genomic signal
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2022 ◽  
Vol 9 (1) ◽  
Author(s):  
Emmanuel Adetiba ◽  
Joshua A. Abolarinwa ◽  
Anthony A. Adegoke ◽  
Tunmike B. Taiwo ◽  
Oluwaseun T. Ajayi ◽  
...  

Author(s):  
Safaa M Naeem ◽  
Mai S Mabrouk ◽  
Samir Y Marzouk ◽  
Mohamed A Eldosoky

Abstract Coronavirus Disease 2019 (COVID-19) is a sudden viral contagion that appeared at the end of last year in Wuhan city, the Chinese province of Hubei, China. The fast spread of COVID-19 has led to a dangerous threat to worldwide health. Also in the last two decades, several viral epidemics have been listed like the severe acute respiratory syndrome coronavirus (SARS-CoV) in 2002/2003, the influenza H1N1 in 2009 and recently the Middle East respiratory syndrome coronavirus (MERS-CoV) which appeared in Saudi Arabia in 2012. In this research, an automated system is created to differentiate between the COVID-19, SARS-CoV and MERS-CoV epidemics by using their genomic sequences recorded in the NCBI GenBank in order to facilitate the diagnosis process and increase the accuracy of disease detection in less time. The selected database contains 76 genes for each epidemic. Then, some features are extracted like a discrete Fourier transform (DFT), discrete cosine transform (DCT) and the seven moment invariants to two different classifiers. These classifiers are the k-nearest neighbor (KNN) algorithm and the trainable cascade-forward back propagation neural network where they give satisfying results to compare. To evaluate the performance of classifiers, there are some effective parameters calculated. They are accuracy (ACC), F1 score, error rate and Matthews correlation coefficient (MCC) that are 100%, 100%, 0 and 1, respectively, for the KNN algorithm and 98.89%, 98.34%, 0.0111 and 0.9754, respectively, for the cascade-forward network.


2019 ◽  
Vol 13 (2) ◽  
pp. 376-387 ◽  
Author(s):  
Belén Jiménez‐Mena ◽  
Alan Le Moan ◽  
Asbjørn Christensen ◽  
Mikael Deurs ◽  
Henrik Mosegaard ◽  
...  

2019 ◽  
Vol 98 ◽  
pp. 233-237 ◽  
Author(s):  
Dong-Wei Liu ◽  
Run-Ping Jia ◽  
Cai-Feng Wang ◽  
N. Arunkumar ◽  
K. Narasimhan ◽  
...  

2019 ◽  
Vol 9 (6) ◽  
pp. 1254-1261 ◽  
Author(s):  
Tao Shen ◽  
Yukari Nagai ◽  
M. Udayakumar ◽  
K. Narasimhan ◽  
R. K. Arvind Shriram ◽  
...  

Genomic signal processing (GSP) is the engineering discipline for the analysis, processing, and use of genomic signals to gain biological knowledge, and the translation of that knowledge into systems-based applications that can be used to diagnose and treat genetic diseases. Statistical Computations on DNA Sequences is one of key areas in which GSP can be applied. In this paper, we apply DSP tools on trinucleotide repeat disorders (too many copies of a certain nucleotide triplet in the DNA) to classify any gene sequence into diseased/non-diseased state. Intially, we collected the Gene sequences responsible for trinucleotide repeat disorders from NCBI. Then, we applied GSP techniques to convert the given gene sequence into an indicator sequence, and furthermore we apply Fast Fourier transforms (FFTs) and Discrete Wavelet Transforms (DWTs), followed by statistical feature extraction and the obtained statistical features, fed into an Artificial Neural Network to predict the state of the input genomic sequence.


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