Evidence map›Paper›PMID 35030172›Full record

ArticlePLoS computational biology2022

Identification of periodic attractors in Boolean networks using a priori information.

Ulrike Münzner, Tomoya Mori, Marcus Krantz, Edda Klipp, Tatsuya Akutsu

Open access · goldAbstract read
In one paragraph

Article in PLoS computational biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 60% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. Attractor detection and enumeration algorithms for Boolean networks.Computational and structural biotechnology journal · 2022
    Review
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

5 authors at 2 institutions in 2 countries.

Ulrike MünznerInstitute for Protein Research, Laboratory of Cell Systems, Osaka University, Suita, Osaka, Japan.ORCID 0000-0002-8939-7643
Tomoya MoriInstitute for Chemical Research, Bioinformatics Center, Kyoto University, Kyoto, Japan.ORCID 0000-0003-3483-0056
Marcus KrantzInstitute of Biology, Theoretical Biophysics, Humboldt-Universität zu Berlin, Berlin, Germany.ORCID 0000-0001-7843-8342
Edda KlippInstitute of Biology, Theoretical Biophysics, Humboldt-Universität zu Berlin, Berlin, Germany.ORCID 0000-0002-0567-7075
Tatsuya AkutsuInstitute for Chemical Research, Bioinformatics Center, Kyoto University, Kyoto, Japan.ORCID 0000-0001-9763-797X
Kyoto University · JPHumboldt-Universität zu Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Boolean networks (BNs) have been developed to describe various biological processes, which requires analysis of attractors, the long-term stable states. While many methods have been proposed to detection and enumeration of attractors, there are no methods which have been demonstrated to be theoretically better than the naive method and be practically used for large biological BNs. Here, we present a novel method to calculate attractors based on a priori information, which works much and verifiably faster than the naive method. We apply the method to two BNs which differ in size, modeling formalism, and biological scope. Despite these differences, the method presented here provides a powerful tool for the analysis of both networks. First, our analysis of a BN studying the effect of the microenvironment during angiogenesis shows that the previously defined microenvironments inducing the specialized phalanx behavior in endothelial cells (ECs) additionally induce stalk behavior. We obtain this result from an extended network version which was previously not analyzed. Second, we were able to heuristically detect attractors in a cell cycle control network formalized as a bipartite Boolean model (bBM) with 3158 nodes. These attractors are directly interpretable in terms of genotype-to-phenotype relationships, allowing network validation equivalent to an in silico mutagenesis screen. Our approach contributes to the development of scalable analysis methods required for whole-cell modeling efforts.

Indexed as

AlgorithmsModels, BiologicalComputational BiologyComputer SimulationDatabases, GeneticEndothelial CellsMutagenesis

Identifiers

PMID35030172
PMCPMC8803189
OpenAlexW4205942940

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.