A novel deep learning framework with dynamic tokenization for identifying chromatin interactions along with motif importance investigation

A comprehensive understanding of chromatin interaction networks is crucial for unraveling the regulatory mechanisms of gene expression. While various computational methods have been developed to predict chromatin interactions and address the limitations and high costs of high-throughput experimental techniques, their performance is often overestimated due to the specificity of chromatin interaction data. In this study, we proposed Inter-Chrom, a novel deep learning model integrating dynamic tokenization, DNABERT's word embedding, and the efficient channel attention mechanism to identify chromatin interactions using sequence and genomic features, leveraging a newly curated dataset. Experimental results demonstrate that Inter-Chrom outperforms existing methods on three cell line datasets. Additionally, we proposed a novel method for calculating motif importance and analyzed the motifs with high importance scores identified through this method, including those that have been extensively studied and others that have received limited attention to date. Inter-Chrom's robustness for input variations and superior ability to leverage sequence features position it as a powerful tool for advancing chromatin interaction research. The source code of Inter-Chrom is freely available at https://github.com/HaoWuLab-Bioinformatics/Inter-Chrom.

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Publication Details

Journal
Briefings in Bioinformatics
Published
2025-05-01
DOI
https://doi.org/10.1093/bib/bbaf289
Citations
15
Primary Topic
Genomics and Chromatin Dynamics
Type
article
Field-Weighted Citation Impact
12.09

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article

A novel deep learning framework with dynamic tokenization for identifying chromatin interactions along with motif importance investigation

Hao Wu, Xin Li, Liangcan Li
15 citations
Briefings in Bioinformatics
Genomics and Chromatin Dynamics
12.09
article

A novel deep learning framework with dynamic tokenization for identifying chromatin interactions along with motif importance investigation

Hao Wu, Xin Li, Liangcan Li
article en
15 citations

Abstract

A comprehensive understanding of chromatin interaction networks is crucial for unraveling the regulatory mechanisms of gene expression. While various computational methods have been developed to predict chromatin interactions and address the limitations and high costs of high-throughput experimental techniques, their performance is often overestimated due to the specificity of chromatin interaction data. In this study, we proposed Inter-Chrom, a novel deep learning model integrating dynamic tokenization, DNABERT's word embedding, and the efficient channel attention mechanism to identify chromatin interactions using sequence and genomic features, leveraging a newly curated dataset. Experimental results demonstrate that Inter-Chrom outperforms existing methods on three cell line datasets. Additionally, we proposed a novel method for calculating motif importance and analyzed the motifs with high importance scores identified through this method, including those that have been extensively studied and others that have received limited attention to date. Inter-Chrom's robustness for input variations and superior ability to leverage sequence features position it as a powerful tool for advancing chromatin interaction research. The source code of Inter-Chrom is freely available at https://github.com/HaoWuLab-Bioinformatics/Inter-Chrom.

Briefings in BioinformaticsVol. 26(3)
Shandong University (CN), City University of Hong Kong, Shenzhen Research Institute (CN)
National Natural Science Foundation of China, National Key Research and Development Program of China, Basic and Applied Basic Research Foundation of Guangdong Province
Partnerships for the goals
Openalex Percentile: Top 1%
Genomics and Chromatin Dynamics
12.09
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A novel deep learning framework with dynamic tokenization for identifying chromatin interactions along with motif importance investigation — Hao Wu, Xin Li, et al. · Briefings in Bioinformatics (2025) | TGRS Research Map | TGRS