Evidence map›Paper›PMID 28109249›Full record

ArticleBMC bioinformatics2017

Parameter estimation in large-scale systems biology models: a parallel and self-adaptive cooperative strategy.

David R Penas, Patricia González, Jose A Egea, Ramón Doallo, Julio R Banga

Abstract read
In one paragraph

Article in BMC bioinformatics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Trial
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  8. A protocol for dynamic model calibration.Briefings in bioinformatics · 2022
    Article
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  19. Emerging whole-cell modeling principles and methods.Current opinion in biotechnology · 2018
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  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

5 authors.

David R PenasBioProcess Engineering Group, IIM-CSIC, Eduardo Cabello 6, Vigo, 36208, Spain.
Patricia GonzálezComputer Architecture Group, Universidade da Coruña, Campus de Elviña s/n, Coruña, 15071 A, Spain.
Jose A EgeaDepartment of Applied Mathematics and Statistics, Universidad Politécnica de Cartagena, c/ Dr. Fleming s/n, Cartagena, 30202, Spain.
Ramón DoalloComputer Architecture Group, Universidade da Coruña, Campus de Elviña s/n, Coruña, 15071 A, Spain.
Julio R BangaBioProcess Engineering Group, IIM-CSIC, Eduardo Cabello 6, Vigo, 36208, Spain. julio@iim.csic.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe development of large-scale kinetic models is one of the current key issues in computational systems biology and bioinformatics. Here we consider the problem of parameter estimation in nonlinear dynamic models. Global optimization methods can be used to solve this type of problems but the associated computational cost is very large. Moreover, many of these methods need the tuning of a number of adjustable search parameters, requiring a number of initial exploratory runs and therefore further increasing the computation times. Here we present a novel parallel method, self-adaptive cooperative enhanced scatter search (saCeSS), to accelerate the solution of this class of problems. The method is based on the scatter search optimization metaheuristic and incorporates several key new mechanisms: (i) asynchronous cooperation between parallel processes, (ii) coarse and fine-grained parallelism, and (iii) self-tuning strategies.

resultsThe performance and robustness of saCeSS is illustrated by solving a set of challenging parameter estimation problems, including medium and large-scale kinetic models of the bacterium E. coli, bakerés yeast S. cerevisiae, the vinegar fly D. melanogaster, Chinese Hamster Ovary cells, and a generic signal transduction network. The results consistently show that saCeSS is a robust and efficient method, allowing very significant reduction of computation times with respect to several previous state of the art methods (from days to minutes, in several cases) even when only a small number of processors is used.

conclusionsThe new parallel cooperative method presented here allows the solution of medium and large scale parameter estimation problems in reasonable computation times and with small hardware requirements. Further, the method includes self-tuning mechanisms which facilitate its use by non-experts. We believe that this new method can play a key role in the development of large-scale and even whole-cell dynamic models.

Indexed as

AnimalsCHO CellsComputational BiologyCricetulusDrosophila melanogasterEscherichia coliGene Expression RegulationModels, TheoreticalNonlinear DynamicsSaccharomyces cerevisiaeSignal TransductionSystems BiologyTranscription, GeneticDynamic modelsGlobal optimizationMetaheuristicsParallelizationParameter estimation

Identifiers

PMID28109249
PMCPMC5251293

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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.