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

Hardy-Weinberg Principle01:49

Hardy-Weinberg Principle

Diploid organisms have two alleles of each gene, one from each parent, in their somatic cells. Therefore, each individual contributes two alleles to the gene pool of the population. The gene pool of a population is the sum of every allele of all genes within that population and has some degree of variation. Genetic variation is typically expressed as a relative frequency, which is the percentage of the total population that has a given allele, genotype or phenotype.
Frequency-dependent Selection01:21

Frequency-dependent Selection

When the fitness of a trait is influenced by how common it is (i.e., its frequency) relative to different traits within a population, this is referred to as frequency-dependent selection. Frequency-dependent selection may occur between species or within a single species. This type of selection can either be positive—with more common phenotypes having higher fitness—or negative, with rarer phenotypes conferring increased fitness.
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).
Introduction To Survival Analysis01:18

Introduction To Survival Analysis

Survival analysis is a statistical method used to study time-to-event data, where the "event" might represent outcomes like death, disease relapse, system failure, or recovery. A unique feature of survival data is censoring, which occurs when the event of interest has not been observed for some individuals during the study period. This requires specialized techniques to handle incomplete data effectively.
The primary goal of survival analysis is to estimate survival time—the time until a...
Gene Evolution - Fast or Slow?02:05

Gene Evolution - Fast or Slow?

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...
Genetic Drift03:33

Genetic Drift

Natural selection—probably the most well-known evolutionary mechanism—increases the prevalence of traits that enhance survival and reproduction. However, evolution does not merely propagate favorable traits, nor does it always benefit populations.

You might also read

Related Articles

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

Sort by
Same author

Assessing Ancient DNA Sampling Strategies for Natural Selection Inference in Humans Using Allele Frequency Time Series Data.

Genome biology and evolution·2026
Same author

A 5500-year-old <i>Treponema pallidum</i> genome from Sabana de Bogotá, Colombia.

Science (New York, N.Y.)·2026
Same author

Out-of-Anatolia: Cultural and genetic interactions during the Neolithic expansion in the Aegean.

Science (New York, N.Y.)·2025
Same author

Pre-processing of paleogenomes: mitigating reference bias and postmortem damage in ancient genome data.

Genome biology·2025
Same author

Advances in Estimating Level-1 Phylogenetic Networks from Unrooted SNPs.

Journal of computational biology : a journal of computational molecular cell biology·2024
Same author

Towards predicting the geographical origin of ancient samples with metagenomic data.

Scientific reports·2024

Related Experiment Video

Updated: May 20, 2026

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

Estimating allele age and selection coefficient from time-serial data.

Anna-Sapfo Malaspinas1, Orestis Malaspinas, Steven N Evans

  • 1Centre for Geogenetics, Natural History Museum of Denmark, University of Copenhagen, 1350 Copenhagen, Denmark. anna.sapfo.malaspinas@snm.ku.dk

Genetics
|August 2, 2012
PubMed
Summary
This summary is machine-generated.

This study introduces a new method to estimate allele age and selection strength using time-series genetic data. The approach accurately dates genetic variations, distinguishing between new mutations and standing variation, as shown in horse coat color evolution.

More Related Videos

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
10:17

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

Published on: November 3, 2010

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data
10:46

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data

Published on: December 9, 2015

Related Experiment Videos

Last Updated: May 20, 2026

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

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations
10:17

An Allele-specific Gene Expression Assay to Test the Functional Basis of Genetic Associations

Published on: November 3, 2010

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data
10:46

A Method of Trigonometric Modelling of Seasonal Variation Demonstrated with Multiple Sclerosis Relapse Data

Published on: December 9, 2015

Area of Science:

  • Population Genetics
  • Ancient Genomics
  • Evolutionary Biology

Background:

  • Advances in sequencing yield vast ancient genomic data, enabling time-series analysis of allele frequencies.
  • Time-series data are crucial for precise inference of population genetic parameters and testing natural selection hypotheses.
  • Distinguishing selection on new mutations versus standing variation remains a key challenge in evolutionary studies.

Purpose of the Study:

  • To develop a likelihood-based method for jointly estimating selection coefficient and allele age from time-series data.
  • To provide a robust tool for analyzing allele frequency changes over time in population genetics.
  • To differentiate between selection acting on new mutations versus standing genetic variation.

Main Methods:

  • Developed a likelihood method to jointly estimate selection coefficient and allele age from time-series allele frequency data.
  • Utilized a one-step process approximation of the Wright-Fisher model's diffusion equation for transition probabilities.
  • Validated the method's accuracy and unbiasedness through extensive simulations.

Main Results:

  • The developed method provides unbiased estimates for selection coefficient and allele age.
  • Simulations confirmed the accuracy and reliability of the estimation method.
  • Application to horse coat color loci revealed an allele age predating domestication, illustrating the method's utility.

Conclusions:

  • The new method effectively estimates allele age and selection strength from time-series genomic data.
  • This approach aids in distinguishing selection on new mutations versus standing variation.
  • The findings in horse coat color suggest ancient origins for some selectively important alleles.