Introduction to Multi Nucleotide Variants

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10.1016/j.omtn.2021.07.016

Multi-nucleotide variants (MNVs) represent an important type of genetic variation and have biological and clinical significance.

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10.1016/j.jgg.2021.01.004

High genome coverage allowed the identification of single and multi-nucleotide variants in SARS-CoV-2 in the community and their phylogenetic relationships with other variants present during the same period of the outbreak.

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10.1101/2021.05.21.445151

VCF can present single nucleotide variants, multi-nucleotide variants, insertions and deletions, and simple structural variants called against a reference genome.

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10.3389/fgene.2021.659287

These tools annotate variants independently without considering the potential effect of grouped or haplotypic variations, often called “multi-nucleotide variants” (MNVs).

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Multi Nucleotide Variants

Encyclopedia

Aug 17, 2022

What is/are Multi Nucleotide Variants?

Multi Nucleotide Variants - Multi-nucleotide variants (MNVs) represent an important type of genetic variation and have biological and clinical significance. ^[1] High genome coverage allowed the identification of single and multi-nucleotide variants in SARS-CoV-2 in the community and their phylogenetic relationships with other variants present during the same period of the outbreak. ^[2] VCF can present single nucleotide variants, multi-nucleotide variants, insertions and deletions, and simple structural variants called against a reference genome. ^[3] These tools annotate variants independently without considering the potential effect of grouped or haplotypic variations, often called “multi-nucleotide variants” (MNVs). ^[4]