We offer three types of DNA paternity testing, one of which is ideal for your unique situation. On this page are brief overviews for Legal Paternity, Home Paternity, and Prenatal Paternity tests, along with a series of FAQs at the bottom of the page that answer popular questions.
Legal DNA paternity testing (also known as chain-of-custody testing) provides results that may be used as proof of relationship for child support, custody, immigration, birth certificate, Social Security, or other legal reasons. Although this type of accurate DNA paternity test requires on-site testing, our network of paternity-testing collection sites makes the process easier.
Legal paternity testing (also known as chain-of-custody testing) provides results that may be used as proof of relationship for child support, custody, immigration, birth certificate, Social Security, or other legal reason. Although this type of accurate paternity test requires on-site testing, our network of paternity-testing collection sites makes the process easier.
A home DNA paternity test kit is an excellent choice if you want an answer for personal knowledge or peace of mind only. Since test participants collect and submit their own DNA, results are not court-admissible. With prices starting at $199, our easy-to-use mail-in paternity test provides peace of mind right from the comfort of home.
A home paternity test kit is an excellent choice if you want an answer for personal knowledge or peace of mind only. Because test participants collect and submit their own DNA, results are not court-admissible. With prices starting at $199, our easy-to-use mail-in paternity test provides peace of mind right from the comfort of home.
A prenatal DNA paternity test provides paternity answers during pregnancy. Our technically-advanced, non-invasive test is AABB-accredited, accurate, can be performed as early as 7 weeks, and is completely safe for the mother and pregnancy.
A prenatal paternity test is for couples seeking answers while the woman is still pregnant. Our technically-advanced non-invasive test is AABB-accredited, accurate, can be performed as early as 7 weeks, and is completely safe for mother and pregnancy.
A: DDC prides itself on delivering quick and accurate results. Home-test and legal-test results are generally posted 2 business days after samples are received at our lab, although next-day and same-day results are available for an additional fee. Non-invasive prenatal paternity test results are posted 7 business days after samples are received at the lab or in 3 business days for an additional fee.
You want to determine the paternity or maternity of a child but you are not involved in a court matter, you should purchase a non-legal at-home test. If there is any chance the results might be needed for legal purposes, a legal test should be performed. Labcorp uses the same testing technology for both legal and non-legal testing. Non-legal or at-home tests allow for sample collection at your home and do not follow the legal chain-of-custody protocols needed for a legal test. Our highly accurate tests exclude, on average, 99.99% of non-fathers.
A DNA collection kit will be delivered to you. The kit will contain 4 cotton swabs for each person that will be providing their sample for testing. DNA samples can be collected at home by rubbing the cotton swab on the inside of the cheek.
DNA paternity testing is the use of DNA profiles to determine whether an individual is the biological parent of another individual. Paternity testing can be especially important when the rights and duties of the father are in issue and a child's paternity is in doubt. Tests can also determine the likelihood of someone being a biological grandparent. Though genetic testing is the most reliable standard, older methods also exist, including ABO blood group typing, analysis of various other proteins and enzymes, or using human leukocyte antigen antigens. The current techniques for paternity testing are using polymerase chain reaction (PCR) and restriction fragment length polymorphism (RFLP). Paternity testing can now also be performed while the woman is still pregnant from a blood draw.
DNA testing is currently the most advanced and accurate technology to determine parentage. In a DNA paternity test, the result (called the 'probability of parentage)[failed verification] is 0% when the alleged parent is not biologically related to the child, and the probability of parentage is typically 99.99% when the alleged parent is biologically related to the child. However, while almost all individuals have a single and distinct set of genes, rare individuals, known as "chimeras", have at least two different sets of genes, which can result in a false negative result if their reproductive tissue has a different genetic make-up from the tissue sampled for the test.
The DNA test is performed by collecting buccal (cheek) cells found on the inside of a person's cheek using a buccal or cheek swab. These swabs have wooden or plastic stick handles with a cotton on synthetic tip. The collector rubs the inside of a person's cheek to collect as many buccal cells as possible, which are then sent to a laboratory for testing. Samples from the alleged father or mother and the child would be needed.
