Topological Data Analysis: Developments and Applications

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

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 data analysis and its main method, persistent homology, provide a toolkit for computing topological information of high-dimensional and noisy data sets. Kernels for one-parameter persistent homology have been established to connect persistent homology with machine learning techniques with applicability on shape analysis, recognition and classification. We contribute a kernel construction for multi-parameter persistence by integrating a one-parameter kernel weighted along straight lines. We prove that our kernel is stable and efficiently computable, which establishes a theoretical connection between topological data analysis and machine learning for multivariate data analysis.

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.

An Artificial Intelligence Ultrasound Platform for Screening and Staging of Thyroid Cancer

Persistent homology (PH) is a robust method to compute multi-dimensional geometric and topological features of a dataset. Because these features are often stable under certain perturbations of the underlying data, are often discriminating, and can be used for visualization of structure in high-dimensional data and in statistical and machine learning modeling, PH has attracted the interest of researchers across scientific disciplines and in many industry applications. However, computational costs may present challenges to effectively using PH in certain data contexts, and theoretical stability results may not hold in practice. In this paper, we define, implement, and investigate a simplicial complex construction for computing persistent homology of Euclidean point cloud data, which we call the Delaunay-Rips complex (DR). By only considering simplices that appear in the Delaunay triangulation of the point cloud and assigning the Vietoris-Rips weights to simplices, DR avoids potentially costly computations in the persistence calculations. We document and compare a Python implementation of DR with other simplicial complex constructions for generating persistence diagrams. By imposing sufficient conditions on point cloud data, we are able to theoretically justify the stability of the persistence diagrams produced using DR. When the Delaunay triangulation of the point cloud changes under perturbations of the points, we prove that DR-produced persistence diagrams exhibit instability. Since we cannot guarantee that real-world data will satisfy our stability conditions, we demonstrate the practical robustness of DR for persistent homology in comparison with other simplicial complexes in machine learning applications. We find in our experiments that using DR in an ML-TDA pipeline performs comparatively well as using other simplicial complex constructions.

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.

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.

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

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.

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.

Topological Data Analysis is a machine learning method that summarizes the topological features of a space. Persistent Homology (PH) can identify these topological features as they persist within a point cloud; persisting in respect to the connectedness of the point cloud at increasing distances. The utility of PH is apparent in several fields including bioinformatics, network security, and object classification. However, the memory complexity of PH limits the application to relatively small point clouds for low-dimensional topological feature identification. For this reason, numerous approaches to optimize and approximate the PH have been introduced for providing results over large point clouds. One solution, Partitioned Persistent Homology (PPH), has shown favorable approximation on a single node with significant performance improvement. However, the single-node approach is limited by the available system memory, leading to the need for a distributed approach for additional (especially memory) resources. This paper studies a distributed version of PPH for use with large point clouds over a high-performance compute cluster. Experimental results of the distributed algorithm against previous studies is presented along with scalability of the distributed library.

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.

During the past decade, it has been quite successful to observe how computational topology has incorporated some of the fundamental concepts and ideas from algebraic and differential topology into applications. This fusion of theories gave birth to a new field named Topological Data Analysis (TDA), which has a significant value in various fields, ranging from computational biology to personalized medicine and dynamic data analysis. Going beyond its foundational applications, TDA has enriched and complemented classical machine and deep learning frameworks in establishing what is now known as “topological machine learning.” In this paper, we review the present landscape of this emerging field, emphasizing how it merges with machine learning algorithms such as deep neural networks. Each method confers special advantages, targeting areas like machine learning integration, network reconstruction, classification of network regimes, or reduction of noisy data. We described common methodologies, discussed current implementations, and anticipate future challenges in topological machine learning.

BackgroundInterpretation of high-throughput gene expression data continues to require mathematical tools in data analysis that recognizes the shape of the data in high dimensions. Topological data analysis (TDA) has recently been successful in extracting robust features in several applications dealing with high dimensional constructs. In this work, we utilize some recent developments in TDA to curate gene expression data. Our work differs from the predecessors in two aspects: (1) Traditional TDA pipelines use topological signatures called barcodes to enhance feature vectors which are used for classification. In contrast, this work involves curating relevant features to obtain somewhat better representatives with the help of TDA. This representatives of the entire data facilitates better comprehension of the phenotype labels. (2) Most of the earlier works employ barcodes obtained using topological summaries as fingerprints for the data. Even though they are stable signatures, there exists no direct mapping between the data and said barcodes.ResultsThe topology relevant curated data that we obtain provides an improvement in shallow learning as well as deep learning based supervised classifications. We further show that the representative cycles we compute have an unsupervised inclination towards phenotype labels. This work thus shows that topological signatures are able to comprehend gene expression levels and classify cohorts accordingly.ConclusionsIn this work, we engender representative persistent cycles to discern the gene expression data. These cycles allow us to directly procure genes entailed in similar processes.