fMRI is the preeminent method for collecting signals from the human brain in vivo, for using these signals in the service of functional discovery, and relating these discoveries to anatomical structure. Numerous computational and mathematical techniques have been deployed to extract information from the fMRI signal. Yet, the application of Topological Data Analyses (TDA) remain limited to certain sub-areas such as connectomics (that is, with summarized versions of fMRI data). While connectomics is a natural and important area of application of TDA, applications of TDA in the service of extracting structure from the (non-summarized) fMRI data itself are heretofore nonexistent. “Structure” within fMRI data is determined by dynamic fluctuations in spatially distributed signals over time, and TDA is well positioned to help researchers better characterize mass dynamics of the signal by rigorously capturing shape within it. To accurately motivate this idea, we a) survey an established method in TDA (“persistent homology”) to reveal and describe how complex structures can be extracted from data sets generally, and b) describe how persistent homology can be applied specifically to fMRI data. We provide explanations for some of the mathematical underpinnings of TDA (with expository figures), building ideas in the following sequence: a) fMRI researchers can and should use TDA to extract structure from their data; b) this extraction serves an important role in the endeavor of functional discovery, and c) TDA approaches can complement other established approaches toward fMRI analyses (for which we provide examples). We also provide detailed applications of TDA to fMRI data collected using established paradigms, and offer our software pipeline for readers interested in emulating our methods. This working overview is both an inter-disciplinary synthesis of ideas (to draw researchers in TDA and fMRI toward each other) and a detailed description of methods that can motivate collaborative research.
<p style='text-indent:20px;'>Time-series data are amongst the most widely-used in biomedical sciences, including domains such as functional Magnetic Resonance Imaging (fMRI). Structure within time series data can be captured by the tools of topological data analysis (TDA). Persistent homology is the mostly commonly used data-analytic tool in TDA, and can effectively summarize complex high-dimensional data into an interpretable 2-dimensional representation called a <i>persistence diagram</i>. Existing methods for statistical inference for persistent homology of data depend on an independence assumption being satisfied. While persistent homology can be computed for each time index in a time-series, time-series data often fail to satisfy the independence assumption. This paper develops a statistical test that obviates the independence assumption by implementing a multi-level block sampled Monte Carlo test with sets of persistence diagrams. Its efficacy for detecting task-dependent topological organization is then demonstrated on simulated fMRI data. This new statistical test is therefore suitable for analyzing persistent homology of fMRI data, and of non-independent data in general.</p>
In this study we examined uses of the number 3017 as a neologism by members of an online forum. 3017 has a number of factors working against its success as a neologism, but its use grew dramatically over the course of six years. Statistical analyses showed that the growth data were very well modeled by both a quadratic and a sigmoid curve. The form was used primarily as an adjective and to a lesser extent as a noun over the first 500 days, before verbal forms came to dominate. To understand the structure of the 3017 concept in the mental lexicons of users, we examine attempts to define the term, and disagreements and negotiations about what the term does and does not include. Finally, we include examples of users’ creativity and productivity with the form, including readily-understood jokes.
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