Evidence map›Paper›PMID 41721174›Full record

ArticleBulletin of mathematical biology2026

Inference of Genetic Networks from Pseudo Time Series of Single-cell Gene Expression Data using Modified Random Forests.

Shuhei Kimura, Ryosuke Misaki, Masato Tokuhisa, Keita Iida, Mariko Okada

Abstract read
In one paragraph

Article in Bulletin of mathematical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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

5 authors.

Shuhei KimuraFaculty of Engineering, Tottori University, 4-101, Koyama-minami, Tottori, 680-8552, Japan. kimura@tottori-u.ac.jp.ORCID http://orcid.org/0000-0002-6246-2636
Ryosuke MisakiGraduate School of Sustainability Sciences, Tottori University, 4-101, Koyama-minami, Tottori, 680-8552, Japan.
Masato TokuhisaFaculty of Engineering, Tottori University, 4-101, Koyama-minami, Tottori, 680-8552, Japan.
Keita IidaInstitute for Protein Research, Osaka University, 3-2, Yamadaoka, Suita, 565-0871, Japan.
Mariko OkadaInstitute for Protein Research, Osaka University, 3-2, Yamadaoka, Suita, 565-0871, Japan.

Funding

KAKENHI 22K12193
6 · The paper itself

Abstract

This study proposes a novel method for inferring genetic networks using both steady-state and pseudo time-series data of single-cell gene expressions. While several methods for inferring genetic networks from time series of bulk-cell gene expression data have been proposed, many of these approaches use time derivatives of gene expression levels. However, since pseudo time-series data lack precise temporal information about when measurements were taken, time derivatives cannot be calculated from this data. Therefore, existing methods are ineffective for analyzing pseudo time-series data. To address this limitation, our proposed method does not use time derivatives of gene expression levels but uses their signs. We theorize that, even when no precise temporal information is available, the signs of time derivatives, which indicate whether the gene expression levels are increasing or decreasing, can be estimated from pseudo time-series data. Our approach was designed on the basis of GENIE3 and its extensions, which, although essentially intended to infer genetic networks from bulk-cell gene expression data, have reportedly performed well in this respect. Validation through numerical experiments with both artificial and real gene expression data confirms the effectiveness of our proposed method.

Indexed as

Gene Regulatory NetworksModels, GeneticAlgorithmsComputational BiologyComputer SimulationGene Expression ProfilingMathematical ConceptsRandom ForestSingle-Cell AnalysisSingle-Cell Gene Expression AnalysisGenetic networkGENIE3Pseudo time-series datascRNA-seq

Identifiers

PMID41721174
PMCPMC12923446

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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.