arXiv subjects

Lydia Robert

Publications and source records attributed to Lydia Robert.

4 recordsLinked to original sources

arXiv2019

Estimating the division rate from indirect measurements of single cells

Is it possible to estimate the dependence of a growing and dividing population on a given trait in the case where this trait is not directly accessible by experimental measurements, but making use of measurements of another variable? This article adresses this general question for a very recent and popular model describing bacterial growth, the so-called incremental or adder model. In this model, the division rate depends on the increment of size between birth and division, whereas the most accessible trait is the size itself. We prove that estimating the division 10 rate from size measurements is possible, we state a reconstruction formula in a deterministic and then in a statistical setting, and solve numerically the problem on simulated and experimental data. Though this represents a severely ill-posed inverse problem, our numerical results prove to be satisfactory.

math.ST↗

arXiv2015

Investigation of asymmetry in E. coli growth rate

The data we analyze derives from the observation of numerous cells of the bacterium Escherichia coli (E. coli) growing and dividing. Single cells grow and divide to give birth to two daughter cells, that in turn grow and divide. Thus, a colony of cells from a single ancestor is structured as a binary genealogical tree. At each node the measured data is the growth rate of the bacterium. In this paper, we study two different data sets. One set corresponds to small complete trees, whereas the other one corresponds to long specific sub-trees. Our aim is to compare both sets. This paper is accessible to post graduate students and readers with advanced knowledge in statistics.

stat.AP↗

arXiv2014

Single-cell analysis of growth in budding yeast and bacteria reveals a common size regulation strategy

To maintain a constant cell size, dividing cells have to coordinate cell cycle events with cell growth. This coordination has for long been supposed to rely on the existence of size thresholds determining cell cycle progression [1]. In budding yeast, size is controlled at the G1/S transition [11]. In agreement with this hypothesis, the size at birth influences the time spent in G1: smaller cells have a longer G1 period [3]. Nevertheless, even though cells born smaller have a longer G1, the compensation is imperfect and they still bud at smaller cell sizes. In bacteria, several recent studies have shown that the incremental model of size control, in which size is controlled by addition of a constant volume (in contrast to a size threshold), is able to quantitatively explain the experimental data on 4 different bacterial species [6, 5, 6, 7]. Here, we report on experimental results for the budding yeast Saccharomyces cerevisiae, finding, surprisingly, that cell size control in this organism is very well described by the incremental model, suggesting a common strategy for cell size control with bacteria. Additionally, we argue that for S. cerevisiae the volume increment is not added from birth to division, but rather between two budding events.

q-bio.CB↗

arXiv2012

Statistical estimation of a growth-fragmentation model observed on a genealogical tree

We model the growth of a cell population by a piecewise deterministic Markov branching tree. Each cell splits into two offsprings at a division rate $B(x)$ that depends on its size $x$. The size of each cell grows exponentially in time, at a rate that varies for each individual. We show that the mean empirical measure of the model satisfies a growth-fragmentation type equation if structured in both size and growth rate as state variables. We construct a nonparametric estimator of the division rate $B(x)$ based on the observation of the population over different sampling schemes of size $n$ on the genealogical tree. Our estimator nearly achieves the rate $n^{-s/(2s+1)}$ in squared-loss error asymptotically. When the growth rate is assumed to be identical for every cell, we retrieve the classical growth-fragmentation model and our estimator improves on the rate $n^{-s/(2s+3)}$ obtained in \cite{DHRR, DPZ} through indirect observation schemes. Our method is consistently tested numerically and implemented on {\it Escherichia coli} data.

math.PR↗