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Capacity-Approaching Constrained Codes With Error Correction for DNA-Based Data Storage

机译:容量接近基于DNA的数据存储纠错的受限代码

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摘要

We propose coding techniques that simultaneously limit the length of homopolymers runs, ensure the GC-content constraint, and are capable of correcting a single edit error in strands of nucleotides in DNA-based data storage systems. In particular, for given l, epsilon > 0, we propose simple and efficient encoders/decoders that transform binary sequences into DNA base sequences (codewords), namely sequences of the symbols A, T, C and G, that satisfy all of the following properties: 1) runlength constraint: the maximum homopolymer run in each codeword is at most l ; 2) GC-content constraint: the GC-content of each codeword is within [0.5- epsilon, 0.5+epsilon]; 3) error-correction: each codeword is capable of correcting a single deletion, or single insertion, or single substitution error. While various combinations of these properties have been considered in the literature, this work provides generalizations of codes constructions that satisfy all the properties with arbitrary parameters of l and epsilon. Furthermore, for practical values of l and epsilon, we show that our encoders achieve higher rates than existing results in the literature and approach capacity. Our methods have low encoding/decoding complexity and limited error propagation.
机译:我们提出了同时限制均聚物长度的编码技术,确保GC含量约束,并且能够在基于DNA的数据存储系统中校正核苷酸链中的单个编辑误差。特别地,对于给定L,epsilon> 0,我们提出简单且有效的编码器/解码器,其将二进制序列转化为DNA基本序列(码字),即符号A,T,C和G的序列,其满足以下所有内容属性:1)Runlength Constraint:每个码字中的最大均聚物最多为l; 2)GC含量约束:每个码字的GC含量在[0.5- epsilon,0.5 + epsilon]内; 3)纠错:每个码字都能够纠正单个删除或单个插入或单个替换错误。虽然在文献中考虑了这些性质的各种组合,但是该工作提供了满足L和epsilon任意参数的所有属性的代码结构的概括。此外,对于L和epsilon的实际价值,我们表明我们的编码器比文献和方法的现有结果实现更高的速率。我们的方法具有低编码/解码复杂性和有限的误差传播。

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