Evidence map›Paper›PMID 42681526›Full record

ReviewMethods in molecular biology (Clifton, N.J.)2026

Drug Discovery from Gene Expression/Gene Regulation.

Yi Cong, Toshinori Endo

Abstract readReview
PubMed Publisher
In one paragraph

Review in Methods in molecular biology (Clifton, N.J.), 2026. 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
–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

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

2 authors.

Yi CongInformation Biology Laboratory, Graduate School of Information Science and Technology, Hokkaido University, N14W9, Sapporo, 060-0814, Japan.ORCID 0009-0007-9281-9951
Toshinori EndoInformation Biology Laboratory, Faculty of Information Science and Technology, Hokkaido University, N14W9, Sapporo, 060-0814, Japan. endo@ist.hokudai.ac.jp.ORCID 0000-0002-5711-2527

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene expression and gene regulation play critical roles in understanding disease mechanisms, identifying therapeutic targets, and guiding drug discovery. Advances in high-throughput sequencing technologies, such as next-generation sequencing (NGS) and single-cell RNA sequencing (scRNA-seq), have enabled comprehensive profiling of gene expression across diverse biological contexts. Computational methods, including machine learning (ML) and deep learning (DL), have further revolutionized transcriptomic and regulatory analyses by uncovering complex gene interactions and predicting disease-associated regulatory networks. This chapter explores the integration of AI-driven approaches in gene expression analysis, focusing on differential expression analysis, clustering techniques, and gene regulatory network (GRN) inference. We discuss the role of dimensionality reduction and unsupervised learning in identifying disease subtypes and patient stratification, as well as how single-cell transcriptomics enhances our understanding of cellular heterogeneity in drug response and resistance. Furthermore, we examine network-based methodologies, highlighting the application of AI and ML in reconstructing GRNs, prioritizing regulatory targets, and facilitating drug repositioning. The emerging field of AI-assisted drug repositioning is also covered, with an emphasis on leveraging transcriptomic signatures and network-based inference to repurpose existing drugs for novel therapeutic applications. By integrating multiomics data and employing explainable AI frameworks, researchers can refine precision medicine strategies and accelerate the drug discovery process. Finally, we address current challenges in AI-driven gene analysis, including data complexity, model interpretability, and the integration of multiomics datasets. Future directions include advances in large language models (LLMs), spatial transcriptomics, and quantum-enhanced AI for predictive modeling. The convergence of AI, high-throughput sequencing, and network-based approaches promises to reshape biomedical research and optimize drug discovery pipelines for improved clinical outcomes.

Indexed as

Computational BiologyDrug DiscoveryGene Expression RegulationGene Regulatory NetworksDrug RepositioningGene Expression ProfilingHigh-Throughput Nucleotide SequencingHumansMachine LearningSingle-Cell Gene Expression AnalysisTranscriptomeAIDrug repositioningGene expressionGene regulationGRNsMachine learningMultiomicsNGSPrecision medicinescRNA-seq

Identifiers

PMID42681526

What OpenQuestion holds

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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.