A kernel for multi-parameter persistent homology

Abstract: Neurodegenerative diseases, such as Alzheimer's and Parkinson's, are characterized by progressive neuronal deterioration, leading to cognitive and motor impairments. Early detection is crucial for effective intervention and management. This study proposes a novel framework utilizing Topological Data Analysis (TDA), particularly persistent homology, to identify early biomarkers from neuroimaging and physiological data. This study explores the application of TDA techniques—specifically persistent homology and topological invariants—for the early detection of neurodegenerative diseases such as Alzheimer's. By analyzing functional brain connectivity, gait dynamics, and molecular structures associated with disease progression, the research demonstrates that TDA can capture subtle, yet critical, topological signatures indicative of early neurodegenerative changes. Layer-wise topological complexity in neural networks and persistent homology in clinical datasets reveal distinct structural degradation patterns. The integration of TDA with machine learning models enhances diagnostic accuracy, interpretability, and generalization, offering a promising direction for non-invasive, data-driven diagnostics in neurology.By capturing the intrinsic topological features of brain networks, the framework aims to distinguish between healthy and early-stage neurodegenerative conditions, offering a robust tool for early diagnosis.Topological Data Analysis (TDA) offers a robust mathematical framework for extracting shape-based features from high-dimensional and noisy biomedical data. Keywords: Topological Data Analysis, Persistent Homology, Neurodegenerative Disease, Alzheimer's, Brain Connectivity, Early Diagnosis, Betti Numbers, Gait Analysis, Functional Networks, Machine Learning, Biomedical Data

Topological Data Analysis (TDA) and its mainstay computational device, persistent homology (PH), has established a strong track record of providing researchers across the data-driven sciences with new insights and methodologies by characterizing low-dimensional geometric structures in high-dimensional data. When combined with machine learning (ML) methods, PH is valued as a discriminating-feature extraction tool. This work highlights many of the recent successes at the intersection of TDA and ML, introduces some of the foundational mathematics underpinning TDA, and summarizes the efforts to strengthen the bridge between TDA and ML. Thus, this document is a launching point for experimentalists and theoreticians to consider what can be learned from the shape of their data.

Convolutional Neural Network (CNN) is a powerful and successful deep learning technique for a variety of computer vision and image analysis applications. Interpreting and explaining the decisions of CNNs is one of the most challengeable tasks despite its significant success in various image analysis tasks. Topological Data Analysis (TDA) is an approach that exploits algebraic invariants from topology to analyse high dimensional and noisy datasets as well as growing challenges of big data applications. Persistent homology (PH) is an algebraic topology method for measuring topological features of shapes and/or functions at different distance or similarity resolutions. This work is an attempt to investigate the algebraic properties of pretrained CNN convolutional layer filters based on random Gaussian/Uniform distribution. We shall investigate the stability and sensitivity of the condition number of CNN filters during and post the model training with focus on class discriminability of the PH features of the convolved images. We shall demonstrate a strong link between the condition number of the CNN filters and their discriminating power of the PH representation. In particular, we shall establish that if small perturbation added to the original images then feature maps with well-conditioned filters will produce similar topological features to the original image. Our investigation and findings are based on training CNN's with Digits, MNIST and CIFAR-10 datasets. Our ultimate interest in applying the results of these findings in designing appropriate CNN models for classifications of ultrasound tumor scan images. Preliminary results for these applications are encouraging.

Single-cell technologies have revolutionized our ability to interrogate biological systems at unprecedented resolution, revealing complex cellular heterogeneity and dynamic processes that underlie development, disease, and immune responses. However, the high dimensionality and nonlinear structure of single-cell data present substantial analytical challenges. Topological data analysis offers a powerful mathematical framework for capturing the intrinsic shape of data, providing novel insights that complement and extend traditional statistical and machine learning methods. By leveraging tools such as persistent homology and the Mapper algorithm, TDA enables the detection of subtle, multiscale patterns – including rare cell populations, transitional states, and branching trajectories – that are often obscured by conventional approaches. In this review, we explore the theoretical foundations of topological data analysis and examine its emerging applications across single-cell transcriptomics, proteomics, and spatial biology. We highlight how this approach can unveil previously unrecognized biological phenomena, from alternative differentiation paths to complex tissue architectures, and discuss the growing ecosystem of computational tools that support its use. As single-cell datasets become increasingly large and multimodal, topological data analysis stands out as a uniquely robust and interpretable approach, with the potential to deepen our understanding of cellular identity and function in health and disease. TDA is specially suited for fields such as systems immunology since it can capture the complex, nonlinear structures inherent in high-dimensional immune data helping to identify distinct immune cell states, differentiation pathways, and dynamic responses to infection or therapy. This topological perspective complements traditional statistical approaches, providing a robust, scale-invariant framework for uncovering hidden organization within the immune system’s complexity.

