🍩 Database of Original & Non-Theoretical Uses of Topology

(found 8 matches in 0.00182s)

  1. Topological Data Analysis Reveals a Core Gene Expression Backbone That Defines Form and Function Across Flowering Plants (2023)

    Sourabh Palande, Joshua A. M. Kaste, Miles D. Roberts, Kenia Segura Abá, Carly Claucherty, Jamell Dacon, Rei Doko, Thilani B. Jayakody, Hannah R. Jeffery, Nathan Kelly, Andriana Manousidaki, Hannah M. Parks, Emily M. Roggenkamp, Ally M. Schumacher, Jiaxin Yang, Sarah Percival, Jeremy Pardo, Aman Y. Husbands, Arjun Krishnan, Beronda L. Montgomery, Elizabeth Munch, Addie M. Thompson, Alejandra Rougon-Cardoso, Daniel H. Chitwood, Robert VanBuren
    Abstract Since they emerged approximately 125 million years ago, flowering plants have evolved to dominate the terrestrial landscape and survive in the most inhospitable environments on earth. At their core, these adaptations have been shaped by changes in numerous, interconnected pathways and genes that collectively give rise to emergent biological phenomena. Linking gene expression to morphological outcomes remains a grand challenge in biology, and new approaches are needed to begin to address this gap. Here, we implemented topological data analysis (TDA) to summarize the high dimensionality and noisiness of gene expression data using lens functions that delineate plant tissue and stress responses. Using this framework, we created a topological representation of the shape of gene expression across plant evolution, development, and environment for the phylogenetically diverse flowering plants. The TDA-based Mapper graphs form a well-defined gradient of tissues from leaves to seeds, or from healthy to stressed samples, depending on the lens function. This suggests that there are distinct and conserved expression patterns across angiosperms that delineate different tissue types or responses to biotic and abiotic stresses. Genes that correlate with the tissue lens function are enriched in central processes such as photosynthetic, growth and development, housekeeping, or stress responses. Together, our results highlight the power of TDA for analyzing complex biological data and reveal a core expression backbone that defines plant form and function.

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  3. Visualizing Emergent Identity of Assemblages in the Consumer Internet of Things: A Topological Data Analysis Approach (2016)

    Thomas Novak, Donna L. Hoffman
    Abstract The identity of a consumer Internet of Things (IoT) assemblage emerges through a historical process of ongoing interactions among consumers, smart devices, and digital information. Topological Data Analysis (TDA), consistent with mathematical aspects of assemblage theory, is used to visualize the underlying possibility space from which individual IoT assemblages emerge.

  4. Homological Scaffold via Minimal Homology Bases (2021)

    Marco Guerra, Alessandro De Gregorio, Ulderico Fugacci, Giovanni Petri, Francesco Vaccarino
    Abstract The homological scaffold leverages persistent homology to construct a topologically sound summary of a weighted network. However, its crucial dependency on the choice of representative cycles hinders the ability to trace back global features onto individual network components, unless one provides a principled way to make such a choice. In this paper, we apply recent advances in the computation of minimal homology bases to introduce a quasi-canonical version of the scaffold, called minimal, and employ it to analyze data both real and in silico. At the same time, we verify that, statistically, the standard scaffold is a good proxy of the minimal one for sufficiently complex networks.

  5. Coexistence Holes Characterize the Assembly and Disassembly of Multispecies Systems (2021)

    Marco Tulio Angulo, Aaron Kelley, Luis Montejano, Chuliang Song, Serguei Saavedra
    Abstract A central goal of ecological research has been to understand the limits on the maximum number of species that can coexist under given constraints. However, we know little about the assembly and disassembly processes under which a community can reach such a maximum number, or whether this number is in fact attainable in practice. This limitation is partly due to the challenge of performing experimental work and partly due to the lack of a formalism under which one can systematically study such processes. Here, we introduce a formalism based on algebraic topology and homology theory to study the space of species coexistence formed by a given pool of species. We show that this space is characterized by ubiquitous discontinuities that we call coexistence holes (that is, empty spaces surrounded by filled space). Using theoretical and experimental systems, we provide direct evidence showing that these coexistence holes do not occur arbitrarily—their diversity is constrained by the internal structure of species interactions and their frequency can be explained by the external factors acting on these systems. Our work suggests that the assembly and disassembly of ecological systems is a discontinuous process that tends to obey regularities.

