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Related Concept Videos

Evolutionary Relationships through Genome Comparisons02:54

Evolutionary Relationships through Genome Comparisons

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...
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...
What is Population Genetics?01:25

What is Population Genetics?

A population is composed of members of the same species that simultaneously live and interact in the same area. When individuals in a population breed, they pass down their genes to their offspring. Many of these genes are polymorphic, meaning that they occur in multiple variants. Such variations of a gene are referred to as alleles. The collective set of all the alleles within a population is known as the gene pool.While some alleles of a given gene might be observed commonly, other variants...
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...
Comparing Copy Number Variations and SNPs02:26

Comparing Copy Number Variations and SNPs

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%...
Genome Size and the Evolution of New Genes03:21

Genome Size and the Evolution of New Genes

While every living organism has a genome of some kind (be it RNA, or DNA), there is considerable variation in the sizes of these blueprints. One major factor that impacts genome size is whether the organism is prokaryotic or eukaryotic. In prokaryotes, the genome contains little to no non-coding sequence, such that genes are tightly clustered in groups or operons sequentially along the chromosome. Conversely, the genes in eukaryotes are punctuated by long stretches of non-coding sequence.

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Related Experiment Video

Updated: Jun 17, 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

Population genetic inference from genomic sequence variation.

John E Pool1, Ines Hellmann, Jeffrey D Jensen

  • 1Department of Integrative Biology, University of California, Berkeley, Berkeley, California 94720, USA.

Genome Research
|January 14, 2010
PubMed
Summary
This summary is machine-generated.

Population genetics is now data-driven, using whole-genome data to study population history and natural selection. Falling sequencing costs will expand these genomic analyses to more organisms.

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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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Last Updated: Jun 17, 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

Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease
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Targeted Next-generation Sequencing and Bioinformatics Pipeline to Evaluate Genetic Determinants of Constitutional Disease

Published on: April 4, 2018

Area of Science:

  • Genomics
  • Evolutionary Biology
  • Population Genetics

Background:

  • Population genetics has transitioned from a theory-focused field to a data-driven discipline.
  • Genome-scale datasets are pushing the boundaries of computational analysis and modeling.
  • Whole-genome sequence polymorphism data is increasingly available for humans and model organisms.

Purpose of the Study:

  • To assess the challenges associated with analyzing whole-genome sequence polymorphism data.
  • To explore the potential of these data for new insights into population history.
  • To investigate the genomic prevalence of natural selection.

Main Methods:

  • Analysis of genome-scale datasets.
  • Computational analysis of polymorphism data.
  • Leveraging next-generation sequencing technologies.

Main Results:

  • Whole-genome sequence polymorphism data analysis presents significant computational challenges.
  • These datasets offer substantial potential for advancing our understanding of population history.
  • Genomic data can reveal the prevalence and patterns of natural selection across genomes.

Conclusions:

  • The analysis of whole-genome sequence polymorphism data is a rapidly advancing area.
  • Future studies will benefit from falling sequencing costs, enabling broader application.
  • These data promise to deepen our knowledge of evolutionary processes and genomic variation.