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Related Concept Videos

Viral Recombination00:57

Viral Recombination

Cells are sometimes infected by more than one virus at once. When two viruses disassemble to expose their genomes for replication in the same cell, similar regions of their genomes can pair together and exchange sequences in a process called recombination. Alternatively, viruses with segmented genomes can swap segments in a process called reassortment.
Conservative Site-specific Recombination and Phase Variation02:53

Conservative Site-specific Recombination and Phase Variation

Because the DNA segments are cut and reorganized in a direction-specific manner, site-specific recombination has emerged as an efficient genetic engineering technique. Flippase and Cyclization recombinases or Flp and Cre, respectively, are two members of the tyrosine recombinase family derived from bacteriophages, that are used to mediate site-specific DNA insertions, deletions, and targeted expression of proteins in mammalian cell lines.
The recognition sites for Cre recombinase called LoxP...
Mutation, Gene Flow, and Genetic Drift01:09

Mutation, Gene Flow, and Genetic Drift

In a population that is not at Hardy-Weinberg equilibrium, the frequency of alleles changes over time. Therefore, any deviations from the five conditions of Hardy-Weinberg equilibrium can alter the genetic variation of a given population. Conditions that change the genetic variability of a population include mutations, natural selection, non-random mating, gene flow, and genetic drift (small population size).
Viral Mutations00:36

Viral Mutations

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 for adaptive...
Genetic Variation01:25

Genetic Variation

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, which...
Lytic Cycle of Bacteriophages01:30

Lytic Cycle of Bacteriophages

Bacteriophages, also known as phages, are specialized viruses that infect bacteria. A key characteristic of phages is their distinctive “head-tail” morphology. A phage begins the infection process (i.e., lytic cycle) by attaching to the outside of a bacterial cell. Attachment is accomplished via proteins in the phage tail that bind to specific receptor proteins on the outer surface of the bacterium. The tail injects the phage’s DNA genome into the bacterial cytoplasm. In the lytic replication...

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Related Experiment Video

Updated: May 7, 2026

Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
09:40

Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins

Published on: June 11, 2015

V-Phaser 2: variant inference for viral populations.

Xiao Yang1, Patrick Charlebois, Alex Macalalad

  • 1Broad Institute of MIT & Harvard, 7 Cambridge Center, Cambridge, MA 02142 USA. xiaoyang@broadinstitute.org.

BMC Genomics
|October 4, 2013
PubMed
Summary

V-Phaser 2 accurately identifies low-frequency viral variants from deep sequencing data, overcoming challenges in distinguishing true variants from errors. This new software tool enhances viral population studies by improving sensitivity and specificity.

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Phage Phenomics: Physiological Approaches to Characterize Novel Viral Proteins
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Following the Dynamics of Structural Variants in Experimentally Evolved Populations

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Area of Science:

  • Virology
  • Bioinformatics
  • Genomics

Background:

  • Massively parallel sequencing enables ultra-deep coverage of viral genomes.
  • Distinguishing true low-frequency variants from sequencing errors is a significant challenge.

Purpose of the Study:

  • To develop and validate V-Phaser 2, a software package for inferring intrahost viral diversity.
  • To improve the accuracy and efficiency of analyzing ultra-deep sequencing data for viral populations.

Main Methods:

  • V-Phaser 2 utilizes paired-end read data for phased variant calling.
  • It incorporates novel strategies for representing and inferring length polymorphisms.
  • An integrated filter addresses systematic sequencing artifacts to reduce erroneous calls.

Main Results:

  • V-Phaser 2 accurately infers low-frequency intrahost variants from ultra-deep sequencing data.
  • The software demonstrated superior sensitivity and specificity compared to existing tools (QuRe, V-Phaser).
  • V-Phaser 2 achieved this performance with significantly reduced computational time and memory usage.

Conclusions:

  • V-Phaser 2 is a publicly available software tool for analyzing ultra-deep sequencing data of viral populations.
  • It efficiently processes data from common next-generation sequencing platforms.
  • The tool facilitates accurate inference of viral intrahost diversity.