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Philibert Courau

Publications and source records attributed to Philibert Courau.

2 recordsLinked to original sources

The gene's-eye view of quantitative genetics

Modelling the evolution of a continuous trait in a biological population is one of the oldest problems in evolutionary biology, which led to the birth of quantitative genetics. With the recent development of GWAS methods, it has become essential to link the evolution of the trait distribution to the underlying evolution of allelic frequencies at many loci, co-contributing to the trait value. The way most articles go about this is to make assumptions on the trait distribution, and use Wright's formula to model how the evolution of the trait translates on each individual locus. Here, we take a gene's eye-view of the system, starting from an explicit finite-loci model with selection, drift, recombination and mutation, in which the trait value is a direct product of the genome. We let the number of loci go to infinity under the assumption of strong recombination, and characterize the limit behavior of a given locus with a McKean-Vlasov SDE and the corresponding Fokker-Planck IPDE. In words, the selection on a typical locus depends on the mean behaviour of the other loci which can be approximated with the law of the focal locus. Results include the independence of two loci and explicit stationary distribution for allelic frequencies at a given locus (under some assumptions on the fitness function).

math.PR

From individual-based epidemic models to McKendrick-von Foerster PDEs: A guide to modeling and inferring COVID-19 dynamics

We present a unifying, tractable approach for studying the spread of viruses causing complex diseases requiring to be modeled using a large number of types (e.g., infective stage, clinical state, risk factor class). We show that recording each infected individual's infection age, i.e., the time elapsed since infection, has three benefits. First, regardless of the number of types, the age distribution of the population can be described by means of a first-order, one-dimensional partial differential equation (PDE) known as the McKendrick-von Foerster equation. The frequency of type $i$ is simply obtained by integrating the probability of being in state $i$ at a given age against the age distribution. This representation induces a simple methodology based on the additional assumption of Poisson sampling to infer and forecast the epidemic. We illustrate this technique using French data from the COVID-19 epidemic. Second, our approach generalizes and simplifies standard compartmental models using high-dimensional systems of ordinary differential equations (ODEs) to account for disease complexity. We show that such models can always be rewritten in our framework, thus, providing a low-dimensional yet equivalent representation of these complex models. Third, beyond the simplicity of the approach, we show that our population model naturally appears as a universal scaling limit of a large class of fully stochastic individual-based epidemic models, where the initial condition of the PDE emerges as the limiting age structure of an exponentially growing population starting from a single individual.

q-bio.PE