Frequency-domain alignment of heterogeneous, multidimensional separations data through complex orthogonal Procrustes analysis

TL;DR

This paper introduces a frequency-domain orthogonal Procrustes analysis method to align heterogeneous multidimensional separation data, effectively addressing peak drift issues in complex biological sample analysis.

Contribution

It presents a novel, simple frequency-domain alignment technique using complex orthogonal Procrustes analysis for multidimensional separations data.

Findings

Effective alignment of synthetic chromatograms under challenging scenarios.

Preserves data topology while correcting for shifts.

Applicable to heterogeneous, multidimensional data sets.

Abstract

Multidimensional separations data have the capacity to reveal detailed information about complex biological samples. However, data analysis has been an ongoing challenge in the area since the peaks that represent chemical factors may drift over the course of several analytical runs along the first and second dimension retention times. This makes higher-level analyses of the data difficult, since a 1-1 comparison of samples is seldom possible without sophisticated pre-processing routines. Further complicating the issue is the fact that closely co-eluting components will need to be resolved, typically using some variants of Parallel Factor Analysis (PARAFAC), Multivariate Curve Resolution (MCR), or the recently explored Shift-Invariant Multi-linearity. These algorithms work with a user-specified number of components, and regions of interest that are then summarized as a peak table that is invariant to shift. However, identifying regions of interest across truly heterogeneous data remains an ongoing issue, for automated deployment of these algorithms. This work offers a very simple solution to the alignment problem through a orthogonal Procrustes analysis of the frequency-domain representation of synthetic multidimensional separations data, for peaks that are logarithmically transformed to simulate shift while preserving the underlying topology of the data. Using this very simple method for analysis, two synthetic chromatograms can be compared under close to the worst possible scenarios for alignment.