Evidence map›Paper›PMID 30645629›Full record

ArticlePloS one2019

Machine learning framework for assessment of microbial factory performance.

Tolutola Oyetunde, Di Liu, Hector Garcia Martin, Yinjie J Tang

Abstract read
In one paragraph

Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed.

  1. Article
  2. Computational and structural biotechnology journal · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Optimizing Ethanol Production inACS synthetic biology · 2023
    Article
  9. Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Exploring synergies between plant metabolic modelling and machine learning.Computational and structural biotechnology journal · 2022
    Review
  18. Review
  19. Article
  20. The era of big data: Genome-scale modelling meets machine learning.Computational and structural biotechnology journal · 2020
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Tolutola OyetundeDepartment of Energy, Environmental and Chemical Engineering, Washington University, Saint Louis, Missouri, United States of America.ORCID 0000-0002-3875-8613
Di LiuDepartment of Energy, Environmental and Chemical Engineering, Washington University, Saint Louis, Missouri, United States of America.
Hector Garcia MartinDOE Joint BioEnergy Institute, Emeryville, California, United States of America.ORCID 0000-0002-4556-9685
Yinjie J TangDepartment of Energy, Environmental and Chemical Engineering, Washington University, Saint Louis, Missouri, United States of America.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic models can estimate intrinsic product yields for microbial factories, but such frameworks struggle to predict cell performance (including product titer or rate) under suboptimal metabolism and complex bioprocess conditions. On the other hand, machine learning, complementary to metabolic modeling necessitates large amounts of data. Building such a database for metabolic engineering designs requires significant manpower and is prone to human errors and bias. We propose an approach to integrate data-driven methods with genome scale metabolic model for assessment of microbial bio-production (yield, titer and rate). Using engineered E. coli as an example, we manually extracted and curated a data set comprising about 1200 experimentally realized cell factories from ~100 papers. We furthermore augmented the key design features (e.g., genetic modifications and bioprocess variables) extracted from literature with additional features derived from running the genome-scale metabolic model iML1515 simulations with constraints that match the experimental data. Then, data augmentation and ensemble learning (e.g., support vector machines, gradient boosted trees, and neural networks in a stacked regressor model) are employed to alleviate the challenges of sparse, non-standardized, and incomplete data sets, while multiple correspondence analysis/principal component analysis are used to rank influential factors on bio-production. The hybrid framework demonstrates a reasonably high cross-validation accuracy for prediction of E.coli factory performance metrics under presumed bioprocess and pathway conditions (Pearson correlation coefficients between 0.8 and 0.93 on new data not seen by the model).

Indexed as

AlgorithmsMachine LearningModels, BiologicalComputer SimulationDatabases, FactualEscherichia coliMetabolic EngineeringReproducibility of Results

Identifiers

PMID30645629
PMCPMC6333410

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.