Evidence map›Paper›PMID 40203028›Full record

ArticlePloS one2025

Utilizing a deep learning model based on BERT for identifying enhancers and their strength.

Tong Wang, Mengqi Gao

Abstract read
In one paragraph

Article in PloS one, 2025. 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. Review
  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

2 authors.

Tong WangSchool of Computer and Information Engineering, Shanghai Polytechnic University, Shanghai, China.ORCID 0000-0001-8622-3560
Mengqi GaoSchool of Computer and Information Engineering, Shanghai Polytechnic University, Shanghai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An enhancer is a specific DNA sequence typically located within a gene at upstream or downstream position and serves as a pivotal element in the regulation of eukaryotic gene transcription. Therefore, the recognition of enhancers is highly significant for comprehending gene expression regulatory systems. While some useful predictive models have been proposed, there are still deficiencies in these models. To address current limitations, we propose a model, DNABERT2-Enhancer, based on transformer architecture and deep learning, designed for the recognition of enhancers (classified as either enhancer or non-enhancer) and the identification of their activity (strong or weak enhancers). More specifically, DNABERT2-Enhancer is composed of a BERT model for extracting features and a CNN model for enhancers classification. Parameters of the BERT model are initialized by a pre-training DNABERT-2 language model. The enhancer recognition task is then fine-tuned through transfer learning to convert the original sequence into feature vectors. Subsequently, the CNN network is employed to learn the feature vector generated by BERT and produce the prediction results. In comparison with existing predictors utilizing the identical dataset, our approach demonstrates superior performance. This suggests that the model will be a useful instrument for academic research on the enhancer recognition.

Indexed as

Deep LearningEnhancer Elements, GeneticAlgorithmsComputational BiologyHumansNeural Networks, Computer

Identifiers

PMID40203028
PMCPMC11981215

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.