Prediction of exosomal miRNA-based biomarkers for liquid biopsy

In this study, we investigated the properties of exosomal miRNAs to identify potential biomarkers for liquid biopsy. We collected 956 exosomal and 956 non-exosomal miRNA sequences from RNALocate and miRBase to develop predictive models. Our initial analysis reveals that specific nucleotides are preferred at certain positions in miRNAs associated with exosomes. We employed an alignment-based approach, artificial intelligence (AI) models, and ensemble methods for predicting exosomal miRNAs. For the alignment-based approach, we used a motif-based method with MERCI and a similarity-based method with BLAST, achieving high precision but low coverage of about 29%. The AI models, developed using machine learning, deep learning techniques, and pretrained language models, achieved a maximum AUC of 0.707 and an MCC of 0.268 on an independent dataset. Finally, our ensemble method, combining alignment-based and AI-based models, reached a maximum AUC of 0.73 and an MCC of 0.352 on an independent dataset. We have developed a web server, EmiRPred, to assist the scientific community in predicting and designing exosomal miRNAs and identifying associated motifs ( https://webs.iiitd.edu.in/raghava/emirpred/ ).

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Publication Details

Journal
Scientific Reports
Published
2025-08-25
DOI
https://doi.org/10.1038/s41598-025-15814-y
Citations
3
Primary Topic
Extracellular vesicles in disease
Type
article
Field-Weighted Citation Impact
2.42

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article

Prediction of exosomal miRNA-based biomarkers for liquid biopsy

Gajendra P. S. Raghava, Akanksha Arora
3 citations
Scientific Reports
Extracellular vesicles in disease
2.42
article

Prediction of exosomal miRNA-based biomarkers for liquid biopsy

Gajendra P. S. Raghava, Akanksha Arora
article en
3 citations

Abstract

In this study, we investigated the properties of exosomal miRNAs to identify potential biomarkers for liquid biopsy. We collected 956 exosomal and 956 non-exosomal miRNA sequences from RNALocate and miRBase to develop predictive models. Our initial analysis reveals that specific nucleotides are preferred at certain positions in miRNAs associated with exosomes. We employed an alignment-based approach, artificial intelligence (AI) models, and ensemble methods for predicting exosomal miRNAs. For the alignment-based approach, we used a motif-based method with MERCI and a similarity-based method with BLAST, achieving high precision but low coverage of about 29%. The AI models, developed using machine learning, deep learning techniques, and pretrained language models, achieved a maximum AUC of 0.707 and an MCC of 0.268 on an independent dataset. Finally, our ensemble method, combining alignment-based and AI-based models, reached a maximum AUC of 0.73 and an MCC of 0.352 on an independent dataset. We have developed a web server, EmiRPred, to assist the scientific community in predicting and designing exosomal miRNAs and identifying associated motifs ( https://webs.iiitd.edu.in/raghava/emirpred/ ).

Scientific ReportsVol. 15(1)
Indraprastha Institute of Information Technology Delhi (IN)
Department of Biotechnology, Ministry of Science and Technology, India, Council of Scientific and Industrial Research, India, Indian Institute of Technology Delhi
Openalex Percentile: Top 10%
Extracellular vesicles in disease
2.42
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