Evidence map›Paper›PMID 40131313›Full record

ArticleBriefings in bioinformatics2025

deepTAD: an approach for identifying topologically associated domains based on convolutional neural network and transformer model.

Xiaoyan Wang, Junwei Luo, Lili Wu, Huimin Luo, Fei Guo

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Xiaoyan WangSchool of Software, Henan Polytechnic University, 2001 Century Road, Jiaozuo 454003, China.
Junwei LuoSchool of Software, Henan Polytechnic University, 2001 Century Road, Jiaozuo 454003, China.ORCID 0000-0001-6841-9893
Lili WuSchool of Software, Henan Polytechnic University, 2001 Century Road, Jiaozuo 454003, China.
Huimin LuoSchool of Computer and Information Engineering, Henan University, North Section of Jinming Avenue, Kaifeng 475001, China.ORCID 0000-0002-5066-5372
Fei GuoSchool of Computer Science and Engineering, Central South University, 932 Lushan South Road, Changsha 410083, China.

Funding

Henan Provincial Department of Science and Technology Research Project 232102211046National Natural Science Foundation of China 62372156
6 · The paper itself

Abstract

motivationTopologically associated domains (TADs) play a key role in the 3D organization and function of genomes, and accurate detection of TADs is essential for revealing the relationship between genomic structure and function. Most current methods are developed to extract features in Hi-C interaction matrix to identify TADs. However, due to complexities in Hi-C contact matrices, it is difficult to directly extract features associated with TADs, which prevents current methods from identifying accurate TADs.

resultsIn this paper, a novel method is proposed, deepTAD, which is developed based on a convolutional neural network (CNN) and transformer model. First, based on Hi-C contact matrix, deepTAD utilizes CNN to directly extract features associated with TAD boundaries. Next, deepTAD takes advantage of the transformer model to analyze the variation features around TAD boundaries and determines the TAD boundaries. Second, deepTAD uses the Wilcoxon rank-sum test to further identify false-positive boundaries. Finally, deepTAD computes cosine similarity among identified TAD boundaries and assembles TAD boundaries to obtain hierarchical TADs. The experimental results show that TAD boundaries identified by deepTAD have a significant enrichment of biological features, including structural proteins, histone modifications, and transcription start site loci. Additionally, when evaluating the completeness and accuracy of identified TADs, deepTAD has a good performance compared with other methods. The source code of deepTAD is available at https://github.com/xiaoyan-wang99/deepTAD.

Indexed as

ChromatinComputational BiologyGenomicsNeural Networks, ComputerSoftwareAlgorithmsConvolutional Neural NetworksHumansChromatinconvolutional neural networkthree-dimensional genometopologically associating domainstransformer

Identifiers

PMID40131313
PMCPMC11934553

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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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.