Deep Joint Source-Channel Coding for DNA Image Storage: A Novel Approach With Enhanced Error Resilience and Biological Constraint Optimization

IF 2.4 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC IEEE Transactions on Molecular, Biological, and Multi-Scale Communications Pub Date : 2023-11-09 DOI:10.1109/TMBMC.2023.3331579
Wenfeng Wu;Luping Xiang;Qiang Liu;Kun Yang
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Abstract

In the current era, DeoxyriboNucleic Acid (DNA) based data storage emerges as an intriguing approach, garnering substantial academic interest and investigation. This paper introduces a novel deep joint source-channel coding (DJSCC) scheme for DNA image storage, designated as DJSCC-DNA. This paradigm distinguishes itself from conventional DNA storage techniques through three key modifications: 1) it employs advanced deep learning methodologies, employing convolutional neural networks for DNA encoding and decoding processes; 2) it seamlessly integrates DNA polymerase chain reaction (PCR) amplification into the network architecture, thereby augmenting data recovery precision; and 3) it restructures the loss function by targeting biological constraints for optimization. The performance of the proposed model is demonstrated via numerical results from specific channel testing, suggesting that it surpasses conventional deep learning methodologies in terms of peak signal-to-noise ratio (PSNR) and structural similarity index (SSIM). Additionally, the model effectively ensures positive constraints on both homopolymer run-length and GC content.
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用于 DNA 图像存储的深度源-信道联合编码:增强抗错能力和生物约束优化的新方法
当今时代,基于脱氧核糖核酸(DNA)的数据存储成为一种引人入胜的方法,引起了学术界的极大兴趣和研究。本文介绍了一种用于 DNA 图像存储的新型深度联合源信道编码(DJSCC)方案,命名为 DJSCC-DNA。该范例通过三个关键修改将自己与传统的 DNA 存储技术区分开来:1)它采用了先进的深度学习方法,在 DNA 编码和解码过程中使用卷积神经网络;2)它将 DNA 聚合酶链式反应(PCR)扩增无缝集成到网络架构中,从而提高了数据恢复精度;3)它通过针对生物约束进行优化来重组损失函数。通过特定信道测试的数值结果证明了所提模型的性能,表明它在峰值信噪比(PSNR)和结构相似性指数(SSIM)方面超越了传统的深度学习方法。此外,该模型还有效地确保了对均聚物运行长度和 GC 含量的正向约束。
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来源期刊
CiteScore
3.90
自引率
13.60%
发文量
23
期刊介绍: As a result of recent advances in MEMS/NEMS and systems biology, as well as the emergence of synthetic bacteria and lab/process-on-a-chip techniques, it is now possible to design chemical “circuits”, custom organisms, micro/nanoscale swarms of devices, and a host of other new systems. This success opens up a new frontier for interdisciplinary communications techniques using chemistry, biology, and other principles that have not been considered in the communications literature. The IEEE Transactions on Molecular, Biological, and Multi-Scale Communications (T-MBMSC) is devoted to the principles, design, and analysis of communication systems that use physics beyond classical electromagnetism. This includes molecular, quantum, and other physical, chemical and biological techniques; as well as new communication techniques at small scales or across multiple scales (e.g., nano to micro to macro; note that strictly nanoscale systems, 1-100 nm, are outside the scope of this journal). Original research articles on one or more of the following topics are within scope: mathematical modeling, information/communication and network theoretic analysis, standardization and industrial applications, and analytical or experimental studies on communication processes or networks in biology. Contributions on related topics may also be considered for publication. Contributions from researchers outside the IEEE’s typical audience are encouraged.
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Table of Contents IEEE Transactions on Molecular, Biological, and Multi-Scale Communications Publication Information Guest Editorial Introduction to the Special Feature on the 8th Workshop on Molecular Communications Guest Editorial Special Feature on Seeing Through the Crowd: Molecular Communication in Crowded and Multi-Cellular Environments IEEE Communications Society Information
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