Evidence map›Paper›PMID 29928721›Full record

ArticleInfectious Disease Modelling2016

Controllability and stability analysis of large transcriptomic dynamic systems for host response to influenza infection in human.

Xiaodian Sun, Fang Hu, Shuang Wu, Xing Qiu, Patrice Linel, Hulin Wu

Abstract read
In one paragraph

Article in Infectious Disease Modelling, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Modelling of hypoxia gene expression for three different cancer cell lines.International journal of computational biology and drug design · 2020
    Article
  3. Order Through Disorder: The Characteristic Variability of Systems.Frontiers in cell and developmental biology · 2020
    Review
  4. Article
  5. Restructured GEO: restructuring Gene Expression Omnibus metadata for genome dynamics analysis.Database : the journal of biological databases and curation · 2019
    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

6 authors.

Xiaodian SunBiostatistics and Bioinformatics Core, Sylvester Comprehensive Cancer Center, University of Miami, Miami, USA.
Fang HuDepartment of Biostatistics and Computational Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Shuang WuGenus PLC, ABS Global, Deforest, WI, USA.
Xing QiuDepartment of Biostatistics and Computational Biology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA.
Patrice LinelGenus PLC, ABS Global, Deforest, WI, USA.
Hulin WuDepartment of Biostatistics, School of Public Health, University of Texas Health Science Center at Houston, Houston, TX, USA.

Funding

Virology/Immunology CoreP30AI078498 · NIAID · UNIVERSITY OF ROCHESTER · PI DEWHURST, STEPHEN · 2008 to 2018
$14.6M
Statistical Methods for ODE Models in AIDS ResearchR01AI087135 · NIAID · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI WU, HULIN · 2010 to 2019
$3.2M
NIAID NIH HHS HHSN266200700008CNIAID NIH HHS HHSN272201000055CNIAID NIH HHS P30 AI078498NIAID NIH HHS R01 AI087135
6 · The paper itself

Abstract

backgroundGene regulatory networks are complex dynamic systems and the reverse-engineering of such networks from high-dimensional time course transcriptomic data have attracted researchers from various fields. It is also interesting and important to study the behavior of the reconstructed networks on the basis of dynamic models and the biological mechanisms. We focus on the gene regulatory networks reconstructed using the ordinary differential equation (ODE) modelling approach and investigate the properties of these networks.

resultsControllability and stability analyses are conducted for the reconstructed gene response networks of 17 influenza infected subjects based on ODE models. Symptomatic subjects tend to have larger numbers of driver nodes, higher proportions of critical links and lower proportions of redundant links than asymptomatic subjects. We also show that the degree distribution, rather than the structure of networks, plays an important role in controlling the network in response to influenza infection. In addition, we find that the stability of high-dimensional networks is very sensitive to randomness in the reconstructed systems brought by errors in measurements and parameter estimation.

conclusionsThe gene response networks of asymptomatic subjects are easier to be controlled than those of symptomatic subjects. This may indicate that the regulatory systems of asymptomatic subjects are easier to recover from disease stimulations, so these subjects are less likely to develop symptoms. Our results also suggest that stability constraint should be considered in the modelling of high-dimensional networks and the estimation of network parameters.

Identifiers

PMID29928721
PMCPMC5963324

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Registered trials

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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.