The Capacity of Secondary Structure Avoidance Codes for DNA Sequences

IF 2.4 Q2 ENGINEERING, ELECTRICAL & ELECTRONIC IEEE Transactions on Molecular, Biological, and Multi-Scale Communications Pub Date : 2024-03-03 DOI:10.1109/TMBMC.2024.3396404
Chen Wang;Hui Chu;Gennian Ge;Yiwei Zhang
{"title":"The Capacity of Secondary Structure Avoidance Codes for DNA Sequences","authors":"Chen Wang;Hui Chu;Gennian Ge;Yiwei Zhang","doi":"10.1109/TMBMC.2024.3396404","DOIUrl":null,"url":null,"abstract":"In DNA sequences, we have the celebrated Watson-Crick complement \n<inline-formula> <tex-math>$\\overline {T}=A, \\overline {A}=T, \\overline {C}=G$ </tex-math></inline-formula>\n, and \n<inline-formula> <tex-math>$\\overline {G}=C$ </tex-math></inline-formula>\n. The phenomenon of secondary structure refers to the tendency of a single stranded DNA sequence to fold back upon itself, which is usually caused by the existence of two non-overlapping reverse complement substrings. The property of secondary structure avoidance (SSA) forbids a sequence to contain such reverse complement substrings, and it is a key criterion in the design of single-stranded DNA sequences for both DNA storage and DNA computing. In this paper, we prove that the problem of constructing SSA sequences for any given secondary structure stem length \n<italic>m</i>\n can be characterized by a constrained system, and thus the capacity of SSA sequences can be calculated by the classic spectral radius approach in constrained coding theory. We analyze how to choose the generating set, which is a subset of vertices in a de Bruijn graph, for the constrained system, which leads to some explicit constructions of SSA codes. In particular, our constructions have optimal rates 1.1679bits/nt and 1.5515bits/nt when \n<inline-formula> <tex-math>${m} = 2$ </tex-math></inline-formula>\n and \n<inline-formula> <tex-math>${m} = 3$ </tex-math></inline-formula>\n, respectively. In addition, we combine the SSA constraint together with the homopolymer run-length-limit constraint and analyze the capacity of sequences satisfying both constraints.","PeriodicalId":36530,"journal":{"name":"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications","volume":null,"pages":null},"PeriodicalIF":2.4000,"publicationDate":"2024-03-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"IEEE Transactions on Molecular, Biological, and Multi-Scale Communications","FirstCategoryId":"1085","ListUrlMain":"https://ieeexplore.ieee.org/document/10517954/","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, ELECTRICAL & ELECTRONIC","Score":null,"Total":0}
引用次数: 0

Abstract

In DNA sequences, we have the celebrated Watson-Crick complement $\overline {T}=A, \overline {A}=T, \overline {C}=G$ , and $\overline {G}=C$ . The phenomenon of secondary structure refers to the tendency of a single stranded DNA sequence to fold back upon itself, which is usually caused by the existence of two non-overlapping reverse complement substrings. The property of secondary structure avoidance (SSA) forbids a sequence to contain such reverse complement substrings, and it is a key criterion in the design of single-stranded DNA sequences for both DNA storage and DNA computing. In this paper, we prove that the problem of constructing SSA sequences for any given secondary structure stem length m can be characterized by a constrained system, and thus the capacity of SSA sequences can be calculated by the classic spectral radius approach in constrained coding theory. We analyze how to choose the generating set, which is a subset of vertices in a de Bruijn graph, for the constrained system, which leads to some explicit constructions of SSA codes. In particular, our constructions have optimal rates 1.1679bits/nt and 1.5515bits/nt when ${m} = 2$ and ${m} = 3$ , respectively. In addition, we combine the SSA constraint together with the homopolymer run-length-limit constraint and analyze the capacity of sequences satisfying both constraints.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
DNA 序列二级结构规避代码的能力
在 DNA 序列中,我们有著名的沃森-克里克补码 $/overline {T}=A, \overline {A}=T, \overline {C}=G$ 和 $/overline {G}=C$ 。二级结构现象指的是单链 DNA 序列折回自身的趋势,这通常是由于存在两个非重叠的反向互补子串造成的。避免二级结构(SSA)的特性禁止序列包含这种反向互补子串,它是设计用于 DNA 存储和 DNA 计算的单链 DNA 序列的关键标准。本文证明,对于任意给定的二级结构茎长度 m,构建 SSA 序列的问题可以用一个约束系统来表征,因此 SSA 序列的容量可以用约束编码理论中经典的谱半径方法来计算。我们分析了如何为约束系统选择生成集(即 de Bruijn 图中的顶点子集),从而得出一些 SSA 编码的明确构造。特别是,当 ${m} = 2$ 和 ${m} = 3$ 时,我们的构造分别具有 1.1679bits/nt 和 1.5515bits/nt 的最佳速率。此外,我们还结合了 SSA 约束和同源多聚物运行长度限制约束,并分析了满足这两个约束的序列的容量。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
CiteScore
3.90
自引率
13.60%
发文量
23
期刊介绍: As a result of recent advances in MEMS/NEMS and systems biology, as well as the emergence of synthetic bacteria and lab/process-on-a-chip techniques, it is now possible to design chemical “circuits”, custom organisms, micro/nanoscale swarms of devices, and a host of other new systems. This success opens up a new frontier for interdisciplinary communications techniques using chemistry, biology, and other principles that have not been considered in the communications literature. The IEEE Transactions on Molecular, Biological, and Multi-Scale Communications (T-MBMSC) is devoted to the principles, design, and analysis of communication systems that use physics beyond classical electromagnetism. This includes molecular, quantum, and other physical, chemical and biological techniques; as well as new communication techniques at small scales or across multiple scales (e.g., nano to micro to macro; note that strictly nanoscale systems, 1-100 nm, are outside the scope of this journal). Original research articles on one or more of the following topics are within scope: mathematical modeling, information/communication and network theoretic analysis, standardization and industrial applications, and analytical or experimental studies on communication processes or networks in biology. Contributions on related topics may also be considered for publication. Contributions from researchers outside the IEEE’s typical audience are encouraged.
期刊最新文献
Table of Contents IEEE Transactions on Molecular, Biological, and Multi-Scale Communications Publication Information Guest Editorial Introduction to the Special Feature on the 8th Workshop on Molecular Communications Guest Editorial Special Feature on Seeing Through the Crowd: Molecular Communication in Crowded and Multi-Cellular Environments IEEE Communications Society Information
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1