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PyEcoLib: a python library for simulating stochastic cell size dynamics. | LitMetric

PyEcoLib: a python library for simulating stochastic cell size dynamics.

Phys Biol

Department of Physics. Universidad de los Andes, Bogotá, Colombia.

Published: June 2023

AI Article Synopsis

  • There is a growing demand for simulation tools to understand cell size regulation, which is crucial for studying cell proliferation and gene expression.
  • This article introduces a Python-based library that simulates the random dynamics of bacterial cell size, supporting various parameters such as initial cell size, growth rate, and division strategies.
  • The library helps in analyzing the relationship between cell size dynamics and gene expression, notably how fluctuations in division timing and growth rates affect protein levels, making it easier to incorporate cell size variations into complex gene expression models.

Article Abstract

Recently, there has been an increasing need for tools to simulate cell size regulation due to important applications in cell proliferation and gene expression. However, implementing the simulation usually presents some difficulties, as the division has a cycle-dependent occurrence rate. In this article, we gather a recent theoretical framework in, a python-based library to simulate the stochastic dynamics of the size of bacterial cells. This library can simulate cell size trajectories with an arbitrarily small sampling period. In addition, this simulator can include stochastic variables, such as the cell size at the beginning of the experiment, the cycle duration timing, the growth rate, and the splitting position. Furthermore, from a population perspective, the user can choose between tracking a single lineage or all cells in a colony. They can also simulate the most common division strategies (adder, timer, and sizer) using the division rate formalism and numerical methods. As an example of PyecoLib applications, we explain how to couple size dynamics with gene expression predicting, from simulations, how the noise in protein levels increases by increasing the noise in division timing, the noise in growth rate and the noise in cell splitting position. The simplicity of this library and its transparency about the underlying theoretical framework yield the inclusion of cell size stochasticity in complex models of gene expression.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10665115PMC
http://dx.doi.org/10.1088/1478-3975/acd897DOI Listing

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