Evidence map›Paper›PMID 41634097›Full record

ArticleScientific reports2026

A DNABERT based deep learning framework for predicting transcription factor binding sites.

Pratik Dutta, Nimisha Ghosh, Daniele Santoni

Abstract read
In one paragraph

Article in Scientific reports, 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
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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

The trial behind it

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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

3 authors.

Pratik Dutta *Department of Computer Science and Engineering, Siksha 'O' Anusandhan (Deemed to be University), Bhubaneswar, India. pratikdutta@soa.ac.in.
Nimisha Ghosh *Department of Computer Science and Engineering, Shiv Nadar University Chennai, Chennai, Tamil Nadu, India.
Daniele SantoniInstitute for System Analysis and Computer Science "Antonio Ruberti", National Research Council of Italy, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Transcription factors are proteins that regulate the expression of genes by binding to specific genomic regions known as Transcription Factor Binding Sites (TFBSs), typically located in the promoter regions of those genes. Accurate prediction of these binding sites is essential for understanding the complex gene regulatory networks underlying various cellular functions. In this regard, many deep learning models have been developed for such prediction, but there is still scope of improvement. In this work, we have developed a deep learning model which uses pre-trained DNABERT, a convolutional neural network (CNN) module, a modified convolutional block attention module (MCBAM), a multi-scale convolutions with attention (MSCA) module and an output module. The pre-trained DNABERT is used for sequence embedding, thereby capturing the long-term dependencies in the DNA sequences while the CNN, MCBAM and MSCA modules are useful in extracting higher-order local features. The proposed model TFBS-Finder is trained and tested on 165 ENCODE ChIP-seq datasets. We have also performed ablation studies as well as cross-cell line validations and comparisons with other models. The experimental results show the superiority of the proposed method in predicting TFBSs compared to the existing methodologies. Furthermore, we have performed visual analysis to show the interpretability of the prediction results. The source code of the proposed model is available at https://github.com/NimishaGhosh/TFBS-Finder.

Indexed as

Computational BiologyDeep LearningTranscription FactorsBinding SitesConvolutional Neural NetworksHumansPromoter Regions, GeneticProtein BindingTranscription FactorsDeep LearningDNABERTDNA SequencesTranscription Factor Binding Sites

Identifiers

PMID41634097
PMCPMC12921214

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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 Socratic graph.