similar to: [Obo-relations] Discussion summary on "original" biological parts

> From the provided documentation I understood that in memory data > structures of a PNaCl program are incompatible to the host program because > ABIs are different (e.g. PNaCl pointers are always 32-bit even when running > on x86_64 platform). > So PNaCl program can't access any data structures of the host program > directly. The only communication way is by using syscalls,

Am 19.06.2013 18:01, schrieb JF Bastien: > > From the provided documentation I understood that in memory data > structures of a PNaCl program are incompatible to the host program > because ABIs are different (e.g. PNaCl pointers are always 32-bit > even when running on x86_64 platform). > So PNaCl program can't access any data structures of the host >

Dear all, I have a collection of 5000 entries which represent the evolutionary rates of 3 animals. I would like to show the differences between the rates of all 3 animals and have tried using the function parallel (from the lattice package) and pairs() function. The parallel function would have been perfect save for the large number of data (5000). The pairs() function doesn't show

I'm trying to enter a vector into the subdiagonal of a matrix but cannot find a command in R which corresponds to the MatLab version of diag(vec, k), where vec = the vector of interest, and k = the diagonal (k=0 for the diagonal; k=-1 for the subdiagonal; k=1 for superdiagonal, etc.) Is there an equivalent command in R? I'm looking for something like this: vec = seq(1, 5, 1)

Dear List, After including cluster() option the coxreg (from eha package) produces results slightly different than that of coxph (from survival) in the following time-dependent treatment effect calculation (example is used just to make the point). Will appreciate any explaination / comment. cheers, Ehsan ############################ require(survival) require(eha) data(heart) # create weights

I am doing very regular stuff like the following: attach(wtana) fm<- lm(Body.Wt.on.SD1~Heart.Wt, data=wtana) #fm<- lm(wtana$Body.Wt.on.SD1~wtana$Heart.Wt) lrf<- loess(Body.Wt.on.SD1~Heart.Wt, wtana) #lrf<- loess(wtana$Body.Wt.on.SD1~wtana$Heart.Wt) plot(Body.Wt.on.SD1,Heart.Wt) #plot(wtana$Body.Wt.on.SD1,wtana$Heart.Wt) #lines(spline(Heart.Wt,fitted(lrf)), col=2) abline(fm, col=4)

Dear all, I want to read in 1000 files which contain varying number of columns. For example: file[1] contains 8 columns (mixture of characters and numbers) file[2] contains 16 columns etc I'm reading everything into one big data frame and when I try rbind, R returns an error of "Error in rbind(deparse.level, ...) : numbers of columns of arguments do not match" Below is my

library(glmpath) data(heart.data) # heart.data is a list, $y a vector, $x a matrix data <- data.frame(x=I(heart.data$x), y = heart.data$y) > data[1:2,] x.1 x.2 x.3 x.4 x.5 x.6 x.7 x.8 x.9 y 1 160 12 5.73 23.11 1 49 25.3 97.2 52 1 2 144 0.01 4.41 28.61 0 55 28.87 2.06 63 1 > dimnames(heart.data$x)[[2]] [1] "sbp"

I am trying to print a graph > plot(y=atestplot$b,x=atestplot$a, type="s") > win.print() This leads to a windows print dialog box- that diappears when i hit print. subquently i find a "GraphAppJob" of zero size in the print queue- this just sits until I enter dev.off() at which point a blank sheet is printed Is it me or is this a bug? Incidentally if i just

Dear All, I do apologise if this question is out of place for this list but I've tried searching mailing lists and read "Introductory Statistics with R" by Peter Dalgaard, but couldn't find any hints on solving my question below: I have a data frame (d) of values which I will rank in decreasing order of "val". Each value belongs to a group, either 'A',

Hi all, Forgive me if this question has been addressed, but I was unable to find anything in the r-help list or in cyberspace. My question is this: is there a function, or set of functions, that will enable a script to detect its own path? I have tried file.path() but that was not what I was looking for. It would be nice to be able to put all the related scripts I use in the same folder with a

Dear UseRs, Suppose I have data regarding smoking habits of a prospective cohort and wish to determine the risk ratio of colorectal cancer in the smokers compared to the non-smokers. What do I do at the end of the study with people who die of heart disease? Can I just censor them exactly the same as people who become uncontactable or who die in a plane crash? If not, why not? I'm thinking

I have data for several rings of a left heart chamber, and which I would like to display in concentric rings, with color-encoding of the values. Each ring corresponds to one slice through the heart, and the rings correspond to positions from the base to the apex of the heart as you move from the outermost ring to the innermost one. The data have a circular pattern. These types of displays are

Dear WizaRds, This is mostly a statistics question, but I'm figuring that R is the right solution (even before I start!) I have some bio data of heart rate versus time (rats taken from resting to maximal heart rate). I want to regress heart rate on time. The data have been normalized such that resting heart rate is zero at time=0, so that all curves intersect at the origin (and at the origin

Dear all, I used "which" to obtain a subset of values from my data.frame. however, I find that there is a "trace" of the values I have removed. Any suggestions would be greatly appreciate. Below is my data: d <- data.frame( val = 1:10, group = sample(LETTERS[1:5], 10, repl=TRUE) ) >d val group 1 1 B 2 2 E 3 3 B 4 4

WAY TO GO, MIKE!! Hope you get your hole fixed. If you have any extra money after your operation, please send me $250,000. I need a new house. I never thought this would happen to me but termites have eaten my entire home. All I have left is a lamp and an end table. Please help me. Thanks, reefer mike wrote: > hello i always figured this would never happen to me but my heart is

Hi everyone, I currently do some statistics about my heart rate variability. I've a CSV file which looks like this: Date Time ts_mean_RR ts_sdnn_RR ts_mean_HR ts_sdnn_HR ts_rmssd 1 20110905 07:21:50.0 1139.8298 40.3053 52.7393 2.2824 45.7958 2 20110906 07:11:37.0 1182.7333 49.1861 50.8665 2.4983 60.2329 3 20110907 07:21:31.0 1136.6028 49.4682 52.9566

>From http://bugs.r-project.org/cgi-bin/R: If you are not sure whether you have observed a bug or not, it is a good idea to ask on the mailing list R-Help by sending an e-mail to r-help at stat.math.ethz.ch rather than submitting a bug report. I'm wondering whether to submit a bug report on this: ============================================================== >

dear R wizards: is it possible to use a postscript font symbol as a plot symbol? in particular, I want to use the four postscript symbols for playing cards (club, heart, spade, diamond) as points. In LaTeX, these four are \Pisymbol{psy}{"A7} \Pisymbol{psy}{"A8} \Pisymbol{psy}{"A9} \Pisymbol{psy}{"A10} and what I would love to do is place them, at say, (x=1,y=1),

Now that MacOS is Unix-based, can Wine be run on them ? -- Andrew You can be the captain I will draw the chart Sailing into destiny Closer to the heart Closer to the Heart by Rush (A Farewell to Kings, 1977) ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~