Extremal events dictate population growth rate inference

Recent methods have been developed to map single-cell lineage statistics to population growth. Because population growth selects for exponentially rare phenotypes, these methods inherently depend on sampling large deviations from finite data, which introduces systematic errors. A comprehensive understanding of these errors in the context of finite data remains elusive. To address this gap, we study the error in growth rate estimates across different models. We show that under the usual bias-variance decomposition, the bias can be decomposed into a finite-time bias and nonlinear averaging bias. We demonstrate that finite-time bias, which dominates at short times, can be mitigated by fitting its monotonic behavior. In contrast, at longer times, nonlinear averaging bias becomes the predominant source of error, leading to a phase transition. This transition can be understood through the Random Energy Model, a mean-field model of disordered systems, where a few lineages dominate the estimator. Applying these methods to experimental data demonstrates that correcting for biases in lineage-based approaches yields consistent results for the long-term growth rate across multiple methods and enables the reverse-engineering of dynamic models. This new framework provides a quantitative understanding of growth rate estimators, clarifies the conditions under which they can be effectively applied to finite data, and introduces model-free approaches for studying the connections between physiology and cell growth.

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Publication Details

Journal
PLoS Computational Biology
Published
2026-05-13
DOI
https://doi.org/10.1371/journal.pcbi.1014088
Primary Topic
Evolution and Genetic Dynamics
Type
preprint
Field-Weighted Citation Impact
0.00

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preprint

Extremal events dictate population growth rate inference

Ethan Levien, Trevor GrandPre, Ariel Amir
PLoS Computational Biology
Evolution and Genetic Dynamics
preprint

Extremal events dictate population growth rate inference

Ethan Levien, Trevor GrandPre, Ariel Amir
preprint en

Abstract

Recent methods have been developed to map single-cell lineage statistics to population growth. Because population growth selects for exponentially rare phenotypes, these methods inherently depend on sampling large deviations from finite data, which introduces systematic errors. A comprehensive understanding of these errors in the context of finite data remains elusive. To address this gap, we study the error in growth rate estimates across different models. We show that under the usual bias-variance decomposition, the bias can be decomposed into a finite-time bias and nonlinear averaging bias. We demonstrate that finite-time bias, which dominates at short times, can be mitigated by fitting its monotonic behavior. In contrast, at longer times, nonlinear averaging bias becomes the predominant source of error, leading to a phase transition. This transition can be understood through the Random Energy Model, a mean-field model of disordered systems, where a few lineages dominate the estimator. Applying these methods to experimental data demonstrates that correcting for biases in lineage-based approaches yields consistent results for the long-term growth rate across multiple methods and enables the reverse-engineering of dynamic models. This new framework provides a quantitative understanding of growth rate estimators, clarifies the conditions under which they can be effectively applied to finite data, and introduces model-free approaches for studying the connections between physiology and cell growth.

PLoS Computational BiologyVol. 22(5)
Dartmouth College (US), Northwestern University (US), Princeton University (US), Washington University in St. Louis (US), Weizmann Institute of Science (IL)
National Science Foundation, European Commission, Israel Science Foundation
Openalex Percentile: Top 100%
Evolution and Genetic Dynamics
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Extremal events dictate population growth rate inference — Ethan Levien, Trevor GrandPre, et al. · PLoS Computational Biology (2026) | TGRS Research Map | TGRS