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A single nucleotide polymorphism or SNP is a single nucleotide variation at a specific genomic position in a large population. It is the most prevalent type of sequence variation found in the human genome. Point mutations that occur in more than 1% of the population qualify as SNPs. These are present once every 1000 nucleotides on an average in the human genome. Replacement of a purine with another purine (A/G) or a pyrimidine with another pyrimidine (C/T) is known as a transition. In contrast,...
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A Repeat Pattern of Founder Events for SARS-CoV-2 Variants in Alaska.

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Area of Science:

  • Epidemiology
  • Genomics
  • Public Health

Background:

  • Alaska's unique geography influences disease dynamics.
  • SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) variants have emerged globally.
  • Understanding variant spread in diverse populations is crucial.

Purpose of the Study:

  • To describe the pattern of SARS-CoV-2 variant emergence in Alaska.
  • To compare Alaska's variant landscape to the contiguous United States.
  • To investigate the origins and spread of specific SARS-CoV-2 Omicron sublineages in Alaska.

Main Methods:

  • Analysis of genomic surveillance data.
  • Phylogenetic analysis to infer evolutionary relationships.
  • Logistic regression modeling to assess emergence and spread patterns.

Main Results:

  • The Omicron sublineage BA.2.3 became dominant in Alaska by February 27, 2022 (48.5% of cases).
  • In contrast, BA.2.3 prevalence was lower (10.9%) in the contiguous US, where BA.1.1 dominated longer.
  • Phylogenetics suggested potential Alaskan origins for major BA.2.3 clades, with logistic regression modeling spread.

Conclusions:

  • Alaska's unique characteristics likely influenced SARS-CoV-2 variant emergence.
  • Founder events may have played a role in the spread of BA.2.3 within Alaska.
  • Genomic surveillance reveals distinct variant dynamics in geographically isolated regions.