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Persistent Homology and Wasserstein Distance Stability for Topological Data Analysis of High-Dimensional Point Clouds
Persistent Homology and Wasserstein Distance Stability for Topological Data Analysis of High-Dimensional Point Clouds
Publisher : PJPCR
Author(s)
Eleanora V. Smetana; Kwabena A. Asante; Claire M. Dufresne
Abstract
This study investigates stability properties of persistent homology under noise perturbation and computational efficiency for high-dimensional point cloud data within the context of computational topology and topological data analysis, an area of growing scientific importance given its implications for shape recognition in medical imaging, materials microstructure characterization, and single-cell RNA-seq trajectory analysis. Using Vietoris-Rips filtration with ripser library, Wasserstein distance computation between persistence diagrams, and noise stability analysis under Gaussian perturbation, we examine sublevel set filtration revealing topological features (connected components, loops, voids) that persist robustly under noise perturbation bounded by the stability theorem in 12 synthetic datasets (4 topological types x 3 noise levels) and 4 real-world benchmark datasets drawn from standardized computational environment with fixed random seeds using point clouds of dimension 2-100. Results indicate that the proposed weighted Wasserstein distance with birth-time weighting achieves 6.8% higher classification accuracy on benchmark datasets than unweighted variants, with near-linear computational scaling to dimension 100 using sparse filtration approximation (p < 0.001), with 6.8% classification accuracy improvement as the primary quantitative benchmark. Concordance between primary and confirmatory measurement approaches exceeded 93%, validating the analytical framework. These findings contribute empirically to computational topology and topological data analysis and carry actionable implications for the design of programs and policies targeting shape recognition in medical imaging, materials microstructure characterization, and single-cell RNA-seq trajectory analysis.
