tetano
Editor, Senior Moderator
Infect Genet Evol
. 2020 Sep 1;104522.
doi: 10.1016/j.meegid.2020.104522. Online ahead of print.
Inferring the genetic variability in Indian SARS-CoV-2 genomes using consensus of multiple sequence alignment techniques
Indrajit Saha[SUP] 1 [/SUP], Nimisha Ghosh[SUP] 2 [/SUP], Debasree Maity[SUP] 3 [/SUP], Nikhil Sharma[SUP] 4 [/SUP], Kaushik Mitra[SUP] 5 [/SUP]
Affiliations
Abstract
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is a threat to the human population and has created a worldwide pandemic. Daily thousands of people are getting affected by the SARS-CoV-2 virus; India being no exception. In this situation, there is no doubt that vaccine is the primary prevention strategy to contain the wave of COVID-19 pandemic. In this regard, genome-wide analysis of SARS-CoV-2 is important to understand its genetical variability. This has motivated us to analyse the 566 Indian SARS-CoV-2 sequences using multiple sequence alignment techniques viz. ClustalW, MUSCLE, ClustalO and MAFFT to identify the lists of mutations as substitution, deletion, insertion and SNP. Thereafter, a consensus of these results, called as Consensus Multiple Sequence Alignment (CMSA), is considered to have the final list of mutations so that the advantages of all four alignment techniques can be preserved. The analysis shows 767, 2025 and 54 unique substitutions, deletions and SNPs in Indian SARS-CoV-2 genomes. More precisely, out of 54 SNPs, 4 SNPs are present close to the 60% of the virus population. The results of this experiment can be useful for the virus classification, designing and defining the dose of vaccine for the Indian population.
Keywords: Multiple sequence alignment; Point mutation; SARS-CoV-2; SNP.
. 2020 Sep 1;104522.
doi: 10.1016/j.meegid.2020.104522. Online ahead of print.
Inferring the genetic variability in Indian SARS-CoV-2 genomes using consensus of multiple sequence alignment techniques
Indrajit Saha[SUP] 1 [/SUP], Nimisha Ghosh[SUP] 2 [/SUP], Debasree Maity[SUP] 3 [/SUP], Nikhil Sharma[SUP] 4 [/SUP], Kaushik Mitra[SUP] 5 [/SUP]
Affiliations
- PMID: 32889094
- DOI: 10.1016/j.meegid.2020.104522
Abstract
Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2) is a threat to the human population and has created a worldwide pandemic. Daily thousands of people are getting affected by the SARS-CoV-2 virus; India being no exception. In this situation, there is no doubt that vaccine is the primary prevention strategy to contain the wave of COVID-19 pandemic. In this regard, genome-wide analysis of SARS-CoV-2 is important to understand its genetical variability. This has motivated us to analyse the 566 Indian SARS-CoV-2 sequences using multiple sequence alignment techniques viz. ClustalW, MUSCLE, ClustalO and MAFFT to identify the lists of mutations as substitution, deletion, insertion and SNP. Thereafter, a consensus of these results, called as Consensus Multiple Sequence Alignment (CMSA), is considered to have the final list of mutations so that the advantages of all four alignment techniques can be preserved. The analysis shows 767, 2025 and 54 unique substitutions, deletions and SNPs in Indian SARS-CoV-2 genomes. More precisely, out of 54 SNPs, 4 SNPs are present close to the 60% of the virus population. The results of this experiment can be useful for the virus classification, designing and defining the dose of vaccine for the Indian population.
Keywords: Multiple sequence alignment; Point mutation; SARS-CoV-2; SNP.