Neural Network-Based Ensemble Learning Model to Identify Antigenic Fragments of SARS-CoV-2

The development of epitope-based vaccines (EBVs) necessitates the identification of antigenic fragments (AFs) of the target pathogen known as T-cell epitopes (TCEs). TCEs are recognized by immune system, specifically by T cells, B cells, and antibodies. Traditional wet lab methods for identifying TCEs are often costly, challenging, and time-consuming compared to computational approaches. In this study, we propose a neural network-based ensemble machine learning (ML) model trained on physicochemical properties of SARS-CoV-2 peptides sequences to predict TCE sequences. The performance of the model assessed using test dataset demonstrated an accuracy of >95%, surpassing the results of other ML classifiers that were employed for comparative analysis. Through fivefold cross-validation technique, a mean accuracy of approximately 95% was reported. Additionally, when compared to other existing TCE prediction methods using a blind dataset, the proposed model was found to be more accurate and effective. The predicted epitopes may have a strong probability to act as potential vaccine candidates. Nonetheless, it is imperative to subject these epitopes to further scientific examination both in vivo and in vitro, to confirm their suitability as vaccine candidates.

Authors

Institutions

Publication Details

Journal
IEEE Transactions on Artificial Intelligence
Published
2024-10-28
DOI
https://doi.org/10.1109/tai.2024.3487149
Citations
3
Primary Topic
Image Processing Techniques and Applications
Type
article
Field-Weighted Citation Impact
0.96
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Neural Network-Based Ensemble Learning Model to Identify Antigenic Fragments of SARS-CoV-2

Syed Nisar Hussain Bukhari, Kingsley A. Ogudo
3 citations
IEEE Transactions on Artificial Intelligence
Image Processing Techniques and Applications
0.96
article

Neural Network-Based Ensemble Learning Model to Identify Antigenic Fragments of SARS-CoV-2

Syed Nisar Hussain Bukhari, Kingsley A. Ogudo
article en
3 citations

Abstract

The development of epitope-based vaccines (EBVs) necessitates the identification of antigenic fragments (AFs) of the target pathogen known as T-cell epitopes (TCEs). TCEs are recognized by immune system, specifically by T cells, B cells, and antibodies. Traditional wet lab methods for identifying TCEs are often costly, challenging, and time-consuming compared to computational approaches. In this study, we propose a neural network-based ensemble machine learning (ML) model trained on physicochemical properties of SARS-CoV-2 peptides sequences to predict TCE sequences. The performance of the model assessed using test dataset demonstrated an accuracy of >95%, surpassing the results of other ML classifiers that were employed for comparative analysis. Through fivefold cross-validation technique, a mean accuracy of approximately 95% was reported. Additionally, when compared to other existing TCE prediction methods using a blind dataset, the proposed model was found to be more accurate and effective. The predicted epitopes may have a strong probability to act as potential vaccine candidates. Nonetheless, it is imperative to subject these epitopes to further scientific examination both in vivo and in vitro, to confirm their suitability as vaccine candidates.

IEEE Transactions on Artificial IntelligenceVol. 6(3)
University of Johannesburg (ZA), National Institute of Technology Srinagar (IN)
Openalex Percentile: Top 20%
Image Processing Techniques and Applications
0.96
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.