search for: developmental

..., or only every seccond label is displayed in the output. Here is a little syntax: dd <- c(100,110,90,105,95) barplot(dd,names.arg=c('Conduct Disorders','Attention Deficit', 'Eating Disorders', 'Substance Abuse','Developmental Disorders')) My question is, if there is a chance to force a line break in each label. The result shoud look like this: Bar1 Bar2 Bar3 Bar4 Bar5 Conduct Attention Eating Substance Developmental Disorders Disorders Disorders Abuse Disor...

Is there a way to put a legend on an xyplot -- eg, something akin to the key function? Or, is there a way to get the R legend function to work on a lattice plot? To the people who have done the work on lattice and grid: Thanks for making lattice. I'm finding it very useful. Anne ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~ Anne E. York National Marine Mammal Laboratory Seattle WA 98115-0070 USA

I recently uploaded a developmental version of the Matrix package, Matrix_0.6-1.tar.gz, to CRAN where it is in the src/contrib/1.9.0/Other directory. It requires some of the packages that will appear in R-1.9.0. This version marks a major redesign of the Matrix package to use S4 classes and methods and to incorporate sparse matrix...

Hi dear all, In my laptop(ubuntu 11.10 64bit), I maintained a released R (2.14) and a developmental R, I can specify qplot(..., alpha = ) in R 2.14 , but when I try to use transparency in developmental R, I got a warning message and the plot is clearly not I want. minimal example: > qplot(data = mtcars, x = mpg, y = cyl, alpha = cyl) Warning message: In grid.Call.graphics(L_points, x$x, x$y,...

Hi dear all, In my laptop(ubuntu 11.10 64bit), I maintained a released R (2.14) and a developmental R, I can specify qplot(..., alpha = ) in R 2.14 , but when I try to use transparency in developmental R, I got a warning message and the plot is clearly not I want. minimal example: > qplot(data = mtcars, x = mpg, y = cyl, alpha = cyl) Warning message: In grid.Call.graphics(L_points, x$x, x$y,...

I built some reasonably successful tools in a graphical database for reconstructing the developmental turning points for feedback loop driven natural processes. I'm trying to move it to R and am having difficulty with the very basics, i.e. a) defining time series using time as a natural number rather than a place in a table. I was also hoping b) someone might have built some of the divers...

...suave solution in R, but I can't quite figure out the best (or even a basic) way to do it. I have a simple linear regression that is fit with lm for which I would like to estimate the x intercept with some measure of error around it (confidence interval). In biology, there is the concept of a developmental zero - a temperature under which development will not happen. This is often estimated by extrapolation of a curve of developmental rate as a function of temperature. This developmental zero is generally reported without error. I intend to change this! There has to be some way to assign error to...

Hello, Kinda confused, will CentOS new SIGs: CentOS Storage, CentOS Cloud, and CentOS Virtualization, CentOS Core,etc be a developmental path to future RHEL releases, or will they continue be an exact clone of RHEL, like Centos currently is? http://www.zdnet.com/red-hat-reveals-centos-plans-7000027812/

I am having some troubles with Xfire (installer number 43094). I am running Ubuntu 10.10. Xfire starts and I can log in, but as soon as I click something, it crashes. I'm starting with a fresh WINEPREFIX. There is nothing else installed there, and no changes in winecfg. Windows version is set to XP. First couple trys, running Wine 1.2.2 from the Ubuntu repositories:

I notice two versions on the Web site, 0.2.2 being shown as developmental. I'm building a new server that will run Icecast 1.3.11 and I'm wondering how stable Ices 0.2.2 is? Are there enough fixes in it that it's worth using it? Thanks, Hunter --- >8 ---- List archives: http://www.xiph.org/archives/ icecast project homepage: http://www.icecast.org/ To...

...look at the following and let me know if this looks reasonable; if so, it probably ought to be documented somewhere to ease initial setup. ---- The manifests, nodes, certs, and a few other configuration bits live under /etc/puppet: /etc/puppet |-- classes.txt |-- dev_classes | `-- [ a bunch of developmental or obsolete manifests ] |-- fileserver.conf |-- manifests | |-- classes | | `-- [ all of the manifests I''m using in production ] | |-- nodes | | `-- [ each of my servers, by name ] | `-- site.pp |-- puppetd.conf `-- ssl `-- [ all of puppetmaster''s keys, certs, an...

