Evidence map›Paper›PMID 24987114›Full record

ArticleMolecular systems biology2014

An integrative, multi-scale, genome-wide model reveals the phenotypic landscape of Escherichia coli.

Javier Carrera, Raissa Estrela, Jing Luo, Navneet Rai, Athanasios Tsoukalas, Ilias Tagkopoulos

Abstract read
In one paragraph

Article in Molecular systems biology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing 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

43 citing papers in PubMed.

  1. Review
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  11. Using genome-wide expression compendia to study microorganisms.Computational and structural biotechnology journal · 2022
    Review
  12. Article
  13. Food and waterborne parasitology · 2021
    Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Simultaneous cross-evaluation of heterogeneousScience (New York, N.Y.) · 2020
    Article
  19. Article
  20. Predicting growth rate from gene expression.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
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

6 authors.

Javier CarreraUC Davis Genome Center, University of California, Davis, CA, USA.
Raissa EstrelaDepartment of Molecular and Cell Biology, University of California, Berkeley, CA, USA.
Jing LuoUC Davis Genome Center, University of California, Davis, CA, USA.
Navneet RaiUC Davis Genome Center, University of California, Davis, CA, USA.
Athanasios TsoukalasUC Davis Genome Center, University of California, Davis, CA, USA Department of Computer Science, University of California, Davis, CA, USA.
Ilias TagkopoulosUC Davis Genome Center, University of California, Davis, CA, USA Department of Computer Science, University of California, Davis, CA, USA iliast@ucdavis.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Given the vast behavioral repertoire and biological complexity of even the simplest organisms, accurately predicting phenotypes in novel environments and unveiling their biological organization is a challenging endeavor. Here, we present an integrative modeling methodology that unifies under a common framework the various biological processes and their interactions across multiple layers. We trained this methodology on an extensive normalized compendium for the gram-negative bacterium Escherichia coli, which incorporates gene expression data for genetic and environmental perturbations, transcriptional regulation, signal transduction, and metabolic pathways, as well as growth measurements. Comparison with measured growth and high-throughput data demonstrates the enhanced ability of the integrative model to predict phenotypic outcomes in various environmental and genetic conditions, even in cases where their underlying functions are under-represented in the training set. This work paves the way toward integrative techniques that extract knowledge from a variety of biological data to achieve more than the sum of their parts in the context of prediction, analysis, and redesign of biological systems.

Indexed as

Genome, BacterialAdaptation, PhysiologicalAlgorithmsEscherichia coliGene Regulatory NetworksMetabolic Networks and PathwaysModels, BiologicalPhenotypeStress, PhysiologicalSystems Biologygenome engineeringgenome‐scale modelmodel‐driven experimentationpredictive modeling and integrationsystems and synthetic biology

Identifiers

PMID24987114
PMCPMC4299492

What OpenQuestion holds

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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.