Notice of Violation of IEEE Publication Principles"Construction of GC-Balanced DNA With Deletion/Insertion/Mutation Error Correction for DNA Storage System,"by Tianbo Xue and Francis Lauin IEEE Access, vol. 8, pp. 140972-140980, 2020After careful and considered review of the content and authorship of this paper by a duly constituted expert committee, this paper has been found to be in violation of IEEE’s Publication Principles.This paper contains significant portions of text from the paper cited below that were reused without attribution.“Linear-Time Encoders for Codes Correcting a Single Edit for DNA-Based Data Storages”by Y. M. Chee, H. M. Kiah, and T. T. Nguyen,in the Proceedings of the IEEE International Symposium on Information Theory (ISIT), Jul. 2019.“Optimal Codes Correcting a Single Indel / Edit for DNA-Based Data Storage”by K. Cai, Y. M. Chee, R. Gabrys, H. M. Kiah, and T. T. Nguyenin arXiv, arXiv:1910.06501, Oct. 2019.Synthetic deoxyribonucleic acid (DNA) is a good medium for storing digital data for a long period due to its achievable high data storage density and outstanding longevity. However, synthesizing and sequencing DNA sequences in a DNA storage system are prone to a wide variety of errors, including insertion, deletion and mutation errors. At the same time, it is known that DNA sequences with 50% GC content are less susceptible to errors. This paper presents the construction of a GC-balanced DNA sequence with error correction capability. A systematic single insertion/deletion/substitution error correction code is first proposed and then used to design a GC-balanced scheme for synthesizing DNA sequences. With the proposed method, DNA sequences with exactly 50% GC content are constructed. Such DNA sequences not only have the maximum endurance to errors, but are able to correct both insertion/deletion and mutation of the nucleotide bases. The decoding procedures for the sequences are described and can readily be used in practice. Simulation results show that the proposed GC-balanced DNA sequences can correct base errors adequately.

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违反 IEEE 出版原则的通知“为 DNA 存储系统构建具有删除/插入/突变纠错功能的 GC 平衡 DNA”，作者：Tianbo Xu 和 Francis Lauin IEEE Access，第 1 卷。 8，第 140972-140980 页，2020 经过正式组建的专家委员会对本文的内容和作者进行仔细和深思熟虑的审查后，发现本文违反了 IEEE 的出版原则。本文包含来自下面引用的论文在未注明出处的情况下被重复使用。“用于纠正基于 DNA 的数据存储的单一编辑的代码的线性时间编码器”作者：YM Chee、HM Kiah 和 TT Nguyen，发表于 IEEE 国际信息论研讨会论文集(ISIT)，2019 年 7 月。“针对基于 DNA 的数据存储纠正单个插入/编辑的最佳代码”作者：K. Cai、YM Chee、R. Gabrys、HM Kiah 和 TT Nguyenin arXiv，arXiv：1910.06501，10 月 19 日2019.合成脱氧核糖核酸（DNA）由于其可实现的高数据存储密度和出色的寿命而成为长期存储数字数据的良好介质。然而，在 DNA 存储系统中合成和测序 DNA 序列很容易出现各种错误，包括插入、删除和突变错误。同时，众所周知，GC 含量为 50% 的 DNA 序列不易出错。本文介绍了具有纠错能力的 GC 平衡 DNA 序列的构建。首先提出了系统的单插入/删除/替换纠错码，然后用于设计用于合成DNA序列的GC平衡方案。通过所提出的方法，构建了 GC 含量恰好为 50% 的 DNA 序列。 这样的DNA序列不仅具有最大的容错能力，而且能够纠正核苷酸碱基的插入/缺失和突变。描述了序列的解码过程并且可以很容易地在实践中使用。模拟结果表明，所提出的GC平衡DNA序列可以充分纠正碱基错误。