Fetal DNA testing is a method of analyzing the DNA of the fetus and comparing it with the alleged father. From there, there is a basis for determining the blood relationship between the participants.
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Fetal DNA testing is a method of analyzing the DNA of the fetus and comparing it with the alleged father. From there, there is a basis for determining the blood relationship between the participants. One of the great advances in medicine is the ability to do DNA testing while the baby is still in the mother’s womb.
Based on the implementation method, fetal DNA testing can be divided into 2 groups of methods, including 2 methods: Invasive and Non-invasive.
DNA TESTING PROCEDURE
The process of performing paternity DNA testing at LOCI Molecular Biology Institute includes the following steps:
Customers who want to test their bloodline DNA will contact LOCI for consultation and registration for testing. LOCI consultants will guide customers through the procedures, processes and advise them on testing services.
For NON-INVASIVE testing, 10ml of the mother’s venous blood is taken. For INVASIVE testing, an obstetrician will examine and collect the mother’s sample, and for the father’s sample, a random sample is collected.
The DNA samples collected will be sent to LOCI’s laboratory for analysis. The normal bloodline DNA analysis process will take about 06 hours – 01 day, there is a service to rush the results.
LOCI sends results directly to test registrants in the form of: at the office, post office, email, phone and receive in-depth consultation on the results from a specialist. Commitment to absolute confidentiality
DNA test results are important and LOCI is the place you can put your trust in.
PRICE LIST FOR FATHER AND CHILD DNA TESTING
Thời gian trả kết quả không bao gồm ngày thu mẫu, Thứ 7, Chủ Nhật và các ngày Lễ
Hoàn toàn không phụ thu thêm tiền phí với các loại mẫu đặc biệt (tất cả các mẫu chỉ có một mức giá duy nhất)
Được xét nghiệm lần 02 hoàn toàn miễn phí nếu kết quả không cùng huyết thống để đưa ra kết luận cuối cùng.
Trường hợp xét nghiệm ADN Pháp lý, nhân viên của Viện LOCI sẽ trực tiếp thu mẫu.
Nếu bạn có nhu cầu thu mẫu tại nhà vui lòng liên hệ hotline.
Amniotic fluid DNA testing has the advantage of being quick and cost-effective. Invasive DNA testing is generally considered safe, but like any medical procedure, it carries some risks. Some of these risks include:
– Miscarriage (very low rate, about 1/500)
– Amniotic fluid leakage
– Uterine muscle contractions or cramps
– Irritation at the puncture site or vagina
– Risk of infection
In particular, pregnant women with Rh- blood type need to be extremely careful because this blood type is rare, and has a higher risk of miscarriage or blood-related complications.
Amniocentesis requires careful preparation before performing, including an ultrasound to ensure safety. The safety rate of this method is very high (99.8%), with a risk rate of only about 0.2%.
To ensure the invasive DNA testing process is safe, pregnant women need to strictly follow the doctor’s instructions and not arbitrarily handle any unusual situations without professional knowledge.
The assumed father sample can collect samples such as blood, hair roots, fur, beard, sperm… all of which can be tested.
The invasive method of collecting amniotic fluid samples for DNA testing can be performed from the 14th week of pregnancy, when the amount of baby cells shed in the amniotic fluid will have enough DNA to perform a definitive DNA test
The non-invasive method can be performed when the fetus is 7 weeks old.
