similar to: Porting from Linux to Windows

Hi all, I have a small program (~10k lines) that just uses elementry API (like SendMessage). It compiles under Borland C++ Builder 5.5.1 (for win exe) and under g++ with winlib. The problem is that the Builder EXE runs perfectly with WINE __BUT__ the library built with winlib does not run - spits out a segmentation faul @ line 400 (whatever that means) and some Error 139 with nothing else. All

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

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

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,

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

This is my first post here, please excuse any incorrect terms etc. I have tried to follow chapter 5 of winelib-guild.pdf, but found winemaker does not correspond to the pdf. I am using wine version 1.0-rc1. I am trying to call a Linux shared library from an unmodified windows C++ program using a ?C? interface to a DLL. I have built very simple test case that I would like help to compile. Sorry for

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: > > >

Hi All ! I have some windows-maked dll (xxx.dll for example). I want to use it on my Linux machine in my Java application. For this purpose I wrote a small wrapper around the xxx.dll by using winelib library and make it as libxxx.dll.so. Now I need load this library in my jvm (by using System.loadLibrary("xxx.dll"); ) but when I try to call any function from it I got

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

I have tried to install the pls.pcr package, but as a install newbie, I wasn't too successful. I tried the command "install.package("pls.pcr",lib="~/lib/R/",CRAN="http://mirrors.sunsite.dk/cran"). The download seemed to run smoothly, but in the end I got the response "ERROR: cannot write to or create directory '~/lib/R'" Before I try to get

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.

Hello, I have a problem with some variables in 1.8.6.0. I set on extension the following lines: exten => h, n, Set (CDR (LLP) = $ {CHANNEL (rtpqos, audio, local_lostpackets)}) ; lost packets by local end ** exten => h, n, Set (CDR (PCR) = $ {CHANNEL (rtpqos, audio, remote_lostpackets)}) ; lost packets by remote end exten => h, n, Set (CDR (ljitt) = $ {CHANNEL (rtpqos,