DNA microarray

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DNA Microarray is a technology that allows scientists to examine thousands of genes simultaneously, to understand their expression levels, and to identify genetic variations. This technology has revolutionized the field of genomics, enabling large-scale studies that were previously not possible. DNA microarrays are also known as gene chips, DNA chips, or biochips.

Overview[edit | edit source]

A DNA microarray consists of a small, solid support, typically a glass slide, onto which DNA molecules are fixed in an orderly arrangement. These DNA molecules act as probes to detect complementary DNA or RNA sequences. When target sequences from a sample bind to these probes, they can be quantified, allowing for the analysis of gene expression or the identification of genetic variations.

Types of DNA Microarrays[edit | edit source]

There are two main types of DNA microarrays:

  • cDNA Microarrays: These are made by spotting cDNA onto the support. They are typically used for gene expression studies.
  • Oligonucleotide Microarrays: These contain short DNA fragments (oligonucleotides) that are synthesized directly onto the surface of the array. They can be used for both gene expression analysis and genotyping.

Applications[edit | edit source]

DNA microarray technology has a wide range of applications, including:

  • Gene Expression Profiling: Understanding the expression levels of genes in different conditions, such as healthy vs. diseased tissues.
  • Genotyping and SNP Analysis: Identifying genetic variations, such as single nucleotide polymorphisms (SNPs), which can be linked to disease susceptibility.
  • Comparative Genomic Hybridization: Comparing genomic DNA from different samples to identify genomic gains and losses.
  • Pathogen Detection: Identifying and typing pathogens by detecting their genetic material.

Procedure[edit | edit source]

The general procedure for using a DNA microarray involves:

  1. Sample Preparation: Extracting RNA or DNA from the sample.
  2. Labeling: Marking the extracted nucleic acids with fluorescent dyes.
  3. Hybridization: Incubating the labeled samples with the microarray, allowing complementary sequences to bind.
  4. Scanning: Using a laser to excite the fluorescent labels and a scanner to measure the intensity of fluorescence.
  5. Data Analysis: Analyzing the data to interpret gene expression levels or to identify genetic variations.

Challenges and Limitations[edit | edit source]

While DNA microarray technology offers many advantages, there are also challenges and limitations, including:

  • Cost: The technology can be expensive, limiting its accessibility.
  • Complexity of Data: The vast amount of data generated requires sophisticated tools and expertise for analysis.
  • Sensitivity and Specificity: There can be issues with cross-hybridization and background noise, affecting the accuracy of the results.

Future Directions[edit | edit source]

Advancements in DNA microarray technology continue to expand its applications and improve its accuracy and affordability. Integration with other technologies, such as next-generation sequencing, is opening new avenues for research and clinical diagnostics.




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Contributors: Prab R. Tumpati, MD