Evidence map›Paper›PMID 23985733›Full record

ArticleJournal of the Royal Society, Interface2013

Designing experiments to understand the variability in biochemical reaction networks.

Jakob Ruess, Andreas Milias-Argeitis, John Lygeros

Open access · bronzeAbstract read
In one paragraph

Article in Journal of the Royal Society, Interface, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

23 citing papers in PubMed, 78 citations in OpenAlex.

  1. Uncertainty Quantification forChemical reviews · 2026
    Review
  2. Sequential design of single-cell experiments to identify discrete stochastic models for gene expression.Proceedings of the ... IEEE Conference on Decision & Control. IEEE Conference on Decision & Control · 2024
    Article
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  14. Distribution shapes govern the discovery of predictive models for gene regulation.Proceedings of the National Academy of Sciences of the United States of America · 2018
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  17. Reconstructing dynamic molecular states from single-cell time series.Journal of the Royal Society, Interface · 2016
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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

3 authors at 2 institutions in 3 countries.

Jakob RuessAutomatic Control Laboratory, ETH Zurich, 8092 Zurich, Switzerland.
Andreas Milias-Argeitis
John Lygeros
Google (United States) · USAgios Andreas Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Exploiting the information provided by the molecular noise of a biological process has proved to be valuable in extracting knowledge about the underlying kinetic parameters and sources of variability from single-cell measurements. However, quantifying this additional information a priori, to decide whether a single-cell experiment might be beneficial, is currently only possible in systems where either the chemical master equation is computationally tractable or a Gaussian approximation is appropriate. Here, we provide formulae for computing the information provided by measured means and variances from the first four moments and the parameter derivatives of the first two moments of the underlying process. For stochastic kinetic models for which these moments can be either computed exactly or approximated efficiently, the derived formulae can be used to approximate the information provided by single-cell distribution experiments. Based on this result, we propose an optimal experimental design framework which we employ to compare the utility of dual-reporter and perturbation experiments for quantifying the different noise sources in a simple model of gene expression. Subsequently, we compare the information content of a set of experiments which have been performed in an engineered light-switch gene expression system in yeast and show that well-chosen gene induction patterns may allow one to identify features of the system which remain hidden in unplanned experiments.

Indexed as

Computer SimulationModels, BiologicalResearch DesignStochastic Processescell-to-cell variabilitycontinuous-time Markov chainsFisher informationgene expressionoptimal experimental design

Identifiers

PMID23985733
PMCPMC3785824
OpenAlexW2158912722

What OpenQuestion holds

Textmetadata
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.