  6. Clique Topology Reveals Intrinsic Geometric Structure in Neural Correlations (2015)

    Chad Giusti, Eva Pastalkova, Carina Curto, Vladimir Itskov
    Abstract Detecting structure in neural activity is critical for understanding the function of neural circuits. The coding properties of neurons are typically investigated by correlating their responses to external stimuli. It is not clear, however, if the structure of neural activity can be inferred intrinsically, without a priori knowledge of the relevant stimuli. We introduce a novel method, called clique topology, that detects intrinsic structure in neural activity that is invariant under nonlinear monotone transformations. Using pairwise correlations of neurons in the hippocampus, we demonstrate that our method is capable of detecting geometric structure from neural activity alone, without appealing to external stimuli or receptive fields.Detecting meaningful structure in neural activity and connectivity data is challenging in the presence of hidden nonlinearities, where traditional eigenvalue-based methods may be misleading. We introduce a novel approach to matrix analysis, called clique topology, that extracts features of the data invariant under nonlinear monotone transformations. These features can be used to detect both random and geometric structure, and depend only on the relative ordering of matrix entries. We then analyzed the activity of pyramidal neurons in rat hippocampus, recorded while the animal was exploring a 2D environment, and confirmed that our method is able to detect geometric organization using only the intrinsic pattern of neural correlations. Remarkably, we found similar results during nonspatial behaviors such as wheel running and rapid eye movement (REM) sleep. This suggests that the geometric structure of correlations is shaped by the underlying hippocampal circuits and is not merely a consequence of position coding. We propose that clique topology is a powerful new tool for matrix analysis in biological settings, where the relationship of observed quantities to more meaningful variables is often nonlinear and unknown.

  7. Feasibility of Topological Data Analysis for Event-Related fMRI (2019)

    Cameron T. Ellis, Michael Lesnick, Gregory Henselman-Petrusek, Bryn Keller, Jonathan D. Cohen
    Abstract Recent fMRI research shows that perceptual and cognitive representations are instantiated in high-dimensional multivoxel patterns in the brain. However, the methods for detecting these representations are limited. Topological data analysis (TDA) is a new approach, based on the mathematical field of topology, that can detect unique types of geometric features in patterns of data. Several recent studies have successfully applied TDA to study various forms of neural data; however, to our knowledge, TDA has not been successfully applied to data from event-related fMRI designs. Event-related fMRI is very common but limited in terms of the number of events that can be run within a practical time frame and the effect size that can be expected. Here, we investigate whether persistent homology—a popular TDA tool that identifies topological features in data and quantifies their robustness—can identify known signals given these constraints. We use fmrisim, a Python-based simulator of realistic fMRI data, to assess the plausibility of recovering a simple topological representation under a variety of conditions. Our results suggest that persistent homology can be used under certain circumstances to recover topological structure embedded in realistic fMRI data simulations.How do we represent the world? In cognitive neuroscience it is typical to think representations are points in high-dimensional space. In order to study these kinds of spaces it is necessary to have tools that capture the organization of high-dimensional data. Topological data analysis (TDA) holds promise for detecting unique types of geometric features in patterns of data. Although potentially useful, TDA has not been applied to event-related fMRI data. Here we utilized a popular tool from TDA, persistent homology, to recover topological signals from event-related fMRI data. We simulated realistic fMRI data and explored the parameters under which persistent homology can successfully extract signal. We also provided extensive code and recommendations for how to make the most out of TDA for fMRI analysis.

  8. Using Persistent Homology as a New Approach for Super-Resolution Localization Microscopy Data Analysis and Classification of γH2AX Foci/Clusters (2018)

    Andreas Hofmann, Matthias Krufczik, Dieter W. Heermann, Michael Hausmann
    Abstract DNA double strand breaks (DSB) are the most severe damages in chromatin induced by ionizing radiation. In response to such environmentally determined stress situations, cells have developed repair mechanisms. Although many investigations have contributed to a detailed understanding of repair processes, e.g., homologous recombination repair or non-homologous end-joining, the question is not sufficiently answered, how a cell decides to apply a certain repair process at a certain damage site, since all different repair pathways could simultaneously occur in the same cell nucleus. One of the first processes after DSB induction is phosphorylation of the histone variant H2AX to γH2AX in the given surroundings of the damaged locus. Since the spatial organization of chromatin is not random, it may be conclusive that the spatial organization of γH2AX foci is also not random, and rather, contributes to accessibility of special repair proteins to the damaged site, and thus, to the following repair pathway at this given site. The aim of this article is to demonstrate a new approach to analyze repair foci by their topology in order to obtain a cell independent method of categorization. During the last decade, novel super-resolution fluorescence light microscopic techniques have enabled new insights into genome structure and spatial organization on the nano-scale in the order of 10 nm. One of these techniques is single molecule localization microscopy (SMLM) with which the spatial coordinates of single fluorescence molecules can precisely be determined and density and distance distributions can be calculated. This method is an appropriate tool to quantify complex changes of chromatin and to describe repair foci on the single molecule level. Based on the pointillist information obtained by SMLM from specifically labeled heterochromatin and γH2AX foci reflecting the chromatin morphology and repair foci topology, we have developed a new analytical methodology of foci or foci cluster characterization, respectively, by means of persistence homology. This method allows, for the first time, a cell independent comparison of two point distributions (here the point distributions of two γH2AX clusters) with each other of a selected ensample and to give a mathematical measure of their similarity. In order to demonstrate the feasibility of this approach, cells were irradiated by low LET (linear energy transfer) radiation with different doses and the heterochromatin and γH2AX foci were fluorescently labeled by antibodies for SMLM. By means of our new analysis method, we were able to show that the topology of clusters of γH2AX foci can be categorized depending on the distance to heterochromatin. This method opens up new possibilities to categorize spatial organization of point patterns by parameterization of topological similarity.