Evidence map›Paper›PMID 41697918›Full record

ArticleBriefings in bioinformatics2026

EPINTLM: enhancer-promoter prediction with pretrained k-mer embeddings and residual cross-attention.

Thi Lan Nguyen, Hien Quang Kha, Phat Ky Nguyen, Minh Huu Nhat Le, Duc-Trong Le, Nguyen Quoc Khanh Le

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 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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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Thi Lan NguyenVNU University of Engineering and Technology, Vietnam National University, 144 Xuan Thuy, Cau Giay, Hanoi 100000, Vietnam.
Hien Quang KhaAIBioMed Research Group, Taipei Medical University, 250 Wuxing Street, Taipei 110, Taiwan.
Phat Ky NguyenAIBioMed Research Group, Taipei Medical University, 250 Wuxing Street, Taipei 110, Taiwan.
Minh Huu Nhat LeAIBioMed Research Group, Taipei Medical University, 250 Wuxing Street, Taipei 110, Taiwan.
Duc-Trong LeVNU University of Engineering and Technology, Vietnam National University, 144 Xuan Thuy, Cau Giay, Hanoi 100000, Vietnam.
Nguyen Quoc Khanh LeAIBioMed Research Group, Taipei Medical University, 250 Wuxing Street, Taipei 110, Taiwan.ORCID 0000-0003-4896-7926

Funding

National Science and Technology Council, Taiwan NSTC114-2221-E-038-015
6 · The paper itself

Abstract

Enhancer-promoter interactions (EPIs) play an important role in gene regulation, yet experimental mapping remains costly and limited in coverage. As a result, computational approaches are commonly evaluated under curated benchmark datasets, which pose challenges related to long-range sequence modeling, multimodal feature integration, and reproducible preprocessing. In this study, we present EPINTLM (Enhancer-Promoter Interaction Nucleotide Transformer Large Model), a deep learning framework designed to investigate architectural strategies for EPI prediction under standardized benchmark settings. EPINTLM integrates DNA sequence representations and genomic features by leveraging pretrained k-mer embeddings from the Nucleotide Transformer and explicitly modeling intra- and inter-sequence dependencies through residual self-attention and bidirectional cross-attention. We additionally introduce a unified preprocessing pipeline to improve training efficiency and reproducibility, and perform post hoc motif analysis to provide limited interpretability of learned sequence patterns. Evaluated on a widely used benchmark across six human cell lines, EPINTLM achieves competitive area under the receiver operating characteristic curve (AUROC) and area under the precision-recall curve (AUPR) performance relative to existing methods, with ablation studies highlighting the contributions of cross-attention and residual aggregation. These results demonstrate the utility of explicit cross-attention designs for paired regulatory sequence modeling within current benchmark constraints.

Indexed as

Computational BiologyDeep LearningEnhancer Elements, GeneticPromoter Regions, GeneticHumanscross-attention mechanismenhancer–promoter interactiongenomic sequencemultimodal featurepretrained large language modelsresidual connection

Identifiers

PMID41697918
PMCPMC12908682

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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.