Related Experiment Video
Updated: Jun 4, 2026

Array Comparative Genomic Hybridization (Array CGH) for Detection of Genomic Copy Number Variants
Published on: February 21, 2015
Microarray-based CGH and copy number analysis of FFPE samples.
1Molecular Pathology Unit, Health Sciences Center, Safat, Kuwait. fahd@al-mulla.org
Array-based Comparative Genomic Hybridization (aCGH) offers high-resolution detection of genome-wide copy number alterations. This guide details optimal handling of DNA from formalin-fixed paraffin-embedded tissues for superior aCGH data acquisition.
Area of Science:
- Biomedical research
- Genomics
- Cancer research
Background:
- Microarray technology has become a vital tool in biomedical research, particularly for understanding complex diseases like cancer.
- Array-based Comparative Genomic Hybridization (aCGH) enables high-resolution, genome-wide detection of copy number alterations.
- Utilizing DNA from formalin-fixed paraffin-embedded (FFPE) tissues for microarray analysis presents challenges due to DNA degradation.
Purpose of the Study:
- To describe available CGH-microarray platforms.
- To provide practical guidance for optimal handling of FFPE-extracted DNA.
- To ensure superior aCGH data acquisition from FFPE samples.
Main Methods:
- Description of various CGH-microarray platforms.
- Detailed protocols for DNA extraction and handling from FFPE tissues.
- Methodologies for high-quality aCGH data acquisition.
Main Results:
- Successful implementation of aCGH on FFPE-derived DNA is feasible with optimized protocols.
- High-resolution detection of copy number alterations is achievable.
- Practical steps enhance data quality and reliability.
Conclusions:
- Optimized protocols enable effective use of FFPE tissues for aCGH analysis.
- Microarray technology, including aCGH, provides valuable insights into cancer genomics.
- This work facilitates advanced molecular studies using archival FFPE samples.
More Related Videos
13:24Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016
09:32An 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 Concept Videos
DNA Microarrays
Comparing Copy Number Variations and SNPs
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%...