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A Bayesian Computational Approach to Explore the Optimal Duration of a Cell Proliferation Assay.

Alexander P BrowningScott W McCueMatthew J Simpson
Published in: Bulletin of mathematical biology (2017)
Cell proliferation assays are routinely used to explore how a low-density monolayer of cells grows with time. For a typical cell line with a doubling time of 12 h (or longer), a standard cell proliferation assay conducted over 24 h provides excellent information about the low-density exponential growth rate, but limited information about crowding effects that occur at higher densities. To explore how we can best detect and quantify crowding effects, we present a suite of in silico proliferation assays where cells proliferate according to a generalised logistic growth model. Using approximate Bayesian computation we show that data from a standard cell proliferation assay cannot reliably distinguish between classical logistic growth and more general non-logistic growth models. We then explore, and quantify, the trade-off between increasing the duration of the experiment and the associated decrease in uncertainty in the crowding mechanism.
Keyphrases
  • cell proliferation
  • high throughput
  • induced apoptosis
  • cell cycle
  • pi k akt
  • healthcare
  • endoplasmic reticulum stress
  • big data
  • molecular dynamics simulations
  • deep learning