Advances in genetic testing have led to the ability to identify the biological father while the woman is still pregnant. There is a small amount of fetal DNA (cffDNA) present in the mother's blood during pregnancy. This allows for accurate fetal DNA paternity testing during pregnancy from a blood draw with no risk of miscarriage. Studies have shown that cffDNA can first be observed as early as 7 weeks gestation, and the amount of cffDNA increases as the pregnancy progresses.
Besides nuclear DNA, mitochondria also have their own genetic material called mitochondrial DNA. Mitochondrial DNA comes only from the mother, without any shuffling. Proving a relationship based on comparison of the mitochondrial genome is much easier than that based on the nuclear genome. However, testing the mitochondrial genome can prove only if two individuals are related by common descent through maternal lines only from a common ancestor and is, thus, of limited value (i.e., it could not be used to test for paternity).
In testing the paternity of a male child, comparison of the Y chromosome can be used, since it is passed directly from father to son. However, similar to mitochondrial DNA, the Y chromosome is passed through the paternal line. Meaning two brothers share the Y chromosome of their father. Therefore if one brother is the suspected father, his biological brother could also be the father based on Y chromosomal data alone. This is true with any male related to the suspected father on the paternal line. For this reason autosomal DNA testing would be a more precise paternity testing method. 
In the US, the AABB has regulations for DNA paternity and family relationship testing, but AABB accreditation is not required. DNA test results are legally admissible if the collection and the processing follows a chain of custody. Similarly in Canada, the SCC has regulations on DNA paternity and relationship testing, but this accreditation, while recommended, is not required.
The Paternity Testing Commission of the International Society for Forensic Genetics has taken up the task of establishing the biostatistical recommendations in accordance with the ISO/IEC 17025 standards. Bio-statistical evaluations of paternity should be based on a likelihood ratio principle - yielding the Paternity Index, PI. The recommendations provide guidance on concepts of genetic hypotheses and calculation concerns needed to produce valid PIs, as well as on specific issues related to population genetics.
The first form of any kind of parental testing was blood typing, or matching blood types between the child and alleged parent, which became available in the 1920s, after scientists recognized that blood types, which had been discovered in the early 1900s, were genetically inherited. Under this form of testing, the blood types of the child and parents are compared, and it can be determined whether there is any possibility of a parental link. For example, two O blood type parents can produce a child only with an O blood type, and two parents with a B blood type can produce a child with either a B or an O blood type. This often led to inconclusive results, as 30% of the entire population can be excluded from being the possible parent under this form of testing. In the 1930s, serological testing, which tests certain proteins in the blood, became available, with a 40% exclusion rate.
In the 1960s, accurate genetic paternity testing became a possibility when HLA typing was developed, which compares the genetic fingerprints on white blood cells between the child and alleged parent. HLA tests could be done with 80% accuracy but could not distinguish between close relatives. Genetic parental testing technology advanced further with the isolation of the first restriction enzyme in 1970. Highly accurate DNA parental testing became available in the 1980s with the development of RFLP. In the 1990s, PCR became the standard method for DNA parental testing: a simpler, faster, and more accurate method of testing than RFLP, it has an exclusion rate of 99.99% or higher.
In the U.S., immigration applicants bear the responsibility of arranging and paying for DNA testing. The U.S. immigration authorities require that the DNA test, if pursued, be performed by one of the laboratories accredited by the AABB (formerly American Association of Blood Banks). Similarly, in Canada, the laboratory needs to be accredited by the Standards Council of Canada.
Although paternity tests are more common than maternity tests, there may be circumstances in which the biological mother of the child is unclear: examples include cases of an adopted child attempting to reunify with his or her biological mother, potential hospital mix-ups, and in vitro fertilization where the laboratory may have implanted an unrelated embryo inside the mother. 041b061a72