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1.
Comput Intell Neurosci ; 2022: 8077664, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35875730

RESUMO

In the mid-1970s, the first-generation sequencing technique (Sanger) was created. It used Advanced BioSystems sequencing devices and Beckman's GeXP genetic testing technology. The second-generation sequencing (2GS) technique arrived just several years after the first human genome was published in 2003. 2GS devices are very quicker than Sanger sequencing equipment, with considerably cheaper manufacturing costs and far higher throughput in the form of short reads. The third-generation sequencing (3GS) method, initially introduced in 2005, offers further reduced manufacturing costs and higher throughput. Even though sequencing technique has result generations, it is error-prone due to a large number of reads. The study of this massive amount of data will aid in the decoding of life secrets, the detection of infections, the development of improved crops, and the improvement of life quality, among other things. This is a challenging task, which is complicated not just by a large number of reads and by the occurrence of sequencing mistakes. As a result, error correction is a crucial duty in data processing; it entails identifying and correcting read errors. Various k-spectrum-based error correction algorithms' performance can be influenced by a variety of characteristics like coverage depth, read length, and genome size, as demonstrated in this work. As a result, time and effort must be put into selecting acceptable approaches for error correction of certain NGS data.


Assuntos
Algoritmos , Sequenciamento de Nucleotídeos em Larga Escala , Sequenciamento de Nucleotídeos em Larga Escala/métodos , Humanos , Análise de Sequência de DNA
2.
J Healthc Eng ; 2022: 7528583, 2022.
Artigo em Inglês | MEDLINE | ID: mdl-35571336

RESUMO

Recently, with the availability of fast and reliable Internet, the distance between a patient and a doctor is becoming unimportant. Physicians will be able to request the medical images of their patients regardless of the geographical area. However, a lot of challenges face such successful implementation. To facilitate remote diagnosis, patient electronic medical record (EMR), including medical images, that originates in one system needs to be exchanged either within the same organization or across different organizations. Steganography is the practice of concealing a secret message inside a cover medium. In this paper, steganography will be used to embed the patient's personal information securely and imperceptibly in their medical images to enhance confidentiality in case of a distant diagnosis. The security of the medical data is improved to maintain confidentiality and integrity using IoT. The least significant bit of the approximate coefficient of integer wavelet transform is proposed. The distortion between the cover image and stego-image is obtained by measuring the mean square error and PSNR, and normalized cross-correlation is utilized to estimate the degree of closeness between the cover image and stego-image.


Assuntos
Segurança Computacional , Internet das Coisas , Algoritmos , Confidencialidade , Atenção à Saúde , Humanos
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