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Related Concept Videos

Genetic Screens02:46

Genetic Screens

Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
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Evolutionary Relationships through Genome Comparisons02:54

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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...
Next-generation Sequencing03:00

Next-generation Sequencing

The first human genome sequencing project cost $2.7 billion and was declared complete in 2003, after 15 years of international cooperation and collaboration between several research teams and funding agencies. Today, with the advent of next-generation sequencing technologies, the cost and time of sequencing a human genome have dropped over 100 fold.
Next-Generation Sequencing Methods
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Genome-wide Association Studies-GWAS01:11

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Genome-wide association studies or GWAS are used to identify whether common SNPs are associated with certain diseases. Suppose specific SNPs are more frequently observed in individuals with a particular disease than those without the disease. In that case, those SNPs are said to be associated with the disease. Chi-square analysis is performed to check the probability of the allele likely to be associated with the disease.
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Pharmacogenomics: Identification of New Drug Targets01:29

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Advances in genomics have profoundly influenced drug discovery by increasing both the speed and accuracy of pharmaceutical development. Pharmacogenomics, which examines how genetic variation influences drug response, facilitates the identification of novel therapeutic targets and enables patient stratification for personalized treatment. These strategies contribute to improved drug efficacy, minimized adverse effects, and more efficient clinical trial design.Mapping genetic differences...

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Related Experiment Video

Updated: Jun 19, 2026

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay (EMSA) and DNA-affinity Precipitation Assay (DAPA)
11:35

Screening for Functional Non-coding Genetic Variants Using Electrophoretic Mobility Shift Assay (EMSA) and DNA-affinity Precipitation Assay (DAPA)

Published on: August 21, 2016

[Advances in detecting positive selection on genome].

Kao Lin1, Hai-Peng Li

  • 1CAS-MPG Partner Institute for Computational Biology, Chinese Academy of Sciences, Shanghai, China. linkao@picb.ac.cn

Yi Chuan = Hereditas
|October 13, 2009
PubMed
Summary

Researchers review methods for detecting natural selection in populations. They discuss how DNA data helps identify adaptive evolutionary history, while acknowledging challenges from population demographics and other evolutionary forces.

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Area of Science:

  • Evolutionary biology
  • Population genetics
  • Molecular evolution

Context:

  • Darwin's theory of natural selection and Kimura's neutral theory of molecular evolution provide frameworks for understanding evolutionary forces.
  • Advancements in DNA sequencing have generated extensive polymorphism data, enabling empirical testing of evolutionary theories.
  • Distinguishing the genomic footprints of natural selection from population demographic history and other evolutionary forces is a key challenge.

Purpose:

  • To summarize fundamental concepts of neutral tests in evolutionary biology.
  • To provide an overview of classical methods used to detect natural selection.
  • To highlight and discuss recently developed methodologies for analyzing genomic data.

Summary:

  • This paper reviews the theoretical underpinnings and practical applications of neutral tests for inferring natural selection.
  • It examines how DNA sequence polymorphism data can reveal adaptive evolutionary trajectories.
  • The review addresses the complexities introduced by population demographic factors and other evolutionary processes that can mimic selection signals.

Impact:

  • Provides a consolidated resource for researchers studying evolutionary processes using genomic data.
  • Facilitates a deeper understanding of the interplay between natural selection, neutral evolution, and population dynamics.
  • Aims to improve the accuracy and reliability of detecting natural selection in diverse populations.