用酶合成纠正DNA数据存储中的缺失错误

Yuanyuan Tang, Farzad Farnoud
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引用次数: 2

摘要

DNA被认为是传统存储介质的一种很有前途的替代品,因为它具有数据密度高、寿命长和易于生成副本等优点。然而,DNA数据存储的主要缺点之一是DNA合成成本高且资源密集。一种新提出的酶促方法有可能降低合成成本,但缺点是不能精确控制碱基重复的次数。该方法也容易删除运行。这种合成方法的现有编码方法要么具有较低的速率,特别是每次运行$\leq\log_{2} 3$,要么不能防止删除错误。本文提出了一种新的纠错码和同步算法,可以对抗删除,并实现高于$\log_{2} 3$比特/单位时间的码率。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Correcting deletion errors in DNA data storage with enzymatic synthesis
DNA is considered a promising alternative to traditional storage media because of advantages such as high data density, longevity, and ease of generating copies. One of the major drawbacks of DNA data storage however is that DNA synthesis is costly and resource intensive. A newly proposed enzymatic method has the potential to decrease the cost of synthesis but has the disadvantage that the number of times a base is repeated cannot be precisely controlled. The method is also prone to deletion of runs. Existing encoding approaches for this synthesis method either have a low rate, specifically, $\leq\log_{2} 3$ per run, or cannot protect against deletion errors. The current paper proposes a new error-correcting code and a synchronization algorithm that can combat deletions and achieve a code rate higher than $\log_{2} 3$ bits per unit time.
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