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Computational Advances in Bio and Medical Sciences ; 12686:127-141, 2021.
Article in English | Web of Science | ID: covidwho-2003651

ABSTRACT

With the availability of more than half a million SARS-CoV-2 sequences and counting, many approaches have recently appeared which aim to leverage this information towards understanding the genomic diversity and dynamics of this virus. Early approaches involved building transmission networks or phylogenetic trees, the latter for which scalability becomes more of an issue with each day, due to its high computational complexity. In this work, we propose an alternative approach based on clustering sequences to identify novel subtypes of SARS-CoV-2 using methods designed for haplotyping intra-host viral populations. We assess this approach using cluster entropy, a notion which very naturally captures the underlying process of viral mutation-the first time entropy was used in this context. Using our approach, we were able to identify the well-known B.1.1.7 subtype from the sequences of the EMBL-EBI (UK) database, and also show that the associated cluster is consistent with a measure of fitness. This demonstrates that our approach as a viable and scalable alternative to unveiling trends in the spread of SARS-CoV-2.

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