DNA存储研究进展

Naveen Goela, J. Bolot
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引用次数: 0

摘要

随着DNA合成和测序成本的降低,超密集DNA存储是一种新兴的、可行的技术。最初的概念证明[1]-[3]已经产生了几个更大规模的实验,证明了DNA分子中的档案存储[4]-[7]。特别是,哈佛大学和Technicolor最近的合作宣布在合成DNA中存储了22mb的数据[4]。现有的存储系统主要使用高保真合成器。对于产生不可忽略的插入和缺失的合成器,产生的大部分寡核苷酸片段具有不等长的可变长度。本讲座概述了使用同步码(例如[8],[9])纠正变长段同步错误的方法。
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Advances in DNA storage
With decreasing costs for DNA synthesis and sequencing, ultra-dense DNA storage is an emerging, viable technology. The original proof of concept [1]–[3] has yielded several experiments of larger scale demonstrating archival storage in DNA molecules [4]–[7]. In particular, a recent collaboration by Harvard and Technicolor announced the storage of 22 MB of data in synthetic DNA [4]. Primarily, existing storage systems utilize high-fidelity synthesizers. For synthesizers which incur non-negligible insertions and deletions, a large fraction of the oligonucleotide segments produced have unequal, variable lengths. This talk overviews methods to correct for synchronization errors in variable-length segments using synchronization codes (e.g., [8], [9]).
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