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What is DNA Paternity Testing?

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What is DNA Paternity Testing?

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We all have a unique DNA pattern that is inherited from our biological parents and is similar to theirs in molecular structure and genetic code. Because of this similarity, the DNA can be used to test and conclusively determine biological kinship. When the testing is done to determine who the father is, it is known as DNA Paternity Testing. It is about 99.99% conclusive. It is usually not necessary to do maternity testing. DNA Paternity Testing is now widely used for scientific purposes, to determine paternity concerns, or to settle legal disputes. What does DNA Paternity Testing involve? Usually, DNA from the alleged parents and the child are required for the DNA Paternity Testing. Having access to the maternal DNA makes the testing easier, as, with this part conclusively settled, you only need to check the other half of the child’s DNA with that of the father. If the DNA sequence shows a strong similarity, then the Paternity is proved.

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Paternity means the state of being a father. Currently, DNA paternity testing, free or paid for, can determine who the father of a child is with almost 100 percent absolute certainty. In past years, DNA testing has improved so much and is so reliable that it’s considered court worthy when a judge is deciding cases related to paternity, guardianship, and monetary requirements of a birth father. How DNA testing works is a long, complicated story. Basically, each human on the planet has one unique set of DNA – this DNA set is an offset from the unique patterns of parent DNA, which is how paternity is able to be sorted out. The only time DNA is not unique is among identical twins or other identical multiples (like triplets). You can conduct paternity testing either during pregnancy or after the baby arrives. To see an in-depth DNA testing explanation, visit Understanding Genetics.

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