A Non-invasive Cell-free DNA Diagnosis Method for Hepatocellular Carcinoma Based on Deep Learning

被引:0
|
作者
Li, Xueyi [1 ]
Zhang, Wei [1 ]
Liu, Zhi-Ping [1 ]
机构
[1] Shandong Univ, Sch Control Sci & Engn, Dept Biomed Engn, Jinan 250061, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Hepatocellular carcinoma; DNA methylation; cfDNA; low sequencing depths; biomarker discovery; deep learning; METHYLATION; SERUM;
D O I
10.2174/0115748936334029250213041916
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background Hepatocellular Carcinoma (HCC) is a major disease that seriously threatens human health. Early screening can significantly improve the five-year survival rate of HCC patients. Cell-free DNA (cfDNA), as a potential carrier of cancer signals in body fluids, can be used for early cancer detection. However, current early HCC detection methods based on cfDNA sequencing require deep sequencing data, limiting their application and usage in routine disease screening.Objective We proposed a foundational DNA language model, called CLHCC, for analyzing DNA sequences and methylation patterns to detect HCC at low sequencing depths.Methods CLHCC randomly selected 1500 DNA fragments from HCC-specific differentially methylated regions identified by cd-score. The model then performed a one-hot encoding strategy on these DNA fragments and input the data into a CNN combined with an LSTM neural network for classification.Results We tested CLHCC on 2139 target-BS data samples, achieving an accuracy of 84.59% (precision: 83.44%, recall: 81%) under 10-fold cross-validations. This performance is better than DNA language models built using CNN or LSTM alone.Conclusion Our study applies deep learning to analyze DNA sequences in specific methylation regions without the need for complex alignment processes. This provides new theoretical and practical guidance for clinical applications and holds promise for non-invasive early HCC screening via cfDNA.
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页数:10
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