Agilent Oligonucleotide Array-Based CGH Brochure

This white paper introduces Agilent Oligonucleotide Array-Based Comparative Genomic Hybridization (CGH) technology, a highly sensitive technology for analyzing genomic and chromosomal abnormalities. The technology is based on the Agilent DNA Microarray platform, which can analyze copy number changes of genomic DNA to perform chromosome analysis.


Agilent Oligonucleotide Array-Based CGH Brochure - cover page
Brand
Agilent
Category
Other
Document type
Product Leaflet
Language
English
Pages
8
File format
PDF
File size
468 KB
Published
03 July, 2012
Updated
30 September, 2023
MD5 checksum
E81F4AF4128C8A1B479000B0C93B1A69

About this manual

The document introduces the Agilent DNA Microarray Platform, which utilizes oligonucleotide microarrays to revolutionize comparative genomic hybridization (CGH). It addresses limitations of traditional methods and BAC/cDNA arrays by offering higher resolution, flexibility, and sensitivity for detecting chromosomal variations.

What's inside

  • Oligonucleotide Array-Based CGH
  • SurePrint Inkjet Technology
  • 60-mer Oligonucleotide Probes
  • CGH Analytics Software
  • Sample Preparation
  • Hybridization and Scanning
  • High-Definition Analysis
  • Multiplexed Arrays
  • eArray Design Tool
  • GeneSpring Software Platform

Frequently asked questions

What sample types are compatible with the Agilent Oligo aCGH arrays?

The arrays are compatible with tissues, cell lines, whole blood, and other challenging samples.

What is the overall median probe spacing for HD-CGH arrays?

The overall median probe spacing is 8.9 kb.

How much labeled DNA was used in the experimental conditions described?

The experiment used 1.5 yg of labeled DNA.

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