similar to: plsr how to return my formula

Hi, With some help I learned how to use plsr(Y~x, 2, data=my) function in R (and build "my" from vector "Y" and matrix "x"). But still I have question about results interpretation. In the end I want to construct prediction function in form: Y=a1x1+a2x2 But I do not understand how to do it. Documentation do not describe this. Thanks for help. ;) [[alternative HTML

hi R help group, I have installed PLS package in R and use it for princomp & prcomp commands for calculating PCA using its example file(USArrests example). But How I can use PLS for Partial least square, R square, mvrCv one more think how i can import external file in R. When I use plsr, R2, RMSEP it show error could not find function plsr, RMSEP etc. How I can calculate PLS, R2, RMSEP, PCR,

Hello, Is there a simple way of stacking/merging two dataframes in R? I want to stack them piece-wise, not simply add one whole dataframe to the bottom of the other. I want to create as follows: x.frame: aX1 bX1 cX1 ... zX1 aX2 bX2 cX2 ... zX2 ... ... ... ... ... aX99 bX99 cX99 ... zX99 y.frame: aY1 bY1 cY1 ... zY1 aY2 bY2 cY2 ... zY2 ... ... ... ... ... aY99 bY99 cY99 ...

I am trying to generate a set of random numbers that fulfill the following constraints: X1 + X2 + X3 + X4 = 1 aX1 + bX2 + cX3 + dX4 = n where a, b, c, d, and n are known. Any function to do this? Thanks, -Ala' [[alternative HTML version deleted]]

Hi I am attempting to use plsr which is part of the pls package in r. I amconducting analysis on datasets to identify which proteins/peptides are responsible for the variance between sample groups (Biomarker Spoting) in a multivariate fashion. I have a dataset in R called "FullDataListTrans". as you can see below the structure of the data is 40 different rows representing a

Hi I am analysing a dataset of 40 samples each with 90,000 intensity measures for various peptides. I am trying to identify the Biomarkers (i.e. most significant peptides). I beleive that PLS with jack knifing, or alternativeley CMV(cross-model-validation) are multivariateThe 40 samples belong to four different groups. I have managed to conduct the plsr using the commands: BHPLS1 <-

Hi, I need your help, so I send letter to you. I have a problem about plsr in pls package. I want to show how classfied or related each ohter samples, so I tried to use plsr and biplot. But, I failed. Because, I had to change data type of my sample. Unfortunately, I didn't know how change data type. I want you to help me about that. please, help me. I show you my sample data , my scripts

Hi, this is my R-Script library(pls) file <- "C:\\TXT\\brix.txt" d <- as.matrix(read.table(file, header=T, sep=",", row.names = NULL)) plsdata <- data.frame(NIR=c(1:nrow(X))) plsdata$NIR <- I(d[,3:603]) plsdata$Brix <- d[,2] results <- plsr(Brix ~ NIR, data=plsdata) after the last string i have this error > results <- plsr(Brix ~ NIR, data=plsdata)

Hi, Newbie question about the pls package. Setup: Mac OS 10.3.9 R: Aqua GUI 1.01, v 2.0.1 I want to get R^2 and Q^2 (LOO and Leave-10-Out) values for each component for my model. I was running into a few problems so I played with the example a little and the results do not match up with the comments in the help pages. $ library(pls) $ data(NIR) $ testing.plsNOCV <- plsr(y ~ X, 6, data =

I'm new in both R and statistics. I "did my homework", I tried the archives and whatever I managed to get from the sources, but still I need assistance with the plsr package. I have a model with 2 core determinants D1 and D2, made by 3 indicators each (D1a,D1b,D1c and so on). Also I have 2 moderating variables (m1,m2), where m1 moderates D1 and m2 modarates D2. The dependent

Hello, I have a data set with 15 variables (first one is the response) and 1200 observations. Now I use pls package to do the plsr as below. trainSet = as.data.frame(scale(trainSet, center = T, scale = T)) trainSet.plsr = mvr(formula, ncomp = 14, data = trainSet, method = "kernelpls", model = TRUE, x = TRUE, y = TRUE) from the model, I wish to know the

I am having a similar problem understanding the data structure of the "yarn" dataset described in the "[R] data structure for plsr" posts. I have spectroscopic data I'd like to run through a PLSR and have read the tutorial series, but still do not understand the data format required for the code to process my data. My current data structure consists of a .csv file read into

Dear readers, can anyone give an example how to use cross-validation in the plsr package. I miss to find the number of factors proposed by cross-validation as optimum. Thank you Peter -- View this message in context: http://n4.nabble.com/cross-validation-in-plsr-package-tp1563815p1563815.html Sent from the R help mailing list archive at Nabble.com.

Hi When I call for the loadings of my plsr using the command, x <- loadings(BHPLS1) my loadings contain variable names rather than numbers. >str(x) loadings [1:94727, 1:10] -0.00113 -0.03001 -0.00059 -0.00734 -0.02969 ... - attr(*, "dimnames")=List of 2 ..$ : chr [1:94727] "PCIList1" "PCIList2" "PCIList3" "PCIList4" ... ..$ : chr

All, I am working with NIR spectral data and it was great to find that the example in ?plsr also used spectral data. Unfortunately, I am having difficulty figuring out how the "yarn" dataset is structured to allow for the plsr model to read: library(pls) data(yard) yarn.oscorespls <- mvr(density ~ NIR, 6, data = yarn, validation = "CV", method = "oscorespls")

Hi I am attempting to do a loadings plot from a plsr object. I have managed to do this using the gasoline data that comes with the pls package. However when I conduct this on my dataset i get the following error message. >plot(BHPLS1, "loadings", comps = 1:2, legendpos = "topleft", labels = "numbers", >xlab = "nm") Error in

Dear collegues, I´ ve worked with near infrared (NIR) spectroscopy to assess chemical, physical, mechanical and anatomical properties of wood. I use "The Unscrambler" software to correlate the matrix of dependent variables (Y) with the matrix of spectral data (X) and I would like to migrate to R. The matrix of spectral variables is very large (2345 columns and n lines, where n =

Error in mvr(Kd_nM ~ qsar, ncomp = 6, data = my, validation = "CV", method = "kernelpls") :   Invalid number of components, ncomp How I can fix this? [[alternative HTML version deleted]]

Hello, I thought that my Digium TDM400P would be the right hardware to support the zaptel timer, and put the following IAX.CONF entry to test, (trunk=yes) in the example below [VHAX] type=peer auth=md5 username=whoknows jitterbuffer=yes ;trunk=yes secret=terriblesecret host=4.5.6.7 qualify=1200 disallow=all allow=ulaw allow=gsm ;allow=g711u ;allow=g711a But, it didn't work. So I had to

Hello, I have a large data matrix (68x13112), each row corresponding to one observation (patients) and each column corresponding to the variables (points within an NMR spectrum). I would like to carry out some kind of clustering on these data to see how many clusters are there. I have tried the function clara() from the package cluster. If I use the matrix as is, I can perform the clara