Evidence map›Paper›PMID 24578401›Full record

ArticleBioinformatics (Oxford, England)2014

Derivative processes for modelling metabolic fluxes.

Justina Zurauskienė, Paul Kirk, Thomas Thorne, John Pinney, Michael Stumpf

Open access · hybridAbstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.1field-weighted citation impact, top 45% of its field
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

3 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Gaussian Process Modeling of Protein Turnover.Journal of proteome research · 2016
    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

5 authors at 1 institution in 1 country.

Justina ZurauskienėTheoretical Systems Biology Group, Centre for Bioinformatics, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Paul KirkTheoretical Systems Biology Group, Centre for Bioinformatics, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Thomas ThorneTheoretical Systems Biology Group, Centre for Bioinformatics, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
John PinneyTheoretical Systems Biology Group, Centre for Bioinformatics, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Michael StumpfTheoretical Systems Biology Group, Centre for Bioinformatics, Imperial College London, South Kensington Campus, London SW7 2AZ, UK.
Imperial College London · GB

Funding

Biotechnology and Biological Sciences Research Council BB/G020434/1
6 · The paper itself

Abstract

motivationOne of the challenging questions in modelling biological systems is to characterize the functional forms of the processes that control and orchestrate molecular and cellular phenotypes. Recently proposed methods for the analysis of metabolic pathways, for example, dynamic flux estimation, can only provide estimates of the underlying fluxes at discrete time points but fail to capture the complete temporal behaviour. To describe the dynamic variation of the fluxes, we additionally require the assumption of specific functional forms that can capture the temporal behaviour. However, it also remains unclear how to address the noise which might be present in experimentally measured metabolite concentrations.

resultsHere we propose a novel approach to modelling metabolic fluxes: derivative processes that are based on multiple-output Gaussian processes (MGPs), which are a flexible non-parametric Bayesian modelling technique. The main advantages that follow from MGPs approach include the natural non-parametric representation of the fluxes and ability to impute the missing data in between the measurements. Our derivative process approach allows us to model changes in metabolite derivative concentrations and to characterize the temporal behaviour of metabolic fluxes from time course data. Because the derivative of a Gaussian process is itself a Gaussian process, we can readily link metabolite concentrations to metabolic fluxes and vice versa. Here we discuss how this can be implemented in an MGP framework and illustrate its application to simple models, including nitrogen metabolism in Escherichia coli. AVAILABILITY AND IMPLEMENTATION: R code is available from the authors upon request.

Indexed as

Metabolic Networks and PathwaysBayes TheoremEscherichia coliModels, BiologicalNitrogenNitrogen

Identifiers

PMID24578401
PMCPMC4071196
OpenAlexW2102892614

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.