Evidence map›Paper›PMID 26389116›Full record

ArticleFrontiers in bioengineering and biotechnology2015

Designing Experiments to Discriminate Families of Logic Models.

Santiago Videla, Irina Konokotina, Leonidas G Alexopoulos, Julio Saez-Rodriguez, Torsten Schaub, Anne Siegel, Carito Guziolowski

Abstract read
In one paragraph

Article in Frontiers in bioengineering and biotechnology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
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  5. Review
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  7. A Six-Stage Workflow for Robust Application of Systems Pharmacology.CPT: pharmacometrics & systems pharmacology · 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

7 authors.

Santiago VidelaUMR 6074 IRISA, CNRS, Campus de Beaulieu , Rennes , France ; Dyliss project, INRIA, Campus de Beaulieu , Rennes , France ; Institut für Informatik, Universität Potsdam , Potsdam , Germany ; LBSI, Fundación Instituto Leloir, CONICET , Buenos Aires , Argentina.
Irina KonokotinaIRCCyN UMR CNRS 6597, École Centrale de Nantes , Nantes , France.
Leonidas G AlexopoulosDepartment of Mechanical Engineering, National Technical University of Athens , Athens , Greece.
Julio Saez-RodriguezEuropean Molecular Biology Laboratory, European Bioinformatics Institute , Hinxton , UK.
Torsten SchaubInstitut für Informatik, Universität Potsdam , Potsdam , Germany.
Anne SiegelUMR 6074 IRISA, CNRS, Campus de Beaulieu , Rennes , France ; Dyliss project, INRIA, Campus de Beaulieu , Rennes , France.
Carito GuziolowskiIRCCyN UMR CNRS 6597, École Centrale de Nantes , Nantes , France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Logic models of signaling pathways are a promising way of building effective in silico functional models of a cell, in particular of signaling pathways. The automated learning of Boolean logic models describing signaling pathways can be achieved by training to phosphoproteomics data, which is particularly useful if it is measured upon different combinations of perturbations in a high-throughput fashion. However, in practice, the number and type of allowed perturbations are not exhaustive. Moreover, experimental data are unavoidably subjected to noise. As a result, the learning process results in a family of feasible logical networks rather than in a single model. This family is composed of logic models implementing different internal wirings for the system and therefore the predictions of experiments from this family may present a significant level of variability, and hence uncertainty. In this paper, we introduce a method based on Answer Set Programming to propose an optimal experimental design that aims to narrow down the variability (in terms of input-output behaviors) within families of logical models learned from experimental data. We study how the fitness with respect to the data can be improved after an optimal selection of signaling perturbations and how we learn optimal logic models with minimal number of experiments. The methods are applied on signaling pathways in human liver cells and phosphoproteomics experimental data. Using 25% of the experiments, we obtained logical models with fitness scores (mean square error) 15% close to the ones obtained using all experiments, illustrating the impact that our approach can have on the design of experiments for efficient model calibration.

Indexed as

answer set programmingBoolean logic modelsexperimental designphosphoproteomicsignaling networks

Identifiers

PMID26389116
PMCPMC4560026

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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.