What is Amplification in the Context of Neonatal Disorders?
Amplification refers to the process of increasing the number of copies of a specific DNA sequence. This is crucial for genetic testing in neonates, as it allows for the detection of even minute quantities of DNA, which may be present in limited amounts in samples collected from newborns. Techniques such as Polymerase Chain Reaction (PCR) are commonly used to amplify DNA sequences, making it easier to identify genetic mutations or anomalies that could be indicative of neonatal disorders.
