NON-INVASIVE PATERNITY TESTS: WHAT ARE THEY ABOUT?
Publicado el: 09/04/2025
The non-invasive prenatal paternity test is the most technologically advanced way to determine paternity during pregnancy. It involves taking a blood sample from the expecting mother and a sample from the alleged father, as fetal circulating free DNA can be obtained from the mother’s blood.
This non-invasive test is 100% safe for both the mother and the fetus, with no risk of miscarriage. To obtain the fetal sample, at least 10 ml of the mother’s peripheral blood must be collected in special tubes. Please contact us to schedule the most suitable day for the blood draw at our facilities. An appointment is required. When booking, make sure to specify that you need a Non-Invasive Prenatal Paternity Test.
For the alleged father’s sample, the following types of biological samples can be used:
- At least 2 ml of blood with EDTA anticoagulant.
- At least 5 blood spots larger than 0.3 cm² on FTA paper.
- At least 6 swabs rubbed inside the mouth. Please allow them to air dry for at least 1 hour and store them in a paper envelope rather than plastic.
In addition to paternity testing, there is also the option to determine the fetus’s sex and screen for trisomies/aneuploidies in chromosomes 21, 18, 13, X, and Y, as well as up to 93 types of microdeletion/microduplication syndromes.
Related news
SEARCH BY DISEASE OR GENE

Request information
LabGenetics offers a comprehensive, personalized, and flexible genetic diagnostic service tailored to the needs of healthcare professionals, continuously introducing new genetic diagnoses of hereditary and rare diseases into its service portfolio. Our goal is to establish close collaborations to achieve accurate and suitable results for each case as quickly and cost-effectively as possible.
Additionally, we have pioneering professionals in performing DNA paternity and maternity tests, both informational and with legal validity, as well as prenatal and postmortem tests.
We also conduct kinship tests such as grandparentage, mitochondrial DNA for maternal lineage studies, Y chromosome for paternal lineage studies, and complex kinship studies using autosomal STRs, genetic footprints, biological fluid detection, and biological criminalistics, ancestry studies, and DNA tests for individuals affected by irregular adoptions or newborn abductions.