Topological methods are very rarely used in structural health monitoring (SHM), or indeed in structural dynamics generally, especially when considering the structure and topology of observed data. Topological methods can provide a way of proposing new metrics and methods of scrutinising data, that otherwise may be overlooked. In this work, a method of quantifying the shape of data, via a topic called topological data analysis will be introduced. The main tool within topological data analysis is persistent homology. Persistent homology is a method of quantifying the shape of data over a range of length scales. The required background and a method of computing persistent homology is briefly introduced here. Ideas from topological data analysis are applied to a Z24 Bridge case study, to scrutinise different data partitions, classified by the conditions at which the data were collected. A metric, from topological data analysis, is used to compare between the partitions. The results presented demonstrate that the presence of damage alters the manifold shape more significantly than the effects present from temperature.

Topological data analysis is an emerging area in exploratory data analysis and data mining. Its main tool, persistent homology, has become a popular technique to study the structure of complex, high-dimensional data. In this paper, we propose a novel method using persistent homology to quantify structural changes in time-varying graphs. Specifically, we transform each instance of the time-varying graph into a metric space, extract topological features using persistent homology, and compare those features over time. We provide a visualization that assists in time-varying graph exploration and helps to identify patterns of behavior within the data. To validate our approach, we conduct several case studies on real-world datasets and show how our method can find cyclic patterns, deviations from those patterns, and one-time events in time-varying graphs. We also examine whether a persistence-based similarity measure satisfies a set of well-established, desirable properties for graph metrics.

BackgroundAttention-deficit/hyperactivity disorder (ADHD) is currently diagnosed by a diagnostic interview, mainly based on subjective reports from parents or teachers. It is necessary to develop methods that rely on objectively measureable neurobiological data to assess brain-behavior relationship in patients with ADHD. We investigated the application of a topological data analysis tool, Mapper, to analyze the brain functional connectivity data from ADHD patients.MethodsTo quantify the disease severity using the neuroimaging data, the decomposition of individual functional networks into normal and disease components by the healthy state model (HSM) was performed, and the magnitude of the disease component (MDC) was computed. Topological data analysis using Mapper was performed to distinguish children with ADHD (n = 196) from typically developing controls (TDC) (n = 214).ResultsIn the topological data analysis, the partial clustering results of patients with ADHD and normal subjects were shown in a chain-like graph. In the correlation analysis, the MDC showed a significant increase with lower intelligence scores in TDC. We also found that the rates of comorbidity in ADHD significantly increased when the deviation of the functional connectivity from HSM was large. In addition, a significant correlation between ADHD symptom severity and MDC was found in part of the dataset.ConclusionsThe application of HSM and topological data analysis methods in assessing the brain functional connectivity seem to be promising tools to quantify ADHD symptom severity and to reveal the hidden relationship between clinical phenotypic variables and brain connectivity.

Asthma is a complex respiratory disease characterised by spatial ventilation heterogeneity (VH) in the lung. Multiple breath washout (MBW) and forced oscillation technique (FOT) testing has been shown to quantify VH at the mouth. Methods to provide fresh insight into the mechanisms driving VH are urgently needed to support treatment development. Computed tomography (CT) with parametric response map (PRM) analysis provides spatial and functional lung data. Integrated data sets of imaging features and VH markers present the problem of extracting meaningful information from high dimensional objects; topological data analysis (TDA) has demonstrated recent success in solving this problem. In this thesis topological methods are applied to extract information about lung anatomy and function from imaging data to study association with VH in innately high dimensional integrated data sets. It was sought to describe the spatial distributions of voxel based metrics, visualise the lungs using TDA methods, and combine PRM with simulated airway tree models to improve computational modelling of FOT. Data was obtained from a clinical trial involving 52 subjects, 41 asthmatic (11 healthy). An algorithm was developed to quantify directional Hounsfield unit change (ΔHU) gradients. TDA was applied to integrated data sets and voxel sets with measures of airway tree depth. FOT modelling was augmented with ΔHU about simulated acinar airways.Inferior-to-superior ΔHU gradient best differentiated VH markers. Visualisations of the lungs illustrated gradient reversal and increased heterogeneity in ΔHU in asthmatics. FOT modelling using ΔHU parameterisation showed increased correlation between clinically measured and simulated FOT small airway resistance (R5-R20). In this thesis additional insight is presented into mechanisms affecting VH markers derived from MBW and FOT. Topological methods to analyse imaging data were developed and implemented, including workflows to visualise the lungs and lung function. Linking simulated airway tree geometry with ΔHU showed improvement in FOT modelling.

