Chromosomal Microarray Analysis – High Resolution Genome Scanning For Precise Diagnosis
Chromosomal Microarray Analysis (CMA) or simply Microarray is a whole genome genetic test available to detect a wide range of genetic syndromes, which were previously undetected by traditional technologies. Microarray scans the entire genome at a very high resolution using DNA from the individual, and provides information on thousands of genes in a single test. It can precisely define which genes are missing or extra (See box).
Traditional genetic tests such as standard chromosome studies (Karyotyping) are coarse and cannot provide precise estimate about the chromosomal regions lost or gained in an individual, and cannot exactly define the genomic content of the deletion or duplication.
The information from the microarray test provides precise information about the parts of chromosome and the genes involved in any disorder. This test is of enormous practical value to patients and physicians because it provides accurate genetic information, which can be used for improved diagnosis and treatment decisions. Microarray testing is now available for prenatal, paediatric and cancer patients. The Microarray tests are also commonly referred to as Comparative Genomic Hybridization (CGH), Array CGH or CGH Array.
Chromosomal Microarray Analysis (CMA) available through Labassure covers both Copy Number Variations (CNV) as well as Single Nucleotide Polymorphism (SNP). Labassure offers the widest options for Microarray based Genetic Testing.
Microarray tests from Labassure can be ordered from anywhere in India. Our sales team can assist you with regards to the logistics.