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Related Concept Videos

Viral Mutations00:36

Viral Mutations

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A mutation is a change in the sequence of bases of DNA or RNA in a genome. Some mutations occur during replication of the genome due to errors made by the polymerase enzymes that replicate DNA or RNA. Unlike DNA polymerase, RNA polymerase is prone to errors because it is not capable of “proofreading” its work. Viruses with RNA-based genomes, like HIV, therefore accrue mutations faster than viruses with DNA-based genomes. Because mutation and recombination provide the raw material...
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Single Nucleotide Polymorphisms-SNPs01:05

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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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Gene Evolution - Fast or Slow?02:05

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The genomes of eukaryotes are punctuated by long stretches of sequence which do not code for proteins or RNAs. Although some of these regions do contain crucial regulatory sequences, the vast majority of this DNA serves no known function. Typically, these regions of the genome are the ones in which the fastest change, in evolutionary terms, is observed, because there is typically little to no selection pressure acting on these regions to preserve their sequences.
In contrast, regions which code...
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Genetic Variation01:25

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Genetic variation is the diversity in DNA sequences found among individuals of the same species. This diversity is crucial for a species' survival because it helps organisms adapt to environmental changes. Genetic variation begins with fertilization, where an egg and sperm cell merge. Each of these cells carries 23 chromosomes, up to 46 in the fertilized egg. Chromosomes are long DNA strands that contain genes, the basic units of heredity.
Genes exist in different versions called alleles,...
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Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

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Genome comparison is one of the excellent ways to interpret the evolutionary relationships between organisms. The basic principle of genome comparison is that if two species share a common feature, it is likely encoded by the DNA sequence conserved between both species. The advent of genome sequencing technologies in the late 20th century enabled scientists to understand the concept of conservation of domains between species and helped them to deduce evolutionary relationships across diverse...
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Comparing Copy Number Variations and SNPs02:26

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
Copy number variations or CNVs are the structural variations that cover more than 1kb of DNA sequence. The single nucleotide polymorphism (SNP), on the other hand, is a single nucleotide change or a point mutation that is found in more than 1%...
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Updated: Aug 31, 2025

Quantification and Whole Genome Characterization of SARS-CoV-2 RNA in Wastewater and Air Samples
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SARS-CoV-2 genome variations and evolution patterns in Egypt: a multi-center study.

Deena Jalal1, Mariam G Elzayat1, Hend E El-Shqanqery1

  • 1Genomics Program, Department of Basic Research, Children's Cancer Hospital Egypt 57357, Cairo, Egypt.

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|August 25, 2022
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Summary
This summary is machine-generated.

This study tracked the spread of SARS-CoV-2 variants in Egypt, identifying mutations linked to increased COVID-19 severity. Genetic analysis revealed specific viral clades and spike protein variants circulating in the region.

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Area of Science:

  • Virology
  • Genomics
  • Epidemiology

Background:

  • The COVID-19 pandemic, caused by SARS-CoV-2, emerged in late 2019.
  • Tracking viral evolution and variants is crucial for understanding transmission dynamics.

Purpose of the Study:

  • To analyze the genetic diversity and phylogenetic patterns of SARS-CoV-2 in Egypt.
  • To identify mutations associated with clinical severity of COVID-19.

Main Methods:

  • Whole-genome sequencing of 110 SARS-CoV-2 samples collected between May 2020 and January 2021.
  • Phylogenetic analysis using Nextstrain clades.
  • Correlation of genetic variants with clinical severity data.

Main Results:

  • Sequenced samples predominantly belonged to Nextstrain clades 20A and 20D, with clade 20B present early on.
  • The D614G spike protein variant showed high prevalence.
  • Four specific mutations (spike H49Y, ORF3a H78Y, ORF8 E64stop, nucleocapsid E378V) were associated with increased disease severity.

Conclusions:

  • The study provides crucial genetic and phylogenetic data on SARS-CoV-2 spread in Egypt.
  • Identified mutations offer potential biomarkers for predicting COVID-19 severity.
  • Findings contribute to understanding the pandemic's evolution in the region.