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Related Concept Videos

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%...
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DNA Microarrays

Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...

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Related Experiment Video

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Detection of Copy Number Alterations Using Single Cell Sequencing
09:45

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Published on: February 17, 2017

Analyzing origin activation patterns by copy number change experiments.

Miruthubashini Raveendranathan1, Anja-Katrin Bielinsky

  • 1Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota, Minneapolis, MN, USA.

Methods in Molecular Biology (Clifton, N.J.)
|July 1, 2009
PubMed
Summary
This summary is machine-generated.

This study developed a novel microarray to map DNA replication origins in yeast, revealing genome-wide activation patterns and the role of S phase checkpoints in regulating replication under stress.

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Area of Science:

  • Molecular Biology
  • Genetics
  • Cell Biology

Background:

  • Microarray technology advances DNA replication studies.
  • Genome-wide identification of replication origins in Saccharomyces cerevisiae is crucial for understanding replication dynamics.

Purpose of the Study:

  • To develop and validate a replication origin array for genome-wide analysis of DNA replication dynamics.
  • To investigate the role of S phase checkpoint kinases in regulating replication origin activation under replication stress.

Main Methods:

  • Developed a custom microarray containing approximately 430 potential yeast replication origins.
  • Arrested yeast cells in G1 and S phases.
  • Isolated and fluorescently labeled genomic DNA, then cohybridized to replication origin arrays to detect copy number changes.

Main Results:

  • Successfully generated genome-wide replication origin activation patterns in wild-type yeast, comparable to previous whole-genome array studies.
  • Applied the method to S phase checkpoint mutants, yielding insights into checkpoint kinase regulation of origin activation during replication stress.

Conclusions:

  • The developed replication origin array is a powerful tool for analyzing genome-wide replication dynamics.
  • This approach provides valuable insights into the regulation of DNA replication origin activation by S phase checkpoints under stress conditions.