Array CGH is proving to be a valuable tool for the detection of chromosomal imbalances in those with congenital anomalies
This microarray based service involves genome wide scanning for gains and losses of chromosomal material. This method has significantly high resolution and clinical yield, which overcomes the limitation of traditional karyotyping as even high resolution karytoypes are unreliable for detection of many known microdeletion syndromes which range from 3-5 Mb in size.
Human Genome CGH Microarray on Agilent is a high resolution tool for genome wide profiling of DNA Copy number changes associated with Cancer and other genetic diseases without amplifications or complexity reduction.
Choose from Human, Mouse, Rats, Bovine, Canine, Chicken, Chimpanzee, Rhesus Macaque and Rice Genome CGH Arrays.
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