similar to: Unable to create directory?

Hello! I need help to use the package pls.pcr in R. I installed R in an IRIX 6.5, using the version of R 0.64.1 from sgifreeware(I didn't get to install the newest version using make). I need to use the package pls.pcr and when I give the command: # R R : Copyright 1999, The R Development Core Team Version 0.64.1 (May 8, 1999) R is free software and comes with ABSOLUTELY NO

I intend to port an R project from Linux to Windows. It involves C code that is loaded via dyn.load(). I could manage to produce a 'dll' File using cygwin which seems to be o.k. Now, using dyn.load("pcr.dll") i get: Error in dyn.load(x, as.logical(local), as.logical(now)) : unable to load shared library "c:/cygwin/home/pingu/rt-pcr/pcr.dll": LoadLibrary

Hi, Currently I have a dataset of 2400*408. And I would like to apply PCR method to study the any correlation between the tests. My current data is in data.frame and I have formed horizontal(1-407) to be the exact data, and (408) to be my results data(Yes and No) I have also binarized these Yes and No to 1 and -1s. However, when I refer to PCR manual on R, the example of yarn.pcr <-

Hello, I am trying to understand how to utilize the "mvr" function in the pls Package of R. I am utilizing the R "pls Package" document dated 18 May 2005 as guidance. My data set consists of a 12 x 12 data frame created from reading in a table of values. I have read the data in via the command: volumes <- read.table("THA_vol.txt", header = TRUE) and then

Hi everyone, I?m trying to do a spaghetti plot and I know I?m doing all wrong, It must be. What I need: 15 subjects, each with measurements over 5 different times (t1, ..., t5), and the variable that I need to represent in the spaguetti plot is given by: PCR = b0 + b1 * ti + epsilon B0, - baseline of each subject B1 - trajectory of each subject over time (so multiply by t) Epsilon - error

Hi all I am trying to build an R package, which I have successfully done many times before, but have an error I cannot trace. I hope someone can help me. Here's is some edited output (full output below if it is useful): pdunn2 at PDunnUbuntu:~/DSdata$ R CMD build GLMsData * checking for file 'GLMsData/DESCRIPTION' ... OK * preparing 'GLMsData': * checking DESCRIPTION

Hi Rosa, You pass a vector to ggplot, which expects a data.frame. I am sure you meant to do this: point7$y_point7 <- point7$beta0_7 + point7$beta1_7*point7$time + point7 $epsilon_7 ggplot(point7, aes(time, y_point7)) + geom_line() HTH Ulrik On Wed, 19 Jul 2017 at 20:37 Rosa Oliveira <rosita21 at gmail.com> wrote: > Hi everyone, > > I?m trying to do a spaghetti plot and I

I have tried to find a neat way to include graphs from R in LaTeX documents, but have not succeeded (I work with a WinEdt/MikTeX combination). The two roads I have stumbled along so far are the following: *Generate postscript files and convert them into EPS files by means of GhostScript or other not so straightforward tools. *Generate pictex files and include these. None of these solutions have

What version of R, what version of pls.pcr, and on what OS? Have you checked whether your versions of software are up to date? I get: > n <- 1350 > p <- 180 > y <- rnorm(n) > x <- matrix(sample(0:1, n*p, replace=TRUE), n, p) > fit <- mvr(x, y, method="SIMPLS", validat="none", ncomp=2) > xt <- matrix(sample(0:1, 312*p, replace=TRUE), 312,

I have a SunRay server that I am looking at to determine some sizing requirements in my department. The machine has 16G of ram and 10G of swap. Currently, I have about 4G of swap used. I am wondering if dtrace/mdb can be used to find out what lwp/processes have been swapped out? Any hints? This message posted from opensolaris.org

Hello all, I have generated a principal components regression model using the pcr() function from the PLS package (R version 2.12.0). I am getting a "non-conformable arguments" error when I try to use the predict() function on new data, but only when I try to read in the new data from a separate file. More specifically, when my data looks like this #########training data

Hi, I want to calculate PLS package in R. Now I want to calculate R, MSEP, RMSEP and R2 of PLSR and PCR using this. I also add this in library of R. How I can calculate R, MSEP, RMSEP and R2 of PLSR and PCR in R. I s any other method then please also suggest me. Simply I want to calculate these value. Thanking you. -- Nitish Kumar Mishra Junior Research Fellow BIC, IMTECH, Chandigarh, India

Hi - a newbie question, if someone can please help.... I want to change X1, X2,,.....to X.1 X.2 etc in the names below. I am using the Principal Component Regression function (pcr) and it seems to want it this way > datap3.pcr <- pcr(water ~ X, 10, data = datap3, Validation ="cv") Error in model.frame.default(formula = water ~ X, data = datap3) : invalid type (list) for

I don't know the details of pls (in the pls.pcr package, I assume), but if you use validation="CV", that says you want to use CV to select the best number of components. Then why would you specify ncomp as well? Andy > From: ryszard.czerminski at pharma.novartis.com > > When I try to use ncomp parameter in pls procedure I get > following error: > > >

How do you install a package from CRAN ? I want to install pls.pcr, so I have downloaded pls.pcr_0.1.1.tar.gz but when I try to install it using the install package(s) from local zip file(s) option it says : > install.packages(choose.files('',filters=Filters[c('zip','All'),]), .libPaths()[1], CRAN = NULL) Error in file(file, "r") : unable to open connection

Full_Name: Klaus Hermann Version: 1.5.0 OS: SUNRAY - Unix Submission from: (NULL) (213.61.59.254) if we produce a numeric vector of length 0 and want compute the sum over its elements the sum function returns 0 - this is obviously misleading. Better would be to return NA and give a corresponding warning. There should be a unified strategy to handle vectors of length 0. For example the functions

for some reason the following message seems not to have reached the list in the first try, at least I can't find it. my apologies if this is my fault: we are running R under Solaris with SunRay Terminals, which are set to 8 bit color to comply with some other software. In this configuration, X11() opens with colortype=true, i.e., it is not recognized that actually the display is only 8

Dear list, I have a question concerning the above mentioned methods in the pls package with respect to the loadings matrix produced by the call. In some work I am doing I have found that the values produced are nearly of the same magnitude but of opposite sign. When I use the example data (sensory) I find this result reproduced. I am prepared to work this through but I have a feeling that

Dear list I am using the mvr function of the package pls.pcr to compute PLS resgression using a X matrix of gene expression variables and a Y matrix of medical varaibles. I would like to obtain the R2 (sum of squares captured by the model) and Q2 (proportion of total sum of squares captured in leave-one-out cross validation) of the model. I am not sure if there are specific slots in the

Dear all, I found pls.pcr package will give different results if the data are centered and scaled using scale(). I am not sure about when I should scale my data, and whether the dependent variable should be scaled. If the dependent variable is scaled, how I give a prediction to the real data? I appreciate for any suggestions and comments. Best regards, Jinsong ===== (Mr.) Jinsong Zhao Ph.D.