Evidence map›Paper›PMID 30759197›Full record

ArticleBioinformatics (Oxford, England)2019

Gsmodutils: a python based framework for test-driven genome scale metabolic model development.

James Gilbert, Nicole Pearcy, Rupert Norman, Thomas Millat, Klaus Winzer, John King, Charlie Hodgman, Nigel Minton, Jamie Twycross

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Publishing reproducible dynamic kinetic models.Briefings in bioinformatics · 2021
    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

9 authors.

James GilbertSynthetic Biology Research Centre, University of Nottingham, Nottingham, UK.
Nicole PearcySynthetic Biology Research Centre, University of Nottingham, Nottingham, UK.
Rupert NormanSynthetic Biology Research Centre, University of Nottingham, Nottingham, UK.
Thomas MillatSynthetic Biology Research Centre, University of Nottingham, Nottingham, UK.
Klaus WinzerSynthetic Biology Research Centre, University of Nottingham, Nottingham, UK.
John KingSchool of Mathematical Sciences, University of Nottingham, Nottingham, UK.
Charlie HodgmanSynthetic Biology Research Centre, University of Nottingham, Nottingham, UK.
Nigel MintonSynthetic Biology Research Centre, University of Nottingham, Nottingham, UK.
Jamie TwycrossSchool of Computer Science, University of Nottingham, Nottingham, UK.

Funding

Biotechnology and Biological Sciences Research Council BB/K00283X/1Biotechnology and Biological Sciences Research Council BB/L013940/1Biotechnology and Biological Sciences Research Council BB/L502030/1
6 · The paper itself

Abstract

motivationGenome scale metabolic models (GSMMs) are increasingly important for systems biology and metabolic engineering research as they are capable of simulating complex steady-state behaviour. Constraints based models of this form can include thousands of reactions and metabolites, with many crucial pathways that only become activated in specific simulation settings. However, despite their widespread use, power and the availability of tools to aid with the construction and analysis of large scale models, little methodology is suggested for their continued management. For example, when genome annotations are updated or new understanding regarding behaviour is discovered, models often need to be altered to reflect this. This is quickly becoming an issue for industrial systems and synthetic biotechnology applications, which require good quality reusable models integral to the design, build, test and learn cycle.

resultsAs part of an ongoing effort to improve genome scale metabolic analysis, we have developed a test-driven development methodology for the continuous integration of validation data from different sources. Contributing to the open source technology based around COBRApy, we have developed the gsmodutils modelling framework placing an emphasis on test-driven design of models through defined test cases. Crucially, different conditions are configurable allowing users to examine how different designs or curation impact a wide range of system behaviours, minimizing error between model versions. AVAILABILITY AND IMPLEMENTATION: The software framework described within this paper is open source and freely available from http://github.com/SBRCNottingham/gsmodutils. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.

Indexed as

GenomeModels, BiologicalMetabolic EngineeringSoftwareSystems Biology

Identifiers

PMID30759197
PMCPMC6748746

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.