You may need genetic testing either to help in your diagnosis, to predict your response to certain medications or for a screening of healthy family members to see if they have an affected gene.
This program utilises molecular genetics techniques to improve the diagnosis and risk classification of cancers. Major areas within the program include molecular detection of residual disease following chemotherapy and the use of functional genomics and high-throughput screening strategies to detect novel molecular targets and relevant inhibitors.
Molecular genetic tests (or gene tests) study single genes or short lengths of DNA to identify variations or mutations that lead to a genetic disorder.
Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder. More than 1,000 genetic tests are currently in use, and more are being developed.
Chromosomal genetic tests analyse whole chromosomes or long lengths of DNA to see if there are large genetic changes, such as an extra copy of a chromosome, that cause a genetic condition.
Biochemical genetic tests study the amount or activity level of proteins; abnormalities in either can indicate changes to the DNA that result in a genetic disorder.