Evidence map›Paper›PMID 24376454›Full record

ArticleFrontiers in genetics2013

On the underlying assumptions of threshold Boolean networks as a model for genetic regulatory network behavior.

Van Tran, Matthew N McCall, Helene R McMurray, Anthony Almudevar

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 38% 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

3 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Boolean modelling as a logic-based dynamic approach in systems medicine.Computational and structural biotechnology journal · 2022
    Review
  3. 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

4 authors at 1 institution in 1 country.

Van TranDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center Rochester, NY, USA.
Matthew N McCallDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center Rochester, NY, USA.
Helene R McMurrayDepartment of Biomedical Genetics, University of Rochester Medical Center Rochester, NY, USA.
Anthony AlmudevarDepartment of Biostatistics and Computational Biology, University of Rochester Medical Center Rochester, NY, USA.
University of Rochester Medical Center · US

Funding

TRAINING IN ENVIRONMENTAL HEALTH SCIENCES BIOSTATISTICST32ES007271 · NIEHS · UNIVERSITY OF ROCHESTER · PI Sally W Thurston · 1992 to 2026
$3.9M
CANCER RESEARCH TRAINING-EXPERIMENTAL THERAPY MODELST32CA009363 · NCI · UNIVERSITY OF ROCHESTER · PI LAND, HARTMUT · 1985 to 2013
$2.9M
Statistical Methods for Estimation of Gene Regulatory NetworksR00HG006853 · NHGRI · UNIVERSITY OF ROCHESTER · PI MCCALL, MATTHEW NICHOLSON · 2014 to 2016
$726k
Statistical Methods for Estimation of Gene Regulatory NetworksK99HG006853 · NHGRI · UNIVERSITY OF ROCHESTER · PI MCCALL, MATTHEW NICHOLSON · 2013 to 2013
$80k
NCI NIH HHS T32 CA009363NHGRI NIH HHS K99 HG006853NHGRI NIH HHS R00 HG006853NIEHS NIH HHS T32 ES007271
6 · The paper itself

Abstract

Boolean networks (BoN) are relatively simple and interpretable models of gene regulatory networks. Specifying these models with fewer parameters while retaining their ability to describe complex regulatory relationships is an ongoing methodological challenge. Additionally, extending these models to incorporate variable gene decay rates, asynchronous gene response, and synergistic regulation while maintaining their Markovian nature increases the applicability of these models to genetic regulatory networks (GRN). We explore a previously-proposed class of BoNs characterized by linear threshold functions, which we refer to as threshold Boolean networks (TBN). Compared to traditional BoNs with unconstrained transition functions, these models require far fewer parameters and offer a more direct interpretation. However, the functional form of a TBN does result in a reduction in the regulatory relationships which can be modeled. We show that TBNs can be readily extended to permit self-degradation, with explicitly modeled degradation rates. We note that the introduction of variable degradation compromises the Markovian property fundamental to BoN models but show that a simple state augmentation procedure restores their Markovian nature. Next, we study the effect of assumptions regarding self-degradation on the set of possible steady states. Our findings are captured in two theorems relating self-degradation and regulatory feedback to the steady state behavior of a TBN. Finally, we explore assumptions of synchronous gene response and asynergistic regulation and show that TBNs can be easily extended to relax these assumptions. Applying our methods to the budding yeast cell-cycle network revealed that although the network is complex, its steady state is simplified by the presence of self-degradation and lack of purely positive regulatory cycles.

Indexed as

asynchronous updateattractorBoolean networkfeedback loopgenetic regulatory networkstate augmentationsteady stateyeast cell-cycle

Identifiers

PMID24376454
PMCPMC3859184
OpenAlexW2037431368

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.