An Introduction to ChemoSpec2D

# R options & configuration:
set.seed(9)
rm(list = ls())
suppressMessages(library("knitr"))
desc <- packageDescription("ChemoSpec2D")

# Stuff specifically for knitr:
#opts_chunk$set(eval = FALSE)

This vignette is based upon ChemoSpec2D version r desc$Version.

Background

ChemoSpec2D is designed to analyze 2D spectroscopic data such as COSY and HSQC NMR spectra using appropriate chemometric techniques. It deploys methods aimed primarily at classification of samples and the identification of spectral features which are important in distinguishing samples from each other. ChemoSpec2D stores and manipulates each spectrum as a matrix of data, and hence a data set is a collection of 2D spectra. Thus the entire data set is naturally visualized as a 3D array with dimensions:

[ \mathrm{F2} \times \mathrm{F1} \times \mathrm{no. \ samples} ]

or

[ \mathrm{2D \ Spectrum} \times \mathrm{no. \ samples} ]

where F2 and F1 are NMR-speak for the x- and y-axes/dimensions. We will refer to this array as $\underline{\mathbf{X}}$. See Figure \@ref(fig:array).

knitr::include_graphics("3Darray.png")

ChemoSpec2D treats each spectrum/matrix as the unit of observation, and thus the physical sample that went into the spectrometer corresponds to the sample from a statistical perspective. Keeping this natural unit intact during analysis is referred to as a strong multi-way analysis. In a weak analysis, the 3D data set is unfolded into a series of contiguous 2D matrices and analyzed using methods suitable for any 2D data set (such methods are fundamentally bilinear) (@Huang2003). In the weak approach, each slice of a 2D spectrum becomes just another 1D spectrum, and the relationship between the slices in a single 2D spectrum is lost. Oddly enough, the trilinear/strong analysis has fewer parameters to estimate so it is simpler, but computationally more demanding. The interpretation is also more straight-forward. These techniques are akin to PCA, and seek to reduce the data to a limited number components represented by scores and loadings. As with PCA, noise in the data set is reduced, and correlating variables are collapsed.

The literature on the topics of chemometric analysis of 3D data sets uses a wide variety of terminology to describe analysis options, and the same mathematical analysis can be found under different guises in different fields. Here are some of the terms relevant to ChemoSpec2D:

Keirs provides discussion and suggestions on terminology best practices (@Kiers2000).

PARAFAC

Theory (Light)

PARAFAC is "parallel factor analysis." This is a statistical technique that is somewhat analogous to PCA. Recall that PCA decomposes a 2D data set into scores and loadings, and is bilinear:

[ \mathbf{X}^{(n \ \times \ p)} = \mathbf{C}^{(n \ \times \ R)} \times \mathbf{S}^{(R \ \times \ p)} + \mathbf{E} ]

Where $\mathbf{X}$ is the raw data, composed of $n$ samples $\times$ $p$ frequencies, $\mathbf{C}$ are the scores, and $\mathbf{S}$ are the loadings. $R$ is the number of components selected. $R$ is very much smaller than $p$, as noise and correlating variables have been reduced. Matrix $\mathbf{C}$ can be thought of as "concentrations" or weights. Matrix $\mathbf{S}$ is composed of "spectra" which serve as loadings. $\mathbf{E}$ consists of residuals/error. The goal of the PCA algorithm is to solve this equation and return $\mathbf{C}$ and $\mathbf{S}$.

In comparison, PARAFAC decomposes a 3D data set into three matrices, and is trilinear. Because the data is 3D, standard matrix algebra cannot be applied. However, the math can be expressed as a summation:

[ x_{ijk} = \sum_{r = 1}^{R} a_{ir}b_{jr}c_{kr} + \epsilon_{ijk} ]

Where $x_{ijk}$ is an element of the 3D data array $\underline{\mathbf{X}}$. $a_{ir}$ is an element of the matrix $\mathbf{A}$, and so forth for $b$/$\mathbf{B}$ and $c$/$\mathbf{C}$. $\epsilon$ is the error term.

If $\underline{\mathbf{X}}$ is flattened by taking the $K$-dimension slices and concatenating them left-to-right to give a matrix $\mathbf{X}$, then 2D matrix operations can provide a solution:

[ \mathbf{X} = \mathbf{A}(\mathbf{C} \odot \mathbf{B})^T + \mathbf{E} ]

Here, $\odot$ represents the Khatri-Rao product, a matrix multiplication variant needed in this situation. $\mathbf{A}$, $\mathbf{B}$ and $\mathbf{C}$ are the component matrices as above (@Bro2003b, @Smilde2004 Appendix 4.A presents a number of alternative notations for PARAFAC). If you want to dig into the math, Kolda and Bader is the go-to source (@Kolda2009).

Interpretation

Regardless of the mathematical representation or algorithmic solution, the results provide $\mathbf{A}$, $\mathbf{B}$ and $\mathbf{C}$. Interpretation of the component matrices depends upon how $\underline{\mathbf{X}}$ was constructed (i.e. which dimension represents the samples). In the case of ChemoSpec2D $\mathbf{C}$ contains values analogous to scores in that they can be used to see how samples cluster (this is because the samples are the third dimension of $\underline{\mathbf{X}}$). Standard matrix multiplication of $\mathbf{A} \ \times \ \mathbf{B^T}$ for a particular column (component) gives a 2D loading plot (a pseudo-spectrum) showing the contributions (loadings) of each peak to the component. ChemoSpec2D uses the R package multiway to carry out PARAFAC (@Helwig2019).

References



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ChemoSpec2D documentation built on March 16, 2021, 9:08 a.m.