Introduction to Array CGH | |
Array CGH |
Introduction Array CGH (Comparative Genome Hybridization) is a high resolution technique, and it can detect chromosomal copy number changes on a genome wide. Utilizing the human cancer of CGH technological analysis, obtain several chromosome areas which easy to induce cancer from it, the scientists want to understand the carcinogenic and restraining the cancer gene in these regions and further analyze in these areas. Array CGH analyze the different chromosome of cancerous organization and to compare with the genetic mutation. To detect the specific gene of genome that has copy number changeability. At the end of genetic mutation, it could be compare to each other in gene expression, especially entire comprehensively for the 23 pairs of chromosome, and to explore the genetic transcription activity in the chromosome level. Diagnostic tool as the hereditary disease, for understand the cancer take place and how to treat has the highly help. The method is to use the different dye to label the two different cells genomic DNA, at the same time, it hybridizes with the normal chromosome, then contrast with the fluorescent intensity radio. Motivation To construct a useful and extensive website and let the users could ease to understand the array CGH. Through this website, the dream of it that is to encourage the user’s inspiration to improve problems of array CGH by inherent knowledge combined action. |
History | |
Compare | |
|
|
Example | |
Reference website | |
Reference theses | |
Message | |
![]() |
Background DNA copy number ![]() CGH
Since 1992, the CGH method for detected copy
number is widely used. A classical CGH could detect alterations affected
relatively large chromosomal regions and it has average resolution of
10-20 megabases. Hence, the array-based platforms used to filter the
copy number changes; the BAC and OaCGH arrays are mainly two
technologies, and introduced in “History”
site. |