Evidence map›Paper›PMID 39679439›Full record

ArticleBriefings in bioinformatics2024

A self-attention-driven deep learning framework for inference of transcriptional gene regulatory networks.

Yong Liu, Le Zhong, Bin Yan, Zhuobin Chen, Yanjia Yu, Dan Yu, Jing Qin, Junwen Wang

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

8 authors.

Yong LiuCollege of Electronic Information, Guangxi Minzu University, 188 East University Road, Nanning, Guangxi, 530006, China.
Le ZhongCollege of Electronic Information, Guangxi Minzu University, 188 East University Road, Nanning, Guangxi, 530006, China.
Bin YanDivision of Applied Oral Sciences & Community Dental Care, Faculty of Dentistry, The University of Hong Kong, 34 Hospital Road, Hong Kong SAR, China.
Zhuobin ChenSchool of Pharmaceutical Sciences (Shenzhen), Shenzhen Campus of Sun Yat-sen University, 66 Gongchang Road, Shenzhen, Guangdong, 518107, China.
Yanjia YuCollege of Electronic Information, Guangxi Minzu University, 188 East University Road, Nanning, Guangxi, 530006, China.
Dan YuDivision of Applied Oral Sciences & Community Dental Care, Faculty of Dentistry, The University of Hong Kong, 34 Hospital Road, Hong Kong SAR, China.
Jing QinSchool of Pharmaceutical Sciences (Shenzhen), Shenzhen Campus of Sun Yat-sen University, 66 Gongchang Road, Shenzhen, Guangdong, 518107, China.ORCID 0000-0002-8327-8846
Junwen WangDivision of Applied Oral Sciences & Community Dental Care, Faculty of Dentistry, The University of Hong Kong, 34 Hospital Road, Hong Kong SAR, China.ORCID 0000-0002-4432-4707

Funding

Discover and Analyze Germline-Somatic Interactions in CancerR01LM013438 · NLM · ARIZONA STATE UNIVERSITY-TEMPE CAMPUS · PI LIU, LI, YANG, PING · 2021 to 2023
$1.0M
Faculty of Dentistry, the University of Hong KongHong Kong Research Grants Council C7015-23GNational Institutes of Health of USA R01LM013438National Natural Science Foundation of China 32170655Natural Science Foundation of Guangdong Province 2024A1515011210NLM NIH HHS R01 LM013438Shenzhen Science and Technology Program 202206193000001University of Hong Kong 207051059
6 · The paper itself

Abstract

The interactions between transcription factors (TFs) and the target genes could provide a basis for constructing gene regulatory networks (GRNs) for mechanistic understanding of various biological complex processes. From gene expression data, particularly single-cell transcriptomic data containing rich cell-to-cell variations, it is highly desirable to infer TF-gene interactions (TGIs) using deep learning technologies. Numerous models or software including deep learning-based algorithms have been designed to identify transcriptional regulatory relationships between TFs and the downstream genes. However, these methods do not significantly improve predictions of TGIs due to some limitations regarding constructing underlying interactive structures linking regulatory components. In this study, we introduce a deep learning framework, DeepTGI, that encodes gene expression profiles from single-cell and/or bulk transcriptomic data and predicts TGIs with high accuracy. Our approach could fuse the features extracted from Auto-encoder with self-attention mechanism and other networks and could transform multihead attention modules to define representative features. By comparing it with other models or methods, DeepTGI exhibits its superiority to identify more potential TGIs and to reconstruct the GRNs and, therefore, could provide broader perspectives for discovery of more biological meaningful TGIs and for understanding transcriptional gene regulatory mechanisms.

Indexed as

Deep LearningGene Regulatory NetworksTranscription FactorsAlgorithmsComputational BiologyGene Expression ProfilingGene Expression RegulationHumansSoftwareTranscriptomeTranscription Factorsdeep learninggene regulatory networksself-attention mechanismsingle-cell transcriptomic datatranscription factor-gene interaction

Identifiers

PMID39679439
PMCPMC11647272

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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.