...ly saves the section I can see on the screen. Any suggestions on how to save the whole plot or manipulate the plot so I get higher resolution would be much appreciated. Thanks for your help in advance, Felicity. _______________________________________ Dr Felicity Jones Department of Developmental Biology Stanford University School of Medicine Beckman Center 279 Campus Drive Stanford CA 94305-5329 USA

Hey All, For those of you that do not know me, my name is Matthew Fredrickson and I’m the project lead for the Asterisk project. First off, I wanted to thank all of you that contribute in various ways to the project – whether it be at a developmental level, answering questions on forums and mailing lists, contributing documentation, or just generally advocating for it within your sphere of influence. It takes so many people’s efforts to make the project what it is and to sustain such a large and vibrant user and developer community. We created...

...---------------- > dfrm <- data.frame(no=c(1:100000)) > length(dfrm[,1]) [1] 100000 > fix(dfrm) > length(dfrm[,1]) [1] 34464 -------------------------------------------------------- does anybody have a quick remedy for this? i am not sure whether it is worth putting much developmental effort in solving this particular problem. however, i believe that one should be aware of it when working with large data sets. greetings from the northern edge of europe. bernd.

...brain volume ~ Diagnosis + Risk Group + (Risk Group * age : Diagnosis) - 1 thus allowing risk group age/slope terms to vary within diagnosis and omitting a nonsignificant diagnosis by risk group intercept (age was centered) interaction. i am interested in whether differences in risk groups' developmental trajectories are different for different diagnoses. the last three (of 10) fixed effect estimates are estimates for the age/slope differences between risk groups for the 3 diagnostic groups. my question is this -- how do i test if the 3 differences are statistically different from each other?...

...acted to "C:\Program Files\R\R-2.6.2\library" on my pc. I tried > nora <- read.dta("nora.dta") and got Error: could not find function "read.dta" I guess "foreign" needs to be installed. How do you do this? John Taffe Biostatistician Centre for Developmental Psychiatry and Psychology Faculty of Medicine Nursing and Health Science Monash University, Australia

...eenshot of my current desktop and stick it in a window and call it the guild wars window. I can't minimize or maximize this window, so getting back to the game doesn't happen, I must close it and restart. Has anyone else encountered this problem? I am using Linux Mint 9 with the latest wine developmental release (1.3.5). I also use compizfusion. Thanks for any help in advance.

...or how to divide the class-fate count by the original class count in the size vector to get survival probabilities seed veg = 2 / 3 seed = 0.67 veg rep = 1 / 1 veg = 1 rep rep = 1 / 2 rep = 0.5 rep veg = 1 / 2 rep = 0.5 or construct the square matrix with rows and columns in the same developmental sequence like dev<- c("seed","veg", "rep"). seed veg rep seed 0 0 0 veg 0.67 0 0.5 rep 0 1 0.5 Any help or suggestions would be appreciated. Thanks, Chris Stubben -- Los Alamos National Lab BioScience Division MS M888 Los Alamos,...

...ve a fairly good statistics background, but I am by no means a PhD level expert in statistical methods. We have used the lmer package to fit various models for the various experiments that she has done (random effects from multiple measurements for each animal or each trial, and fixed effects from developmental stage, and genotype etc). The results are fairly clear cut to me, and I suggested that she publish the results as coefficient estimates for the relevant contrasts, and their standard error estimates. However, she has read the statistical guidelines for the journal and they insist on p values. I pe...

..."NA" for these values, and the found value for those where mget finds one. Could anyone tell me how this is done efficiently? Thanks a lot in advance! Georg P.S. I am in digest mode, cc'ing the answer directly to me would be nice -- Georg Wilhelm Otto Max-Planck-Institute for Developmental Biology Spemannstrasse 35/III D-72076 Tuebingen Germany phone: +49-7071-601 401 http://www.eb.tuebingen.mpg.de