一种基于DNA序列和数学函数的安全指纹隐藏技术
Wala'a Essa Al-Ahmadi1, Asia Othman Aljahdali2, Fursan Thabit3
1Computer Science and Artificial Intelligence Department, College of Computer Science and Engineering, University of Jeddah, Jeddah, Saudi Arabia.
PeerJ. Computer science
|April 25, 2024
概括
这项研究引入了一种新的DNA隐藏法方法,可在DNA序列中安全嵌入加密的指纹图像. 该技术增强了生物识别数据的安全性,防止未经授权的访问和攻击.
科学领域:
- 生物技术是生物技术.
- 密码学 密码学 密码学 密码学
- 数据安全 数据安全
背景情况:
- 生物识别数据,如指纹,由于其永久性,需要强大的安全性.
- 现有的数据传输方法对敏感的生物识别信息缺乏足够的安全性.
- DNA 隐藏图提供了一种新的方法来安全嵌入数据.
研究的目的:
- 开发一种安全的技术,将DNA隐形图和密码学结合起来,用于指纹图像保护.
- 在通信过程中增强生物识别数据的机密性和完整性.
- 为了创建一种强大的方法,可以抵抗常见的加密分析攻击.
主要方法:
- 指纹图像转换为二进制数据,然后使用Feistel网络加密.
- 用专门的插入技术嵌入到DNA序列中的加密数据.
- 采用四个随机键来增强安全性和一个大的钥匙空间.
主要成果:
- 拟议的方法证明了高安全性,破裂概率低.
- 实现了高效的执行时间和大量的数据隐藏位置.
- 该技术被证明能够抵御已知的纯文本和选择的纯文本攻击,并通过NIST测试进行验证.
结论:
- 开发的DNA隐形图像技术在传输过程中有效地保护指纹图像.
- 隐形图和加密图的结合提供了对数据泄露的强有力的防御.
- 限制包括无法处理大型文件,限制其使用到小图像.
相关概念视频
Sanger Sequencing
754.1K
DNA sequencing is a fundamental technique that is routinely used in the biological sciences. This method can be applied to a range of questions at different scales - from the sequencing of a cloned DNA fragment or the study of a mutation in a gene up to whole-genome sequencing. However, despite the widespread use of sequencing today, it was not until 1977 that Fredrick Sanger and his collaborators developed the chain-termination method to decode DNA sequences. It relies on the separation of a...
754.1K
Maxam-Gilbert Sequencing
11.2K
In the same year as the discovery of the Sanger sequencing method, another group of scientists, Allan Maxam and Walter Gilbert, demonstrated their chemical-cleavage method for DNA sequencing. The Maxam-Gilbert method relies on using different chemicals that can cleave the DNA sequence at specific sites, the separation of resulting DNA fragments of variable size using electrophoresis, and deciphering the DNA sequence from the resulting gel bands.
Challenges of the Maxam-Gilbert Method
The...
Challenges of the Maxam-Gilbert Method
The...
11.2K
DNA as a Genetic Template
21.9K
Two structural features of the DNA molecule provide a basis for the mechanisms of heredity: the four nucleotide bases and its double-stranded nature. The Watson-Crick model of double-helical DNA structure, proposed in 1952, drew heavily upon the X-ray crystallography work of researchers Rosalind Franklin and Maurice Wilkins. Watson, Crick, and Wilkins jointly received the Nobel Prize in Physiology or Medicine for their work in 1962. Franklin was, controversially, excluded from the prize for...
21.9K
Single-Strand DNA Binding Proteins
14.1K
For successful DNA replication, the unwinding of double-stranded DNA must be accompanied by stabilization and protection of the separated single strands of the DNA. This crucial task is performed by single-strand DNA-binding (SSB) proteins. They bind to the DNA in a sequence-independent manner, which means that the nitrogenous bases of the DNA need not be present in a specific order for binding of SSB proteins to it. The binding of SSB proteins straightens single-stranded DNA (ssDNA) and makes...
14.1K
Evolutionary Relationships through Genome Comparisons
5.7K
Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
5.7K
Southern Blot
19.3K
Agarose gel electrophoresis is very useful in separating DNA fragments by size. Running a DNA ladder containing fragments of the known length alongside the sample helps determine the approximate length of the sample DNA fragments. However, additional steps are needed to verify the sequence identity of the sample DNA fragments.
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
Denatured DNA fragments must be transferred onto a carrier membrane from the gel to make it accessible to a probe - a small ssDNA fragment complementary to the target DNA...
19.3K