Persistent homology is a powerful tool in topological data analysis (TDA) to compute, study and encode efficiently multi-scale topological features and is being increasingly used in digital image classification. The topological features represent number of connected components, cycles, and voids that describe the shape of data. Persistent homology extracts the birth and death of these topological features through a filtration process. The lifespan of these features can represented using persistent diagrams (topological signatures). Cubical homology is a more efficient method for extracting topological features from a 2D image and uses a collection of cubes to compute the homology, which fits the digital image structure of grids. In this research, we propose a cubical homology-based algorithm for extracting topological features from 2D images to generate their topological signatures. Additionally, we propose a score, which measures the significance of each of the sub-simplices in terms of persistence. Also, gray level co-occurrence matrix (GLCM) and contrast limited adapting histogram equalization (CLAHE) are used as a supplementary method for extracting features. Machine learning techniques are then employed to classify images using the topological signatures. Among the eight tested algorithms with six published image datasets with varying pixel sizes, classes, and distributions, our experiments demonstrate that cubical homology-based machine learning with deep residual network (ResNet 1D) and Light Gradient Boosting Machine (lightGBM) shows promise with the extracted topological features.

Topological Data Analysis is a set of mathematical methods for capturing the structure of data forms. TDA has been used to cope with noisy signals and time series. TDA is used to discover the key characteristics of data, which are shapes. One of the basic techniques for TDA is persistent homology which is used to do a study of time series and signal processing. Human activity analysis is a well-researched issue in the field of vision, with large research on the topic. The produced time- series data is typically high-dimensional, intrinsic, non-linear, and non-stationary, leading to pattern changes. The data acquired by a person’s numerous sensors, as well as their placement and orientation, often produces noisy and complicated data, resulting in poor model performance. The implementation method must be data-driven, independent of sensor location and orientation, and employ a coordinate and parameter-free strategy to identify the variable time series data. We need technology that can represent a low-dimensional manifold compactly, identify emergent behaviors, and globalize the system. The persistent homology having property being co- ordinate free. Sensor placement has little effect on time series factorization using persistent homology. This paper gives an overview of topological approaches as well as the problems of human activity analysis, as well as recommendations for the future.

Cytometry experiments yield high-dimensional point cloud data that is difficult to interpret manually. Boolean gating techniques coupled with comparisons of relative abundances of cellular subsets is the current standard for cytometry data analysis. However, this approach is unable to capture more subtle topological features hidden in data, especially if those features are further masked by data transforms or significant batch effects or donor-to-donor variations in clinical data. We present that persistent homology, a mathematical structure that summarizes the topological features, can distinguish different sources of data, such as from groups of healthy donors or patients, effectively. Analysis of publicly available cytometry data describing non-naïve CD8+ T cells in COVID-19 patients and healthy controls shows that systematic structural differences exist between single cell protein expressions in COVID-19 patients and healthy controls. We identify proteins of interest by a decision-tree based classifier, sample points randomly and compute persistence diagrams from these sampled points. The resulting persistence diagrams identify regions in cytometry datasets of varying density and identify protruded structures such as ‘elbows’. We compute Wasserstein distances between these persistence diagrams for random pairs of healthy controls and COVID-19 patients and find that systematic structural differences exist between COVID-19 patients and healthy controls in the expression data for T-bet, Eomes, and Ki-67. Further analysis shows that expression of T-bet and Eomes are significantly downregulated in COVID-19 patient non-naïve CD8+ T cells compared to healthy controls. This counter-intuitive finding may indicate that canonical effector CD8+ T cells are less prevalent in COVID-19 patients than healthy controls. This method is applicable to any cytometry dataset for discovering novel insights through topological data analysis which may be difficult to ascertain otherwise with a standard gating strategy or existing bioinformatic tools.

