Evidence map›Paper›PMID 27659412›Full record

ArticleBMC bioinformatics2016

solveME: fast and reliable solution of nonlinear ME models.

Laurence Yang, Ding Ma, Ali Ebrahim, Colton J Lloyd, Michael A Saunders, Bernhard O Palsson

Abstract read
In one paragraph

Article in BMC bioinformatics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. A systems-level atlas of carbon-response transcriptional states inProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. Article
  3. Article
  4. Integration of proteomic data with genome-scale metabolic models: A methodological overview.Protein science : a publication of the Protein Society · 2024
    Review
  5. Review
  6. Article
  7. Review
  8. Review
  9. Article
  10. Emergence of diauxie as an optimal growth strategy under resource allocation constraints in cellular metabolism.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Article
  12. Kinetic profiling of metabolic specialists demonstrates stability and consistency of in vivo enzyme turnover numbers.Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  13. Review
  14. Article
  15. Cellular responses to reactive oxygen species are predicted from molecular mechanisms.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors.

Laurence YangDepartment of Bioengineering, University of California at San Diego, La Jolla, 92093, CA, USA.
Ding MaDepartment of Management Science and Engineering, Stanford University, Stanford, 94305, CA, USA.
Ali EbrahimDepartment of Bioengineering, University of California at San Diego, La Jolla, 92093, CA, USA.
Colton J LloydDepartment of Bioengineering, University of California at San Diego, La Jolla, 92093, CA, USA.
Michael A SaundersDepartment of Management Science and Engineering, Stanford University, Stanford, 94305, CA, USA.
Bernhard O PalssonDepartment of Bioengineering, University of California at San Diego, La Jolla, 92093, CA, USA. palsson@ucsd.edu.

Funding

GENOMICALLY BASED MODELS FOR ANTIBIOTIC DEVELOPMENTR01GM057089 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PALSSON, BERNHARD O · 1998 to 2021
$6.9M
Multiscale Molecular Systems Biology: Reconstruction and Model OptimizationU01GM102098 · NIGMS · STANFORD UNIVERSITY · PI SAUNDERS, MICHAEL ALAN · 2012 to 2016
$1.8M
NIGMS NIH HHS R01 GM057089NIGMS NIH HHS U01 GM102098
6 · The paper itself

Abstract

backgroundGenome-scale models of metabolism and macromolecular expression (ME) significantly expand the scope and predictive capabilities of constraint-based modeling. ME models present considerable computational challenges: they are much (>30 times) larger than corresponding metabolic reconstructions (M models), are multiscale, and growth maximization is a nonlinear programming (NLP) problem, mainly due to macromolecule dilution constraints.

resultsHere, we address these computational challenges. We develop a fast and numerically reliable solution method for growth maximization in ME models using a quad-precision NLP solver (Quad MINOS). Our method was up to 45 % faster than binary search for six significant digits in growth rate. We also develop a fast, quad-precision flux variability analysis that is accelerated (up to 60× speedup) via solver warm-starts. Finally, we employ the tools developed to investigate growth-coupled succinate overproduction, accounting for proteome constraints.

conclusionsJust as genome-scale metabolic reconstructions have become an invaluable tool for computational and systems biologists, we anticipate that these fast and numerically reliable ME solution methods will accelerate the wide-spread adoption of ME models for researchers in these fields.

Indexed as

Constraint-based modelingMetabolismNonlinear optimizationProteomeQuasiconvex

Identifiers

PMID27659412
PMCPMC5034503

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.