similar to: please help me about data format.

Hi. I was used to draw 2D plot to show distribution of my samples. It was very powerful in small samples. Recently , I handle a lot of type of samples as more 15. so, I want to use more dimention. I was used that I conduct plsda function and draw biplot, such as, p1=plsda(mw, sp) biplot(p1) How can I draw 3D graph with my data?? I don't know exactly numerical value each spot. please,

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 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

Dear developeRs, I maintain a package 'pls', which has a main fit function mvr(), and functions plsr() and pcr() which are meant to take the same arguments as mvr() and do exactly the same, but have different default values for the 'method' argument. The three functions are all exported from the name space. In the 'pre namespace' era, I took inspiration from lm() and

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

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

Hi, I have the following question about creating data frames. I want to create a data frame with 2 components: a vector and a matrix. Let me use a simple example: y <- rnorm(10) x <- matrix(rnorm(150), nrow=10) Now if I do dd <- data.frame(x=x, y=y) I get a data frame with 16 colums, but if, according to the documentation, I do dd <- data.frame(x=I(x), y=y) then str(dd)

Hopefully simple question: What is the best way to name, and treat factor columns for data that has lots of columns? This is my column list: id pID50 D.1 D.2 D.3 D.4 D.5 , etc. all the way to D.185 I was under the impression from several R examples in pls that if you name your columns like above, you should be able to simply call all the D factors with "D", instead of going in and

What function and package I use to conduct ordinal regression?? My data is composed 2colums and 180rows. The first colum indicate level of mass and second colum is intensity. So, I want to calculate how much intensity are related mass. [[alternative HTML version deleted]]

Hi list, I am looking at the data yarn in package, I don't understand what is dimension of this data set. I did the following: > library(pls) > data(yarn) > dim(yarn) [1] 28 3 > head(yarn) NIR.1 NIR.2 NIR.3 NIR.4 NIR.5 NIR.6 NIR.7 NIR.8 NIR.9 NIR.10 NIR.11 1 3.06630 3.08610 3.10790 3.09720 2.99790 2.82730 2.62330 2.40390 2.19310 2.00580 1.83790 2

Version 2.0-0 of the pls package is now available on CRAN. The pls package implements partial least squares regression (PLSR) and principal component regression (PCR). Features of the package include - Several plsr algorithms: orthogonal scores, kernel pls and simpls - Flexible cross-validation - A formula interface, with traditional methods like predict, coef, plot and summary - Functions

Version 2.0-0 of the pls package is now available on CRAN. The pls package implements partial least squares regression (PLSR) and principal component regression (PCR). Features of the package include - Several plsr algorithms: orthogonal scores, kernel pls and simpls - Flexible cross-validation - A formula interface, with traditional methods like predict, coef, plot and summary - Functions

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 <-

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 =

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, 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)

> On Jul 13, 2017, at 10:43 AM, Bert Gunter <bgunter.4567 at gmail.com> wrote: > > poly(NIR, degree = 2) will work if NIR is a matrix, not a data.frame. > The degree argument apparently *must* be explicitly named if NIR is > not a numeric vector. AFAICS, this is unclear or unstated in ?poly. I still get the same error with: library(pld) data(gasoline) gasTrain <-

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,

I have been working with the pls procedure and have problems getting the procedure to work with matrix or frame data. I suspect the problem lies in my understanding of frames, but can't find anything in the documentation that will help. Here is what I have done: I read in an 10000 x 8 table of data, and assign the first four columns to matrix A and the second four to matrix B pls <-