search for: insuline

Hi everybody! I want to find a closer neighbourins observation. This is my code: ########################## library(klaR) library(ipred) library(mlbench) data(PimaIndiansDiabetes2) dane=na.omit(PimaIndiansDiabetes2)[,c(2,5,9)] dane[,2]=log(dane[,2]) dane[,1:2]=scale(dane[,1:2]) zbior.uczacy=sample(1:nrow(dane),nrow(dane)/2,F)

Hi I want to create a nice picture about my result of k -the nearest neighbours algorithm. Here is my easy code: ################################# library(klaR) library(ipred) library(mlbench) data(PimaIndiansDiabetes2) dane=na.omit(PimaIndiansDiabetes2)[,c(2,5,9)] dane[,2]=log(dane[,2]) dane[,1:2]=scale(dane[,1:2]) zbior.uczacy=sample(1:nrow(dane),nrow(dane)/2,F)

Hi there, >library(faraway) >pima pregnant glucose diastolic triceps insulin bmi diabetes age test 1 6 148 72 35 0 33.6 0.627 50 1 2 1 85 66 29 0 26.6 0.351 31 0 >data(pima) >pima pregnant glucose diastolic triceps insulin bmi diabetes age test 1 6 148 72 35 0 33.6

I just installed 302p1 on a client's machine (I run it on all of mine) and something is definetly wrong, can't figure out what. ssh localhost ssh_exchange_identification: Connection closed by remote host stock config files except ssh allows X11 forwarding any suggestions? Michael at Insulin-Pumpers.org

Hi! I am using the NLME package for R to modeling glucose-insuline response with Bergman's model, very similar to the example in the documentation for the NLME package. My question concerns the model for the residuals. I use a proportional model , Var(e_{ij})=(sigma_g*G(t))^2 for the glucose response and Var(e_{ij})=(sigma_i * I(t))^2 for the insulin respons...

Hello everyone, I wanted to ask if there is an R-package to fit the following Poisson regression model log(\lambda_{ijk}) = \phi_{i} + \alpha_{j} + \beta_{k} i=1,\cdots,N (subjects) j=0,1 (two levels) k=0,1 (two levels) treating the \phi_{i} as nuinsance parameters. Thank you very much -- -Tony [[alternative HTML version deleted]]

Dear all, Here is my code which am using to combine 5th column from different data sets. Here is the function to do my job genesymbol.append.file <-NULL gene.column <- NULL readGeneSymbol <- function(files,genesymbol.column=5){ for(i in fnames){ temp <- read.table(fnames,header=T,sep="\t",stringsAsFactors=F,quote="\"")

Hello, I have a problem, when I run read.fasta.pdb I get this error: pdb/seq: 1 name: dcluster.1 Error: subscript out of bounds My FASTA file is the sequence of the bovine insuline. Thanks in advance, Rg -- View this message in context: http://n4.nabble.com/problem-with-bio3d-package-tp1012116p1012116.html Sent from the R help mailing list archive at Nabble.com.

Hi, I'm having a bit of trouble with the axes in my plots. I don't like the way R does not have them cross in the origin. Is there another plot/axis function? i tried using abline as suggested by someone from this list, but in my case this gives no satisfactory result, as the abline does sometimes lie on top of the y axis and sometimes not, depending on how i scale the image... #bild16

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>From what I understand, the problem is due to people's disagreement about what the "correct" behavior should be. I'm pretty sure that the following is the correct behavior from running rsh and ssh often (both fsecure and openssh). Lets say you have a stupid script that does while 1 do sleep 1 done Called foreverSleep on your remote host: rsh remotehost

The hang-on-exit bug still hasn't been fixed in OpenSSH-3.0p1... :-( Here again is the patch to fix this bug under Linux, updated for OpenSSH-3.0p1. This has been exhaustively tested for six months now. It also add an exit delay option that can be useful. The patch does not lead to data loss under Linux. Please see the Secure NFS page (SNFS) for further details:

Newbie here... tcng version 10b I''m just learning about htb and using tcng. I am trying to make the example in Martin A. Brown''s Traffic Control with tcng and HTB HOWTO v0.5 example 2 /* * Simply commented example of a tcng traffic control file. * * Martin A. Brown <mabrown@securepipe.com> * * Example: Using class selection path. * * (If you are reading the