similar to: manipulating strings

Hi, Am I hitting some limit in match? Consider the following example: > tst<-seq(100,125,by=.2)%in%seq(0,800,by=.1) > sum(tst) [1] 76 > seq(100,125,by=.2) [1] 100.0 100.2 100.4 100.6 100.8 101.0 101.2 101.4 101.6 101.8 102.0 102.2 [13] 102.4 102.6 102.8 103.0 103.2 103.4 103.6 103.8 104.0 104.2 104.4 104.6 [25] 104.8 105.0 105.2 105.4 105.6 105.8 106.0 106.2 106.4 106.6 106.8

Hi, Am I hitting some limit in match? Consider the following example: > tst<-seq(100,125,by=.2)%in%seq(0,800,by=.1) > sum(tst) [1] 76 > seq(100,125,by=.2) [1] 100.0 100.2 100.4 100.6 100.8 101.0 101.2 101.4 101.6 101.8 102.0 102.2 [13] 102.4 102.6 102.8 103.0 103.2 103.4 103.6 103.8 104.0 104.2 104.4 104.6 [25] 104.8 105.0 105.2 105.4 105.6 105.8 106.0 106.2 106.4 106.6 106.8

Hi It clear that to do a classification with svm under 10-fold cross validation one uses svm(Xm, newlabs, type = "C-classification", kernel = "linear",cross = 10) What corresponds to the nnet? nnet(.....,cross=10)? Regards

I use a 32 bit machine. For those using 64 bit machines, what is the .Machine$double.xmin for for machines? regards. Stephen. ----- Original Message ----- From: Achim Zeileis <Achim.Zeileis at wu-wien.ac.at> Date: Tuesday, July 12, 2005 10:51 am Subject: Re: [R] exact values for p-values - more information. > On Tue, 12 Jul 2005, S.O. Nyangoma wrote: > > > > If they

I have a large data matrix (4460X3500) and I want to sum row subsets in groups of 10 (bin). Is there an efficient way to do this in R without using loops. Looping takes forever to perform this task! For example suppose we have the matrix > matrix(1:12,6,2) [,1] [,2] [1,] 1 7 [2,] 2 8 [3,] 3 9 [4,] 4 10 [5,] 5 11 [6,] 6 12 my problem is to sdum for

Dear colleague, Just an e-mail to know if they are people working in the field of chemoinformatic that are using R in their work. If yes I was wondering if we couldn't exchange tips and tricks about the use of R in this area ? Best regards Fred Ooms [[alternative HTML version deleted]]

Hi I want to install eda library. Where can I download it? I use R version 2.1.0 on Linux. Thanks. Stephen. ----- Original Message ----- From: Luis Ridao Cruz <Luisr at frs.fo> Date: Tuesday, September 13, 2005 1:32 pm Subject: Re: [R] How to erase objects > ?rm > > > >>> <v.schlecht at arcor.de> 13/09/2005 12:08:55 >>> > > Hi, I admit that

Hi there, If I do an lm, I get p-vlues as p-value: < 2.2e-16 This is obtained from F =39540 with df1 = 1, df2 = 7025. Suppose am interested in exact value such as p-value = 1.6e-16 (note = and not <) How do I go about it? stephen

Dear list, I cannot figure out why, after sub-setting my data, that particular item which I don't want to plot is still in the newly created subset (please see example below). R somehow remembers what was in the original data set. A work around is exporting and importing the new subset. Then it's all fine; but I don't like this idea and was wondering what am I missing here? Thanks!

I have a dataset that is basically structureless. Its dimension varies from row to row and sep(s) are a mixture of tab and semi colon (;) and example is HEADER1 HEADER2 HEADER3 HEADER3 A1 B1 C1 X11;X12;X13 A2 B2 C2 X21;X22;X23;X24;X25 A3 B3 C3 A4 B4 C4 X41;X42;X43 A5 B5 C5 X51 etc., say. Note that a blank

Hi R-users, I have missing data for the month. My question is how do I insert the missing month and fill up the cell with 'na' for the rain amount?  Then I would like to count the percentage of missing data. No     Year     month rain 1398 1985    10 104.2 1399 1985    11 138.0 1400 1985    12 120.4 1401 1986     1  12.6 1402 1986     2  19.4 1403 1986     3   1.0 1404 1986     4  58.8

hi Michael, am sorry for the incomplete reply . csv file data havinmg like this , >getSymbols("IBM") >weekly_data = to.weekly(week_name) >dataframe=data.frame(weekly_data) >outputfile_name="F:\\R-programs\\Outputfile.csv" >write.table(dataframe, file =outputfile_name,sep = ",",col.names =TRUE,row.names = T) > datafrom_table <-

I'm not sure when this happened. In yesterday dovecot-1.1 hg if pop3 is compiled with DEBUG defined, it needs GDB=1 otherwise it ends with: Panic: Leaked file fd 4: dev 104.2 inode 3342766 Not sure if this can be caused by the fact that I call pop3 with a bash script. protocol pop3 { mail_executable = /usr/libexec/dovecot/pop3.sh inside I've something like if [ x`id -un` =

Hello! In the guidelines I've read: "Comment your code. Entire commented lines should begin with # and one space. Short comments can be placed after code preceded by two spaces, #, and then one space. " Just wondering if there is no way to comment something out "in the middle" of a line? Example: Original code: mystrings<-c("a","b","c")

Hi, I have a question about estimating IRT models by using nlme, not just rasch model, but also other models. Behavior Research Methods <http://www.springerlink.com/content/1554-351x/> Volume 37, Number 2 <http://www.springerlink.com/content/1554-351x/37/2/>, 202-218, DOI: 10.3758/BF03192688 Using SAS PROC NLMIXED to fit item response theory models (2005). Ching-Fan

> I finally got a Best Power Patriot Pro II fixed up with a new battery and cable, and tried it with nutdrv_qx (since it uses a variant of the Q1 protocol). It auto-detected the use of Q1. > > It looks like things mostly work: Nice, merging bestups.c into nutdrv_qx has been on my todo list for a while, let's see how far we can get. > 1) The bestups driver uses an "ID"

Hi there, If I do an lm, I get p-vlues as p-value: < 2.2e-16 Suppose am interested in exact value such as p-value = 1.6e-16 (note = and not <) How do I go about it? stephen

I apologize that I've asked a similar question before, but being new to R I don't think I did a very good job of formating the question. I've included a text file since the date set is somewhat large. What I have is a huge string of numbers in a text file. The numbers are all separated by comma's and the groups are separated by a semicolon. What I would like to do is read each

I have a set of data that comprises genome numbers in single eggs from three different parasite clones - 3D7, HB3, and MIX. I can draw a boxplot of the genome numbers for each clonefed but how do I carry out a t test or ANOVA to compare if the means are signifcantly different? (Data is listed below) Many thanks, Georgina Humphreys clonefed genomes HB3 21.3 HB3 23.5 HB3 25.9 3D7 27.2 HB3 28.1

I am trying to fit a nonlinear regression to infiltration data in order to determine saturated hydraulic conductivity and matric pressure. The original equation can be found in Bagarello et al. 2004 SSSAJ (green-ampt equation for falling head including gravity). I am also VERY new to R and to nonlinear regressions. I have searched the posts, but am still unable to determine why my data come up