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Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome using MEGA
The novel coronavirus pandemic that has originated from China and spread throughout the world in three months. Genome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) predecessor, severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Korea Genome Organization
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560444/ https://www.ncbi.nlm.nih.gov/pubmed/33017874 http://dx.doi.org/10.5808/GI.2020.18.3.e30 |
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author | Sohpal, Vipan Kumar |
author_facet | Sohpal, Vipan Kumar |
author_sort | Sohpal, Vipan Kumar |
collection | PubMed |
description | The novel coronavirus pandemic that has originated from China and spread throughout the world in three months. Genome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) predecessor, severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) play an important role in understanding the concept of genetic variation. In this paper, the genomic data accessed from National Center for Biotechnology Information (NCBI) through Molecular Evolutionary Genetic Analysis (MEGA) for statistical analysis. Firstly, the Bayesian information criterion (BIC) and Akaike information criterion (AICc) are used to evaluate the best substitution pattern. Secondly, the maximum likelihood method used to estimate of transition/transversions (R) through Kimura-2, Tamura-3, Hasegawa-Kishino-Yano, and Tamura-Nei nucleotide substitutions model. Thirdly and finally nucleotide frequencies computed based on genomic data of NCBI. The results indicate that general times reversible model has the lowest BIC and AICc score 347,394 and 347,287, respectively. The transition/transversions bias for nucleotide substitutions models varies from 0.56 to 0.59 in MEGA output. The average nitrogenous bases frequency of U, C, A, and G are 31.74, 19.48, 28.04, and 20.74, respectively in percentages. Overall the genomic data analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV highlights the close genetic relationship. |
format | Online Article Text |
id | pubmed-7560444 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Korea Genome Organization |
record_format | MEDLINE/PubMed |
spelling | pubmed-75604442020-10-21 Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome using MEGA Sohpal, Vipan Kumar Genomics Inform Original Article The novel coronavirus pandemic that has originated from China and spread throughout the world in three months. Genome of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) predecessor, severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle East respiratory syndrome coronavirus (MERS-CoV) play an important role in understanding the concept of genetic variation. In this paper, the genomic data accessed from National Center for Biotechnology Information (NCBI) through Molecular Evolutionary Genetic Analysis (MEGA) for statistical analysis. Firstly, the Bayesian information criterion (BIC) and Akaike information criterion (AICc) are used to evaluate the best substitution pattern. Secondly, the maximum likelihood method used to estimate of transition/transversions (R) through Kimura-2, Tamura-3, Hasegawa-Kishino-Yano, and Tamura-Nei nucleotide substitutions model. Thirdly and finally nucleotide frequencies computed based on genomic data of NCBI. The results indicate that general times reversible model has the lowest BIC and AICc score 347,394 and 347,287, respectively. The transition/transversions bias for nucleotide substitutions models varies from 0.56 to 0.59 in MEGA output. The average nitrogenous bases frequency of U, C, A, and G are 31.74, 19.48, 28.04, and 20.74, respectively in percentages. Overall the genomic data analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV highlights the close genetic relationship. Korea Genome Organization 2020-09-24 /pmc/articles/PMC7560444/ /pubmed/33017874 http://dx.doi.org/10.5808/GI.2020.18.3.e30 Text en (c) 2020, Korea Genome Organization (CC) This is an open-access article distributed under the terms of the Creative Commons Attribution license(https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Sohpal, Vipan Kumar Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome using MEGA |
title | Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome
using MEGA |
title_full | Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome
using MEGA |
title_fullStr | Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome
using MEGA |
title_full_unstemmed | Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome
using MEGA |
title_short | Computational analysis of SARS-CoV-2, SARS-CoV, and MERS-CoV genome
using MEGA |
title_sort | computational analysis of sars-cov-2, sars-cov, and mers-cov genome
using mega |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560444/ https://www.ncbi.nlm.nih.gov/pubmed/33017874 http://dx.doi.org/10.5808/GI.2020.18.3.e30 |
work_keys_str_mv | AT sohpalvipankumar computationalanalysisofsarscov2sarscovandmerscovgenomeusingmega |