------- call K:\nmvi\NMdirectories.bat call K:\nmvi\nmfe6 "path\control.txt" "path\output.txt"

Hi I am having some problems running a covariate analysis with my colleage using R with the NonMem program we are using for a graduate school project. R and NonMem run fine without adding in the covariates, but the program is giving us a problem when the covariate analysis is added. We think the problem is with the R code to run the covariate data analysis. We have the control stream, R code

TOP Institute Pharma (TI Pharma) has granted our proposal to set up a mechanism-based PKPD modelling platform. This platform focuses on the transfer of knowledge from academia to the pharmaceutical industry and is a collaborative effort of four excellent academic institutes and six leading global pharmaceutical industries. Unique to this platform is the availability of shared databases on

________________________________ Principal Post-Doctoral Fellow PKPD modelling platform (full time) Leiden University, Leiden, The Netherlands <javascript:doredirect();> Job description ________________________________ TOP Institute Pharma (TI Pharma) has granted our proposal to set up a mechanism-based PK-PD modelling platform. This platform focuses on the transfer of

Post-Doctoral Fellowship Modelling of Cardiovascular Safety (full time) Leiden University, Leiden, The Netherlands <javascript:doredirect();> Job description TOP Institute Pharma (TI Pharma) has granted our proposal to set up a mechanism-based PKPD modelling platform. This platform focuses on the transfer of knowledge from academia to the pharmaceutical industry and is a

Dear all, at the Division of Clinical Pharmacology at the University of Cape Town (South Africa) we are looking for highly motivated science/engineering PhD graduates to join our pharmacometrics group as a post-doctoral fellow. Pharmacometrics is an emerging discipline that applies mathematical modelling and simulation to pharmacology, aiding the interpretation of data from clinical trials,

Two Postdoctoral fellows (fulltime) Leiden University, Leiden, The Netherlands Job description ________________________________________ TOP Institute Pharma (TI Pharma) has granted our proposal to set up a mechanism-based PK-PD modelling platform. This platform focuses on the transfer of knowledge from academia to the pharmaceutical industry and is a collaborative effort of

Dear group, I am trying to prepare a NONMEM friendly dataset for population PK analysis. My patient IDs are 10 digit long and NONMEM is losing precison and rouding the last couple of digits. I need to generate unique Patient IDs fromt he current 10-digit IDs. Ihave total 250 subjects so I appreciate if anybody can suggest me a way to code this in R. Regards, Ayyappa [[alternative HTML

Hi Everyone, I have data in a long format e.g. there is one row per patient but each follow-up appointment is included in the row. So, a snippet of the data looks like this: TrialNo Drug Sex Rand Adate1 Date1 Dose1 Time1 Adate2 Date2 Dose2 Time2 B1001029 LTG M 15719 30/04/2003 15825 150 106 29/08/2003 15946 200 227 B1117003 LTG M 15734 30/04/2003 15825 200 91 03/09/2003 15951 250 217

Hi - I am fitting a probit model using glm(), and the deviance and residual degrees of freedom are different depending on whether I use a binary response vector of length 80 or a two-column matrix response (10 rows) with the number of success and failures in each column. I would think that these would be just two different ways of specifying the same model, but this does not appear to be the case.

Dear R-users, Do you know if we can use the function lme in R for log-normal distribution of parameters as used in Nonmem ? theta=theta0*exp(eta) In our model, the parameters follow the log-normal distribution so it's not reasonable to deal with normal distribution which gives us negative values in simulation Thanks for your help, Thu [[alternative HTML version deleted]]

Dear All, I want to create a dataset for a NONMEM simulation. I have a dataframe with individual PK parameters and want to create a dosing sceinario in a second dataframe. I want to merge them both so that every individiual's PK parameters are combined with the dosing scenario into one. I do not have a common variable to merge and cbind is giving error that lengths are different. I

Greetings, I used latex type code in my Rd files. The pdf version using R CMD Rd2dvi --output=PKtools.pdf --pdf --title="PKtools" PKtools man came out quite nice. However, my current HTML version does not tex the latex so there is latex code in the files and looks bad. example problem code: AIC$_c$ or \begin{itemize} \item NLME: \begin{itemize} \item population level:

Dear R users, I see a graph (shown athttps://cid-c486ebef16722625.photos.live.com/self.aspx/%e6%88%91%e5%96%9c%e6%ac%a2%e7%9a%84%e8%8a%b1/untitled.bmp) in a published paper, which is very informative and clear. But I don't know what type the graph is. It looks like a sactter plot but has the points with the same y values are seperate.. I really aprreciate it if someone can tell

I THINK YOUR A VERY SAD BUNCH OF LIFES WAISTERS On Wed, Dec 8, 2010 at 7:00 PM, <rsync-request at lists.samba.org> wrote: > Send rsync mailing list submissions to > ? ? ? ?rsync at lists.samba.org > > To subscribe or unsubscribe via the World Wide Web, visit > ? ? ? ?https://lists.samba.org/mailman/listinfo/rsync > or, via email, send a message with subject or body

https://bugzilla.samba.org/show_bug.cgi?id=7854 Summary: Abysmal sparse file performance Product: rsync Version: 3.0.7 Platform: x86 OS/Version: FreeBSD Status: NEW Severity: major Priority: P3 Component: core AssignedTo: wayned at samba.org ReportedBy: grarpamp at gmail.com

=================================================================== "Food is for eating, and good food is to be enjoyed... I think food is, actually, very beautiful in itself." Delia Smith ================================================================== Release Announcements ===================== This is the latest stable release of Samba 3.5. Major enhancements in

=================================================================== "Food is for eating, and good food is to be enjoyed... I think food is, actually, very beautiful in itself." Delia Smith ================================================================== Release Announcements ===================== This is the latest stable release of Samba 3.5. Major enhancements in