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Related Concept Videos

FISH - Fluorescent In-situ Hybridization02:07

FISH - Fluorescent In-situ Hybridization

Fluorescence in situ hybridization, or FISH, was developed in the early 1980s and has quickly become one of the most widely used techniques in cytogenetics. Labeled probes are used to bind complementary DNA or RNA sequences on a chromosome or in a region within a cell. Earlier, the probes could only be obtained by cloning or reverse transcription of a DNA template. Currently, the probe oligonucleotides can be synthesized synthetically. Additionally, with the advancement of optical techniques,...
In-situ Hybridization02:31

In-situ Hybridization

In situ hybridization (ISH) is a technique used to detect and localize specific DNA or RNA molecules in cells, tissue, or tissue sections using a labeled probe. The technique was first used in 1969 for the investigation of nucleic acids. It is currently an essential tool in scientific research and clinical settings, especially for diagnostic purposes.
Types of probes and labels
A probe is a complementary strand of DNA or RNA that binds to corresponding nucleotide sequences in a cell. Many...
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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...
DNA Microarrays02:34

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Related Experiment Video

Updated: Jun 4, 2026

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization
16:37

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization

Published on: August 5, 2008

Comparative genomic hybridization.

J C Presti1

  • 1Department of Urology, Stanford University School of Medicine, Stanford, CA.

Methods in Molecular Medicine
|February 15, 2011
PubMed
Summary

Comparative genomic hybridization (CGH) offers a genome-wide analysis of tumor DNA copy number. This technique uses differentially labeled DNA from tumor and normal cells hybridized to metaphase spreads to detect genetic imbalances.

Area of Science:

  • Genomics
  • Molecular Biology
  • Cancer Research

Background:

  • Genetic imbalances, such as copy number variations, are hallmarks of cancer.
  • Accurate detection of these alterations is crucial for diagnosis and understanding tumor development.

Purpose of the Study:

  • To describe the principle and application of Comparative Genomic Hybridization (CGH).
  • To highlight CGH's utility in surveying genome-wide copy number alterations in tumor DNA.

Main Methods:

  • Hybridizing differentially labeled tumor DNA (Test DNA) and normal DNA (Reference DNA) to normal metaphase chromosomes.
  • Utilizing distinct fluorochrome conjugates for labeling Test and Reference DNA.
  • Analyzing the ratio of fluorescence signals to determine relative DNA copy number across the genome.

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Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
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Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

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An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants
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An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants

Published on: November 8, 2017

Related Experiment Videos

Last Updated: Jun 4, 2026

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization
16:37

Technical Demonstration of Whole Genome Array Comparative Genomic Hybridization

Published on: August 5, 2008

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
09:16

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants

Published on: February 21, 2015

An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants
09:32

An Array-based Comparative Genomic Hybridization Platform for Efficient Detection of Copy Number Variations in Fast Neutron-induced Medicago truncatula Mutants

Published on: November 8, 2017

Main Results:

  • CGH enables a comprehensive, genome-wide assessment of DNA copy number changes.
  • The method allows for the detection of both amplifications and deletions in tumor cells.
  • Genetic imbalances in abnormal cells can be visualized and quantified.

Conclusions:

  • Comparative Genomic Hybridization is a powerful tool for genome-wide copy number analysis.
  • CGH facilitates the identification of genetic aberrations in cancer.
  • This technique aids in the characterization of tumor genomes.