Evidence map›Paper›PMID 38062373›Full record

ArticleBMC bioinformatics2023

Efficient design of synthetic gene circuits under cell-to-cell variability.

Baptiste Turpin, Eline Y Bijman, Hans-Michael Kaltenbach, Jörg Stelling

Abstract read
In one paragraph

Article in BMC bioinformatics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

4 authors.

Baptiste TurpinDepartment of Biosystems Science and Engineering (D-BSSE) and SIB Swiss Institute of Bioinformatics, ETH Zurich, 4058, Basel, Switzerland.
Eline Y BijmanDepartment of Biosystems Science and Engineering (D-BSSE) and SIB Swiss Institute of Bioinformatics, ETH Zurich, 4058, Basel, Switzerland.
Hans-Michael KaltenbachDepartment of Biosystems Science and Engineering (D-BSSE) and SIB Swiss Institute of Bioinformatics, ETH Zurich, 4058, Basel, Switzerland.ORCID http://orcid.org/0000-0003-2500-1221
Jörg StellingDepartment of Biosystems Science and Engineering (D-BSSE) and SIB Swiss Institute of Bioinformatics, ETH Zurich, 4058, Basel, Switzerland. joerg.stelling@bsse.ethz.ch.ORCID http://orcid.org/0000-0002-1145-891X

Funding

Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung 182895
6 · The paper itself

Abstract

backgroundSynthetic biologists use and combine diverse biological parts to build systems such as genetic circuits that perform desirable functions in, for example, biomedical or industrial applications. Computer-aided design methods have been developed to help choose appropriate network structures and biological parts for a given design objective. However, they almost always model the behavior of the network in an average cell, despite pervasive cell-to-cell variability.

resultsHere, we present a computational framework and an efficient algorithm to guide the design of synthetic biological circuits while accounting for cell-to-cell variability explicitly. Our design method integrates a Non-linear Mixed-Effects (NLME) framework into a Markov Chain Monte-Carlo (MCMC) algorithm for design based on ordinary differential equation (ODE) models. The analysis of a recently developed transcriptional controller demonstrates first insights into design guidelines when trying to achieve reliable performance under cell-to-cell variability.

conclusionWe anticipate that our method not only facilitates the rational design of synthetic networks under cell-to-cell variability, but also enables novel applications by supporting design objectives that specify the desired behavior of cell populations.

Indexed as

Gene Regulatory NetworksGenes, SyntheticAlgorithmsComputer-Aided DesignMarkov ChainsSynthetic BiologyCell-to-cell variabilityComputer-aided designSynthetic biology

Identifiers

PMID38062373
PMCPMC10701960

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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.