Mutation Frequency Calculation

Mutation frequency calculation is a quantitative method for determining how often a specific genetic change occurs within a sampled population, making it useful for tracking variation in pathogens and immune-related cell populations. It typically involves identifying mutant sequences or cells, dividing their count by the total number analyzed, and expressing the result as a proportion or percentage, while accounting for sampling and detection limits. In immunology and infection research, these measurements help monitor viral or bacterial evolution, antigenic variation, immune escape, and the emergence of drug resistance. Comparing frequencies across time points or conditions can reveal selection pressures and inform disease surveillance and treatment strategies.

Mutation Frequency Calculation - Related Videos

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JoVE EoE - Bacterial Growth and Techniques

Evaluating Mutation Frequency in Bacteria Using the Beta-Glucosidase Assay

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2025

Source: Stefan, A., et al. The Multifaceted Benefits of Protein Co-expression in Escherichia coli. J. Vis. Exp. (96), (2015).This video demonstrates the evaluation of mutation frequency in bacteria using a beta-glucosidase assay. Bacterial cultures expressing a proofreading-deficient DNA polymerase are collected over successive generations. Replication errors caused by reduced proofreading may activate a suppressed beta-glucosidase gene. After centrifugation and permeabilization, a substrate is...

Research

JoVE Journal - Immunology and Infection
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Isolation of Fidelity Variants of RNA Viruses and Characterization of Virus Mutation Frequency

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Cited by 40 •

2011

The present article describes the steps required to isolate and characterize RNA polymerase fidelity variants of RNA viruses and how to use mutation frequency data to confirm fidelity changes in tissue culture.

Wild-Type Blocking PCR to Detect Low-Frequency Somatic Mutations

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2025

This video describes wild-type blocking polymerase chain reaction, or WTB-PCR, which detects somatic mutations. The PCR-based technique uses a locked nucleic acid, or LNA, an oligonucleotide that binds to its complementary wild-type allele and blocks its elongation. The blocking selectively allows the amplification of low-level mutant alleles over their wild-type variants in the sample.

Wild-type Blocking PCR Combined with Direct Sequencing as a Highly Sensitive Method for Detection of Low-Frequency Somatic Mutations

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Cited by 5 •

2017

Wild-type blocking PCR followed by direct sequencing offers a highly sensitive method of detection for low frequency somatic mutations in a variety of sample types.

Quantification of Colonic Stem Cell Mutations

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Cited by 1 •

2015

We report significant improvements for the reproducible measurement of somatic colonic stem cell mutations after exposure of mice to potential DNA damaging agents.

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