9. High-Throughput Multiplex HLA-Typing by Ligase Detection Reaction (LDR) and Universal Array (UA) Approach
| Abstract |
|
|
One major goal of genetic research is to understand the role of genetic variation in living systems. In humans, by far the
most common type of such variation involves differences in single DNA nucleotides, and is thus termed single nucleotide polymorphism
(SNP). The need for improvement in throughput and reliability of traditional techniques makes it necessary to develop new
technologies. Thus the past few years have witnessed an extraordinary surge of interest in DNA microarray technology. This
new technology offers the first great hope for providing a systematic way to explore the genome. It permits a very rapid analysis
of thousands genes for the purpose of gene discovery, sequencing, mapping, expression, and polymorphism detection. We generated
a series of analytical tools to address the manufacturing, detection and data analysis components of a microarray experiment.
In particular, we set up a universal array approach in combination with a PCR-LDR (polymerase chain reaction-ligation detection
reaction) strategy for allele identification in the HLA gene.
Series: Methods in Molecular Biology | Volume: 496 | Pub. Date: Oct-24-2008 | Page Range: 115-127 | DOI: 10.1007/978-1-59745-553-4_9
Subject: Genetics/Genomics
Key Words: Chitosan - amino-modified oligonucleotides - ligation detection reaction - universal array - human leukocyte antigen - single nucleotide polymorphisms
Comments (Loading...) |
||
Loading... |





















