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LaMont, C.

Publications and source records attributed to LaMont, C..

2 recordsLinked to original sources

Optimal Control and the Dynamics of Ancestral Lineages

In resource-constrained populations, the growth rate of an allele is coupled to the frequency of its competitors. Since these frequencies are unobserved, exact inference of evolutionary parameters demands integrating over the full ensemble of possible frequency histories. This high-dimensional path integral is computationally prohibitive, and standard phylogenetic approaches avoid its evaluation by treating lineages as unconstrained birth-death processes. However, ignoring the carrying capacity comes at a cost: it necessitates an abundance of free parameters to describe simple allelic replicator dynamics and implicitly assumes an incorrect drift model. We propose a new approach by defining the fitness potential ({Psi})-- a dynamical quantity formally equivalent to the logarithm of reproductive value. By exploiting a duality between evolutionary dynamics and stochastic optimal control, we show that {Psi} allows for the analytic marginalization of the unknown population history. This transformation yields a tractable likelihood function that strictly enforces competitive constraints while accounting for the information loss due to genetic drift in finite populations. We demonstrate that this framework enables parsimonious, site-specific inference of selection coefficients from phylogenetic trees. This dual-control framework shows ancestral lineages behave as optimal agents: they do not simply climb local fitness gradients, but "anticipate" future selection by navigating a global landscape of reproductive value.

evolutionary biology↗

Learning the shape of protein micro-environments with a holographic convolutional neural network

Proteins play a central role in biology from immune recognition to brain activity. While major advances in machine learning have improved our ability to predict protein structure from sequence, determining protein function from structure remains a major challenge. Here, we introduce Holographic Convolutional Neural Network (H-CNN) for proteins, which is a physically motivated machine learning approach to model amino acid preferences in protein structures. H-CNN reflects physical interactions in a protein structure and recapitulates the functional information stored in evolutionary data. H-CNN accurately predicts the impact of mutations on protein function, including stability and binding of protein complexes. Our interpretable computational model for protein structure-function maps could guide design of novel proteins with desired function.

biophysics↗