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Stream/Area:
-
Subject:
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Paper ID:
10.55041/IJSREM.RACCES094
Volume:
10 |
5 |
May 2026
Pages:
1-8
Publication Frequency:
Monthly (12 issues per year)
License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.
Computer Science & Engineering
Bharathiyar Institute of Engineering for women (Autonomous) Salem, TamilNadu, India
Computer Science & Engineering
Bharathiyar Institute of Engineering for women (Autonomous) Salem, TamilNadu, India
Cancer is one of the leading causes of mortality worldwide, and early detection is essential for improving survival rates and treatment outcomes. Conventional cancer diagnostic methods, such as tissue biopsies and imaging techniques, are often invasive, time-consuming, and costly. In recent years, liquid biopsy has emerged as a promising non-invasive alternative that enables the detection of cancer-related biomarkers from blood samples. Liquid biopsy techniques analyze biological components such as circulating tumor DNA (ctDNA), circulating tumor cells (CTCs), and other molecular signals present in body fluids. However, the biological data generated from liquid biopsies are highly complex and require advanced computational methods to accurately interpret patterns associated with different cancer types. This study proposes an end-to-end deep neural network (DNN) model for cancer type classification using liquid biopsy data. The proposed approach directly processes raw molecular data and automatically learns meaningful feature representations without the need for extensive manual feature engineering. By leveraging the capability of deep learning to model complex biological relationships, the system identifies patterns that distinguish different cancer types with high accuracy. The end-to-end architecture enables efficient feature extraction, pattern learning, and classification within a unified framework. The proposed model aims to assist clinicians in the early detection and accurate classification of cancer, thereby supporting more effective diagnosis, personalized treatment planning, and improved patient outcomes.
KEYWORDS
In this research, an End-to-End Deep Neural Network model was proposed for cancer type classification using liquid biopsy data. The system integrates multiple modules including data collection, preprocessing, feature extraction, deep neural network modeling, and classification within a unified framework. By directly processing raw genomic and molecular biomarker data, the proposed architecture eliminates the need for manual feature engineering and enables automatic learning of meaningful patterns associated with different cancer types. The experimental results demonstrate that the proposed model can accurately classify multiple cancer types with improved performance compared to traditional machine learning methods. The deep neural network successfully learns complex relationships within high-dimensional biomedical data and provides reliable predictions for cancer diagnosis. In addition, the use of regularization techniques and optimized training strategies improves the model’s generalization ability and reduces overfitting. The system offers a scalable and efficient solution for analyzing liquid biopsy data and supporting clinicians in early cancer detection and diagnosis. Although the proposed approach shows promising results, there are several opportunities for further research and improvement. Future work may focus on integrating additional biological data sources such as gene expression profiles, proteomic data, and clinical patient information to enhance the model’s predictive capability. Advanced deep learning architectures such as transformer-based models and attention mechanisms can also be explored to further improve classification accuracy. In addition, implementing the system in real-time clinical decision support platforms could help healthcare professionals perform faster and more accurate cancer diagnosis. Expanding the model to detect early-stage cancers and rare cancer types using large-scale biomedical datasets will also be an important direction for future research.
[1] Cherukuri, S. P., Kaur, A., Goyal, B., Kukunoor, H. R., Sahito, A. F., Sachdeva, P., et al., “Artificial Intelligence-Enhanced Liquid Biopsy and Radiomics in Early-Stage Lung Cancer Detection,” Cancers, vol. 17, no. 19, 2025. [2] Luo, X., Xie, S., Hong, F., Li, X., Wei, Y., Zhou, Y., et al., “From multi-omics to deep learning: Advances in cfDNA-based liquid biopsy for multi-cancer screening,” Biomarker Research, 2025. [3] Li, L., Geng, Y., Chen, T., et al., “Deep learning model targeting cancer surrounding tissues for accurate cancer diagnosis,” Journal of Translational Medicine, vol. 23, 2025. [4] Shao, X., Shen, Y., Sun, P., et al., “Real-time deep learning for tumor segmentation and tool tracking in breast biopsy,” World Journal of Surgical Oncology, 2025. [5] Eledkawy, A., Hamza, T., & El-Metwally, S., “Precision cancer classification using liquid biopsy and advanced machine learning techniques,” Scientific Reports, 2024. [6] Guerry, J., “Recent advances in liquid biopsy for precision oncology and clinical applications in lung cancer,” Future Oncology, 2025. [7] Mishra, A. K., Alrubayan, M., & Pradhan, P., “Automated grading and staging of ovarian cancer using deep learning,” arXiv, 2025. [8] Zang, Z., Dorward, D. A., Quiohilag, K. E., et al., “Deep learning-based pathological subtyping of non-small cell lung cancer,” arXiv, 2025. [9] Sarfati, E., Bône, A., Rohé, M., et al., “Deep learning-based classification of hepatocellular carcinoma using CT scans,” arXiv, 2025. [10] Di Caro, G., Kirakosyan, V., Abanov, A. G., et al., “Quantum cognition machine learning for forecasting chromosomal instability,” arXiv, 2025.
Publication Date
5/8/2026
Peer Review Type
Double-Blind Peer Review
Review Rounds: 2
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The authors declare no conflict of interest related to this research work.
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