Evidence map›Paper›PMID 31548864›Full record

ArticleJournal of biological engineering2019

Computational analysis of viable parameter regions in models of synthetic biological systems.

Žiga Pušnik, Miha Mraz, Nikolaj Zimic, Miha Moškon

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Article in Journal of biological engineering, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 7 papers.

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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

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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

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3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Žiga PušnikUniversity of Ljubljana, Faculty of Computer and Information Science, Večna pot 113, Ljubljana, 1000 Slovenia.
Miha MrazUniversity of Ljubljana, Faculty of Computer and Information Science, Večna pot 113, Ljubljana, 1000 Slovenia.
Nikolaj ZimicUniversity of Ljubljana, Faculty of Computer and Information Science, Večna pot 113, Ljubljana, 1000 Slovenia.
Miha MoškonUniversity of Ljubljana, Faculty of Computer and Information Science, Večna pot 113, Ljubljana, 1000 Slovenia.ORCID 0000-0003-4600-1730

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGene regulatory networks with different topological and/or dynamical properties might exhibit similar behavior. System that is less perceptive for the perturbations of its internal and external factors should be preferred. Methods for sensitivity and robustness assessment have already been developed and can be roughly divided into local and global approaches. Local methods focus only on the local area around nominal parameter values. This can be problematic when parameters exhibits the desired behavior over a large range of parameter perturbations or when parameter values are unknown. Global methods, on the other hand, investigate the whole space of parameter values and mostly rely on different sampling techniques. This can be computationally inefficient. To address these shortcomings 'glocal' approaches were developed that apply global and local approaches in an effective and rigorous manner.

resultsHerein, we present a computational approach for 'glocal' analysis of viable parameter regions in biological models. The methodology is based on the exploration of high-dimensional viable parameter spaces with global and local sampling, clustering and dimensionality reduction techniques. The proposed methodology allows us to efficiently investigate the viable parameter space regions, evaluate the regions which exhibit the largest robustness, and to gather new insights regarding the size and connectivity of the viable parameter regions. We evaluate the proposed methodology on three different synthetic gene regulatory network models, i.e. the repressilator model, the model of the AC-DC circuit and the model of the edge-triggered master-slave D flip-flop.

conclusionsThe proposed methodology provides a rigorous assessment of the shape and size of viable parameter regions based on (1) the mathematical description of the biological system of interest, (2) constraints that define feasible parameter regions and (3) cost function that defines the desired or observed behavior of the system. These insights can be used to assess the robustness of biological systems, even in the case when parameter values are unknown and more importantly, even when there are multiple poorly connected viable parameter regions in the solution space. Moreover, the methodology can be efficiently applied to the analysis of biological systems that exhibit multiple modes of the targeted behavior.

Indexed as

AC-DC circuitBiological D flip-flopBiological modelComputational analysisGenetic algorithmsPrincipal componentsRepressilatorRobustnessViable parameter regions

Identifiers

PMID31548864
PMCPMC6751877

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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.