Genomic DNA sequence of every individual is different from others (except twins). In every new individual, a DNA mixture, half of which is inherited from the father and the other half is inherited from the mother, appears. This magnificent structure (DNA), inherited from both mother and father, carries all the necessary information to be able to live as a humanbeing.

Exclusively, relatives carry most identical DNA sequences. (i.e. mother, father and children)

The testing detects the probability of the biological paternity with an accuracy of 99.99%.

Application Reasons for Paternity Testing

· Suspected fatherhood

· Suspected motherhood

· Determining the relationship between candidate relatives

What is the testing process like?

Peripheral venous blood is preferred for the test. Our professional technical team will primarily obtain the DNA from white blood cells. Afterwards, specific regions, which are used in identity designation, are amplified, sequenced and compared by using the Nobel Prize Winner technique PCR.

Can we learn our other genetic diseases according to the results of paternity testing?

No, with paternity testing we can just determine the biological father or/and mother of the child. Absolutely, other diseases are not studied.

Caution: Before deciding for application to our lab for paternity testing, please consider if you are ready for the results of this test since there may happen 2 opposite results (biological father or not).