Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Viral Mutations00:36

Viral Mutations

32.7K
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...
32.7K
Improving Translational Accuracy02:07

Improving Translational Accuracy

11.8K
Base complementarity between the three base pairs of mRNA codon and the tRNA anticodon is not a failsafe mechanism. Inaccuracies can range from a single mismatch to no correct base pairing at all. The free energy difference between the correct and nearly correct base pairs can be as small as 3 kcal/ mol. With complementarity being the only proofreading step, the estimated error frequency would be one wrong amino acid in every 100 amino acids incorporated. However, error frequencies observed in...
11.8K
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

7.3K
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...
7.3K
Mutation, Gene Flow, and Genetic Drift01:09

Mutation, Gene Flow, and Genetic Drift

59.1K
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).
59.1K
Point and Frameshift Mutations01:30

Point and Frameshift Mutations

56
Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...
56
Prediction Intervals01:03

Prediction Intervals

2.3K
The interval estimate of any variable is known as the prediction interval. It helps decide if a point estimate is dependable.
However, the point estimate is most likely not the exact value of the population parameter, but close to it. After calculating point estimates, we construct interval estimates, called confidence intervals or prediction intervals. This prediction interval comprises a range of values unlike the point estimate and is a better predictor of the observed sample value, y. 
2.3K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Distinctive hydrocephalus-like phenotype in NOTCH2NLC-related neuronal intranuclear inclusion disease: clinicopathological features and therapeutic implications.

Acta neuropathologica communications·2026
Same author

Decoding Early Neurochemical Dynamics in Circuit Dysfunction of Parkinson's Disease <i>via</i> Synergetic SERS and Electrophysiological Probe Suite.

Analytical chemistry·2026
Same author

Case Report: Severe protein S deficiency unmasks a cryptic <i>PROC</i> mutation with normal activity, triggering life-threatening pulmonary thromboembolism.

Frontiers in cardiovascular medicine·2026
Same author

[Evaluation of the therapeutic efficacy of retrograde diaphyseal Kirschner wire intramedullary fixation for pediatric distal radius metaphyseal-diaphyseal junction fractures].

Zhongguo gu shang = China journal of orthopaedics and traumatology·2026
Same author

High-field multi-cycle terahertz emission from axially cut β-BBO crystals reaching several hundred kV/cm.

Optics letters·2026
Same author

From nanotags to precision biomedicine: SERS-driven progress and innovation in tumor biomarker profiling, dynamic bioimaging, AI-enhanced diagnostics and therapy.

Theranostics·2026

Related Experiment Video

Updated: Aug 16, 2025

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
10:34

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells

Published on: December 9, 2022

4.4K

TEMPO: A transformer-based mutation prediction framework for SARS-CoV-2 evolution.

Binbin Zhou1, Hang Zhou2, Xue Zhang3

  • 1Department of Computer Science and Computing, Zhejiang University City College, No. 48 Huzhou Street, Hangzhou, 310015, China; Industry Brain Institute, Zhejiang University City College, Hangzhou, 310015, China.

Computers in Biology and Medicine
|December 19, 2022
PubMed
Summary
This summary is machine-generated.

Predicting SARS-CoV-2 mutations is crucial as variants challenge vaccines. TEMPO, a novel phylogenetic and transformer-based model, accurately forecasts viral evolution and outperforms existing methods.

Keywords:
Mutation predictionNatural language processingPhylogenetic treeSARS-CoV-2Transformer-based methodViral evolution

More Related Videos

Following the Dynamics of Structural Variants in Experimentally Evolved Populations
04:52

Following the Dynamics of Structural Variants in Experimentally Evolved Populations

Published on: February 3, 2023

1.0K
Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
08:46

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms

Published on: December 9, 2015

10.7K

Related Experiment Videos

Last Updated: Aug 16, 2025

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells
10:34

Probing RNA Structure with Dimethyl Sulfate Mutational Profiling with Sequencing In Vitro and in Cells

Published on: December 9, 2022

4.4K
Following the Dynamics of Structural Variants in Experimentally Evolved Populations
04:52

Following the Dynamics of Structural Variants in Experimentally Evolved Populations

Published on: February 3, 2023

1.0K
Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
08:46

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms

Published on: December 9, 2015

10.7K

Area of Science:

  • Virology
  • Computational Biology
  • Genomics

Background:

  • The continuous mutation of SARS-CoV-2 poses a significant threat to public health and economic stability.
  • Vaccine efficacy is challenged by viral evolution, necessitating accurate mutation prediction.
  • Previous studies often overlook the importance of phylogenetics in mutation prediction.

Purpose of the Study:

  • To propose and validate TEMPO, a novel model for predicting SARS-CoV-2 evolution and mutations.
  • To incorporate phylogenetic insights into a machine learning framework for enhanced prediction accuracy.
  • To assess the generalizability and robustness of TEMPO across different infectious viruses.

Main Methods:

  • Development of a phylogenetic tree-based sampling method for generating sequence evolution data.
  • Implementation of a transformer-based model to learn high-level representations of viral sequence data.
  • Leveraging a large-scale SARS-CoV-2 dataset for model training and validation.

Main Results:

  • TEMPO demonstrates high effectiveness in predicting SARS-CoV-2 mutations.
  • The proposed model significantly outperforms several state-of-the-art baseline methods.
  • Experiments on other infectious viruses confirm TEMPO's feasibility and robustness.

Conclusions:

  • TEMPO offers a powerful and effective approach for predicting viral mutations, particularly for SARS-CoV-2.
  • The integration of phylogenetics enhances the accuracy and reliability of mutation prediction models.
  • TEMPO shows promise for broader applications in tracking and predicting the evolution of infectious diseases.