Paternity DNA Testing

Service Description

Paternity DNA testing, also known as a paternity test, is a type of genetic test used to determine the biological relationship between a possible father and a child. This test compares the DNA profiles of the alleged father and child to determine the probability of paternity. The process of paternity DNA testing typically involves collecting DNA samples from both the alleged father and the child. The most common method of collecting DNA samples is through a buccal swab, which is a painless process of swabbing the inside of the cheek to collect cells for analysis. These samples are then sent to a laboratory for testing. In the laboratory, the DNA samples are analyzed to identify specific genetic markers known as DNA markers or genetic loci. The paternity test compares the genetic markers between the alleged father and child to determine if they share a biological relationship. The analysis examines specific regions of the DNA that are highly polymorphic, meaning they contain variations that are unique to each individual. By comparing these genetic markers, paternity can be established with a high degree of accuracy.