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PreprintCC BY 4.0arXiv

From Individual Trajectories to Population Densities: Weak-Form Inference of Heterogeneous Growth Laws

Abstract

Single-cell time-lapse microscopy now provides high-resolution size trajectories for thousands of individual cells, yet principled methods for simultaneously learning the functional form of growth laws and the distribution of cell-to-cell physiological variability remain limited. We present a data-driven framework based on the recent Weak-form Estimation of Nonlinear Dynamics (WENDy) algorithm to (i) select the best supported growth law from a set of candidate laws, and (ii) recover individual-level growth parameters via empirical Bayes shrinkage within a random-effects model. We demonstrate the approach on both synthetic individual size data incorporating commonly found growth laws and recorded real size trajectories, showing that the method accurately recovers both growth-law structure and parameter heterogeneity at reasonable noise levels. We finally end with a discussion on how the results obtained by the method here can be upscaled to the population level.

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BibTeX
@misc{lyons2026from,
  title = {{From Individual Trajectories to Population Densities: Weak-Form Inference of Heterogeneous Growth Laws}},
  author = {Rainey Lyons and Vanja Dukic and David M Bortz},
  howpublished = {arXiv},
  year = {2026},
  month = sep,
  doi = {10.48550/arxiv.2609.31955},
  eprint = {2609.31955},
  archivePrefix = {arXiv},
  url = {https://arxiv.org/abs/2609.31955},
  note = {CC BY 4.0},
}
RIS
TY  - UNPB
TI  - From Individual Trajectories to Population Densities: Weak-Form Inference of Heterogeneous Growth Laws
AU  - Rainey Lyons
AU  - Vanja Dukic
AU  - David M Bortz
PY  - 2026
DA  - 2026/09/25
PB  - arXiv
DO  - 10.48550/arxiv.2609.31955
UR  - https://arxiv.org/abs/2609.31955
AB  - Single-cell time-lapse microscopy now provides high-resolution size trajectories for thousands of individual cells, yet principled methods for simultaneously learning the functional form of growth laws and the distribution of cell-to-cell physiological variability remain limited. We present a data-driven framework based on the recent Weak-form Estimation of Nonlinear Dynamics (WENDy) algorithm to (i) select the best supported growth law from a set of candidate laws, and (ii) recover individual-level growth parameters via empirical Bayes shrinkage within a random-effects model. We demonstrate the approach on both synthetic individual size data incorporating commonly found growth laws and recorded real size trajectories, showing that the method accurately recovers both growth-law structure and parameter heterogeneity at reasonable noise levels. We finally end with a discussion on how the results obtained by the method here can be upscaled to the population level.
ER  -