Abstract: Sparse and high-dimensional data present persistent challenges in artificial intelligence (AI), particularly in maintaining generalizability, interpretability, and computational efficiency. This study proposes a unified advanced framework that integrates tensor algebra, number theory, topology, and analytic geometry to address the limitations of traditional machine learning models when handling sparse data. The methodology leverages high-order tensor representations for compact and expressive encoding of multi-dimensional information, modular arithmetic for robust and secure feature embedding, and persistent homology to capture topological invariants within data distributions. Additionally, geometric learning principles based on Riemannian manifolds are incorporated to guide optimization processes through curvature-aware gradient flows. The proposed framework is further enhanced by quantum computational principles, where tensor networks and entangled state representations are simulated for efficient processing. Experimental evaluation on classical and quantum datasets demonstrates superior performance in terms of accuracy, F1 score, and convergence rate when compared to baseline and modular AI architectures. The results validate that the integration of mathematical rigor and quantum principles can offer scalable, interpretable, and resilient solutions for sparse data modeling. This framework not only contributes to the theoretical foundation of AI and quantum learning but also provides practical implications for applications in cryptography, biomedical analysis, and high-dimensional signal processing. Keywords Sparse data modeling, tensor algebra, quantum machine learning, topological data analysis, modular arithmetic, Riemannian geometry, tensor networks, persistent homology, quantum-enhanced AI, high-dimensional data

BOLD-based fMRI is the most widely used method for studying brain function. The BOLD signal while valuable, is beset with unique vulnerabilities. The most notable of these is the modest signal to noise ratio, and the relatively low temporal and spatial resolution. However, the high dimensional complexity of the BOLD signal also presents unique opportunities for functional discovery. Topological Data Analyses (TDA), a branch of mathematics optimized to search for specific classes of structure within high dimensional data may provide particularly valuable applications. In this investigation, we acquired fMRI data in the anterior cingulate cortex (ACC) using a basic motor control paradigm. Then, for each participant and each of three task conditions, fMRI signals in the ACC were summarized using two methods: a) TDA based methods of persistent homology and persistence landscapes and b) non-TDA based methods using a standard vectorization scheme. Finally, using machine learning (with support vector classifiers), classification accuracy of TDA and non-TDA vectorized data was tested across participants. In each participant, TDA-based classification out-performed the non-TDA based counterpart, suggesting that our TDA analytic pipeline better characterized task- and condition-induced structure in fMRI data in the ACC. Our results emphasize the value of TDA in characterizing task- and condition-induced structure in regional fMRI signals. In addition to providing our analytical tools for other users to emulate, we also discuss the unique role that TDA-based methods can play in the study of individual differences in the structure of functional brain signals in the healthy and the clinical brain.

In topological data analysis, persistent homology is used to study the ‘shape of data’. Persistent homology computations are completely characterized by a set of intervals called a bar code. It is often said that the long intervals represent the ‘topological signal’ and the short intervals represent ‘noise’. We give evidence to dispute this thesis, showing that the short intervals encode geometric information. Specifically, we prove that persistent homology detects the curvature of disks from which points have been sampled. We describe a general computational framework for solving inverse problems using the average persistence landscape, a continuous mapping from metric spaces with a probability measure to a Hilbert space. In the present application, the average persistence landscapes of points sampled from disks of constant curvature results in a path in this Hilbert space which may be learned using standard tools from statistical and machine learning.

Persistent homology is a fundamental tool in topological data analysis used for the most diverse applications. Information captured by persistent homology is commonly visualized using scatter plots representations. Despite being widely adopted, such a visualization technique limits user understanding and is prone to misinterpretation. This article proposes a new approach for the efficient computation of persistence cycles, a geometric representation of the features captured by persistent homology. We illustrate the importance of rendering persistence cycles when analyzing scalar fields, and we discuss the advantages that our approach provides compared to other techniques in topology-based visualization. We provide an efficient implementation of our approach based on discrete Morse theory, as a new module for the Topology Toolkit. We show that our implementation has comparable performance with respect to state-of-the-art toolboxes while providing a better framework for visually analyzing persistent homology information.