English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Plus annual

Presents the access of premium content as premium feature

Premium Content

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools annual

Global: Zendy Free Plan

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Synthetic deoxyribonucleic acid (DNA) is a good medium for storing digital data for a long period due to its achievable high data storage density and outstanding longevity. However, synthesizing and sequencing DNA sequences in a DNA storage system are prone to a wide variety of errors, including insertion, deletion and mutation errors. At the same time, it is known that DNA sequences with 50&#x0025; GC content are less susceptible to errors. This paper presents the construction of a GC-balanced DNA sequence with error correction capability. A systematic single insertion/deletion/substitution error correction code is first proposed and then used to design a GC-balanced scheme for synthesizing DNA sequences. With the proposed method, DNA sequences with exactly 50&#x0025; GC content are constructed. Such DNA sequences not only have the maximum endurance to errors, but are able to correct both insertion/deletion and mutation of the nucleotide bases. The decoding procedures for the sequences are described and can readily be used in practice. Simulation results show that the proposed GC-balanced DNA sequences can correct base errors adequately.

ieee access

Notice of Violation of IEEE Publication Principles: Construction of GC-Balanced DNA With Deletion/Insertion/Mutation Error Correction for DNA Storage System