Managing reliability skew in DNA storage

Dehui Lin, Yasamin Tabatabaee, Yash Pote, Djordje Jevdjic
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引用次数: 4

Abstract

DNA is emerging as an increasingly attractive medium for data storage due to a number of important and unique advantages it offers, most notably the unprecedented durability and density. While the technology is evolving rapidly, the prohibitive cost of reads and writes, the high frequency and the peculiar nature of errors occurring in DNA storage pose a significant challenge to its adoption. In this work we make a novel observation that the probability of successful recovery of a given bit from any type of a DNA-based storage system highly depends on its physical location within the DNA molecule. In other words, when used as a storage medium, some parts of DNA molecules appear significantly more reliable than others. We show that large differences in reliability between different parts of DNA molecules lead to highly inefficient use of error-correction resources, and that commonly used techniques such as unequal error-correction cannot be used to bridge the reliability gap between different locations in the context of DNA storage. We then propose two approaches to address the problem. The first approach is general and applies to any types of data; it stripes the data and ECC codewords across DNA molecules in a particular fashion such that the effects of errors are spread out evenly across different codewords and molecules, effectively de-biasing the underlying storage medium and improving the resilience against losses of entire molecules. The second approach is application-specific, and seeks to leverage the underlying reliability bias by using application-aware mapping of data onto DNA molecules such that data that requires higher reliability is stored in more reliable locations, whereas data that needs lower reliability is stored in less reliable parts of DNA molecules. We show that the proposed data mapping can be used to achieve graceful degradation in the presence of high error rates, or to implement the concept of approximate storage in DNA. All proposed mechanisms are seamlessly integrated into the state-of-the art DNA storage pipeline at zero storage overhead, validated through wetlab experiments, and evaluated on end-to-end encrypted and compressed data.
管理DNA存储的可靠性偏差
DNA正成为越来越有吸引力的数据存储介质,因为它提供了许多重要和独特的优势,最显著的是前所未有的耐用性和密度。虽然这项技术正在迅速发展,但读取和写入的高昂成本、DNA存储中发生错误的高频率和特殊性质对其采用构成了重大挑战。在这项工作中,我们提出了一个新的观察,即从任何类型的基于DNA的存储系统中成功恢复给定比特的概率高度依赖于其在DNA分子中的物理位置。换句话说,当用作存储介质时,DNA分子的某些部分明显比其他部分更可靠。我们表明,DNA分子不同部分之间的可靠性差异导致错误纠正资源的使用效率极低,并且通常使用的技术,如不等错误纠正,不能用于弥合DNA存储背景下不同位置之间的可靠性差距。然后我们提出两种方法来解决这个问题。第一种方法是通用的,适用于任何类型的数据;它以一种特殊的方式在DNA分子上分割数据和ECC码字,使错误的影响均匀地分布在不同的码字和分子上,有效地消除了底层存储介质的偏置,提高了抵御整个分子损失的弹性。第二种方法是特定于应用程序的,并通过使用应用程序感知的数据到DNA分子的映射来寻求利用潜在的可靠性偏差,这样需要更高可靠性的数据存储在更可靠的位置,而需要较低可靠性的数据存储在DNA分子的不太可靠的部分。我们表明,所提出的数据映射可以用于在高错误率的情况下实现优雅的退化,或者实现DNA中的近似存储概念。所有提出的机制都以零存储开销无缝集成到最先进的DNA存储管道中,通过湿实验室实验进行验证,并对端到端加密和压缩数据进行评估。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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