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Why Biological Systems Suddenly Change State: An Intuitive Guide to Freidlin–Wentzell Theory

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  Stochasticity is ubiquitous in biology and neuroscience, manifesting in various forms, including ion channel noise, synaptic variability, gene regulatory fluctuations, noisy population dynamics, and more. Many biological systems spend long periods in a stable “state” and only rarely transition to another state due to noise. For instance, a neuron typically remains inactive but may occasionally trigger a spontaneous spike. Similarly, a gene can switch from the OFF state to the ON state due to rare bursts of transcription factors. Cells can also transition out of metabolic or epigenetic states, populations might shift between different ecological equilibria, and a viral infection can fluctuate between phases of control and uncontrollability. Freidlin–Wentzell theory provides a mathematically rigorous framework to study these phenomena when noise is small but nonzero . It tells you, firstly, h ow likely rare transitions are,    secondly,   h ow fast they occ...
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A Guided Path Through the Large Deviations Series

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  This post serves as a short guide to the four-part series on large deviations and their applications to stochastic processes, biology, and weak-noise dynamical systems. Each article can be read independently, but together they form a coherent narrative that moves from foundational principles to modern applications. 1. Sanov’s Theorem and the Geometry of Rare Events The series begins with an intuitive introduction to Sanov’s theorem , highlighting how empirical distributions deviate from their expected behavior and how the Kullback-Leibler divergence emerges as the natural rate functional. This post lays the conceptual groundwork for understanding rare events in high-dimensional systems. Read the post → 2. Sanov’s Theorem in Living Systems The second article explores how Sanov’s theorem applies to biological and neural systems . Empirical measures, population variability, and rare transitions in gene expression or neural activity are framed through ...
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Sanov’s Theorem and Girsanov Transformations in Diffusion Processes

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  In the context of large deviation theory, it is valuable to explore how  Sanov’s theorem and the Girsanov transformation interact in the context of two fundamental diffusion models: Brownian motion and the Ornstein–Uhlenbeck process. 1. Introduction Sanov’s theorem describes the exponential decay of probabilities associated with atypical empirical distributions of i.i.d. random variables. Girsanov’s theorem, on the other hand, provides a way to modify the drift of a stochastic process by changing the underlying probability measure. Together, they form a natural bridge between empirical deviations and pathwise deviations in diffusion processes. Notation For clarity, we summarize the variables and symbols used throughout this post: \(X_t\) : generic diffusion process. \(B_t\) : Brownian motion with volatility \(\sigma\). \(\sigma\) : diffusion coefficient (scalar or matrix). \(W_t\) : standard Brownian motion under the reference measure...
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Understanding Anaerobic Threshold (VT2) and VO2 Max in Endurance Training

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  Introduction: The Science Behind Ventilatory Thresholds VT1 vs. VT2: Defining Energy Transitions p (Aerobic Threshold) : The transition from lipid metawwwpp (fat-burning) to a mixed metabolism, where both carbohydrates and fats fuel muscle activity. V0T2 (Anaerobic Threshold) : The point where the  shifts to a predominantly carbohydrate-based wmetabolism , leading to rapid lactate waccumpulation and increased reliance on anaerobic energy pathways. www w In p VT1 and VT2 Wwww ewAgep & Sex Younger athletes generally exhibit higher VT2 values , while aging naturally reduces aerobicw capacity. Men tend to have a higher VO2 Max due to greater lung capacity and muscle mass, but women can achieve similar endurance levels through optimized training. Body Composition & Health Status High body fat percentage may reduce VT2 efficiency, as excess weight increases ...
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Owen's Function: A Simple Solution to Complex Problems

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Definition   If you are interested in statistics or probability, you may have encountered the Owen's function , a special function that arises in various applications involving bivariate normal distributions. Let’s explain what Owen's function is, how it is defined and notated, and why it is useful.  The Owen's function is defined as follows: for any real numbers h and a, Owen's function T(h,a) is given by T ( h , a ) = 1 2 π · ∫ 0 a exp ( - h 2 2 · ( 1 ...
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Diagnosing Singular Fits in Linear Mixed Models: Practical Examples, Code, and Alternatives

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  Introduction This post is the practical follow‑up to When Linear Mixed Models Don’t Converge , where I discussed the theoretical reasons why convergence issues often arise in linear mixed models. Here, we move from theory to practice: simulated examples, diagnostic tools, interpretation of singular fits, and practical modeling alternatives. If you haven’t read the first part yet, you may want to start there for the conceptual foundations. Figure. Conceptual map showing how model complexity and available information interact Legend of Figure 1. Green = identifiable models; yellow = risk of singularity; red = non‑identifiable models. A Concrete Example Using R: When a Random-Slope Model Becomes Singular Let’s simulate a simple dataset with only 8 groups and a very small random‑slope variance. This is a classic scenario where the model converges numerically but is statistically non‑identifiable. ```r set.seed(123) n_groups <- 8 n_per_group <- 20 group <- factor(rep(1:n_gro...
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