Evidence map›Paper›PMID 42615979›Full record

ArticleBioinformatics (Oxford, England)2026

A data-driven evaluation of optimization techniques in cell culture media.

Ali Parsaee, Miranda Stahn, Arian Amirvaresi, Reza Ovissipour, David Staszak

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Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ali ParsaeeAlberta Machine Intelligence Institute (AMII), Edmonton, AB T6E 4S6, Canada.ORCID 0009-0003-9576-5806
Miranda StahnNew Harvest, Edmonton, AB T6E 1M4, Canada.
Arian AmirvaresiDepartment of Food Science and Technology, Texas A&M University, College Station, TX 77843-2256, United States.
Reza OvissipourDepartment of Food Science and Technology, Texas A&M University, College Station, TX 77843-2256, United States.
David StaszakAlberta Machine Intelligence Institute (AMII), Edmonton, AB T6E 4S6, Canada.

Funding

Amii and New Harvest, Ali Parsaee, Miranda Stahn, and David Staszak
6 · The paper itself

Abstract

motivationOptimizing cell-culture media for cultivated meat and cellular agriculture is both experimentally demanding and expensive. Traditional approaches use Design of Experiments (DOE) to iterate through candidate formulations until a satisfactory medium emerges. Data-driven methods, and in particular Bayesian optimization (BO), can reach higher objective function values (here, titer) with fewer evaluations than classical DOE. Prior comparisons of optimizers on cell-media data have, however, relied largely on computational simulations rather than measured formulations, leaving researchers without evidence-based guidance on which strategy to adopt.

resultsWe introduce two complementary benchmark protocols and apply them to six published cell-culture datasets. In the "Hide-the-Label" protocol each optimizer begins with only a partial view of the data and sequentially reveals hidden formulations, singly or in batches, reproducing the stepwise acquisition of costly laboratory measurements; the "Open Race" instead measures search efficiency of a method under a fixed evaluation budget. Both protocols were run across four generative surrogate classes [Gaussian process (GP), random forest, neural network, and Bayesian neural network], two difficulty regimes, and batch sizes of one to 20. GP-based BO was consistently the most sample-efficient strategy, locating hidden targets in substantially fewer evaluations than classical DOE designs or random search; its advantage narrowed but remained under injected noise and multi-modality, and optimizers built on more complex surrogates (deeper networks or adaptive ensembles) performed worse rather than better on these harder landscapes. We detail the mathematical basis of the benchmark, criteria for selecting suitable datasets, and how to obtain statistically robust conclusions in the presence of measurement bias and heterogeneity, and we provide a roadmap for selecting an optimization strategy in practice. AVAILABILITY AND IMPLEMENTATION: Source code and the benchmark datasets are freely available at https://github.com/Amii-Applied-AI/amii-cell-ag-tools/tree/main/active-learning-for-cell-media and archived at https://doi.org/10.5281/zenodo.21501659.

Indexed as

Cell Culture TechniquesComputational BiologyCulture MediaAlgorithmsBayes TheoremComputer SimulationCulture Media

Identifiers

PMID42615979
PMCPMC13529365

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.