Paternity Testing - Basics (17)

What kind of testing is performed to determine paternity?

DNA testing is performed. DNA (DeoxyriboNucleic Acid) is the genetic material found in the cells of your body. A person receives half of their genetic material from their biological mother and the other half from their biological father. Paternity testing is performed using a technology called PCR (Polymerase Chain Reaction), in which specific areas of a person’s DNA—called genetic loci—are amplified, analyzed and compared to those of another person to determine whether they share genetic markers in common and whether they are likely to be genetically related. Non-DNA based genetic tests, such as blood typing, are no longer performed for present-day paternity and family relationship testing.

How do you test DNA?

To test DNA for determination of paternity and other family relationships, buccal swab samples are used almost exclusively as the source of the DNA.  Buccal swabs are cheek cell samples that are collected by gently rubbing cotton swabs on the inside of the mouth.  In the laboratory, DNA is extracted from the cheek cells on the swabs and then analyzed using sophisticated instrumentation to identify the donor’s genetic markers at specific chromosomal locations.  Largely due to the fact that they are non-invasive and painless, buccal swabs replaced blood samples as the specimen of choice about 20 years ago.  Today, blood samples are usually only tested if buccal swabs are unavailable.  In the event that buccal swab or blood sampling is not possible, other types of samples may also be tested (see below).

Is a blood test more accurate than a swab test?

There is no difference in the accuracy of DNA tests performed using blood versus buccal swabs. This is because the cells of your cheek (and all other types of bodily tissue) contain the same DNA as the cells of your blood.

How is paternity determined in a DNA test?

The genetic loci analyzed contain DNA sequences known as short tandem repeats (STRs)—short, repeating units of DNA.  For each person, the number of repeats present at each genetic locus is variable and is inherited from their biological parents.  For each genetic locus, each person has two genetic markers, or alleles (alternate forms of the DNA sequence):  one allele is inherited from their biological mother and one allele is inherited from their biological father.

The test result report lists the allele sizes (number of repeats) for the mother (if tested), child, and alleged father at each genetic locus.  By testing the mother, we can determine which allele the child inherited maternally.  The allele that the child received from its biological father (called the obligate paternal allele) can therefore be determined by subtracting the mother’s contribution to the child’s DNA.  If the alleged father does not possess the obligate paternal allele at three or more genetic loci, then he is excluded (ruled out) as the biological father.  If only the child and alleged father are tested, and they do not share any alleles in common at three or more loci, then the alleged father is also excluded.  When the alleged father possesses the obligate or possible paternal alleles at all loci tested, then he is not excluded (not ruled out) as the biological father.  Based on these genetic findings, a probability of paternity is calculated and reported.

How accurate is a DNA paternity test?

Our paternity tests are performed using state-of-the art forensic DNA typing technology and have an accuracy of over 99.9%.

Why can’t DNA tests prove with 100% certainty that a tested man is the father?

A DNA test cannot prove that a tested man is the biological father of a child with 100% certainty because the possibility that the tested man is matching the child due to random chance (coincidence) can never be completely ruled out. However, most courts consider a probability of paternity of 99% or greater as strong and sufficient evidence of paternity. Current DNA test batteries typically produce probabilities of paternity greater than 99.9%.

What is the Paternity Index?

The Paternity Index (PI) is the genetic odds in favor of an alleged father being the biological father of the child. A PI is calculated for each genetic locus, and represents the likelihood that the alleged father contributed the paternal alleles versus an untested, unrelated, random man in the population. The Combined Paternity Index (CPI), which is calculated by multiplying the individual PIs together, summarizes the overall strength of the genetic evidence.

For example, if the CPI is 100,000, it means that the alleged father is 100,000 times more likely to be the biological father of the child than an untested, unrelated, random man in the population. In other words, the chance that he has matched the child by pure coincidence would be 1 in 100,000. If the alleged father does not possess the paternal alleles of the child at three or more loci, then the PI at each non-matching locus is 0, the CPI is 0, and the alleged father is excluded as the biological father.

What is Prior Probability?

The issue of paternity depends not only on consideration of the genetic evidence (the Combined Paternity Index), but on also consideration of the non-genetic evidence, which includes fertility, access of the tested man to the mother, the issue of other possible fathers, etc. As non-genetic evidence is based on events occurring near the time of conception, it forms the basis of Prior Probability, which is the probability of paternity before testing.

To maintain neutrality, laboratories assume that, before testing, the tested man has a 50/50 chance of being the father (i.e. prior probability = 50%, or 0.5). After testing, however, the probability of paternity changes due to the newly-obtained genetic evidence. If the genetic tests exclude the tested man, then the probability of paternity will drop to 0%. If the DNA tests do not exclude the tested man, then the probability of paternity will increase to more than 99%.

How is the Probability of Paternity determined?

The Probability of Paternity is the overall likelihood of paternity expressed as a percentage. It is computed using a mathematical formula that considers all of the evidence in a case—both genetic evidence (Combined Paternity Index) and the non-genetic evidence (Prior Probability). In this computation, the Combined Paternity Index is “converted” to a percentage based on an unbiased assumption that the Prior Probability is 50% (or 0.5)—a neutral value which means that, prior to DNA testing, the alleged father is considered equally likely to be the biological father as he is not to be the biological father. A DNA test result with a Probability of Paternity of 0% means that the alleged father is excluded, or cannot be the biological father. A DNA test result with a Probability of Paternity of 99% or greater means that the alleged father is most likely the biological father.

What if two possible fathers of the child are related to each other?

Because related possible fathers share some of their genetic markers by inheritance, it is more difficult to distinguish between them than between unrelated possible fathers. For example, a man shares 50% (1 out of 2) of his inherited genetic markers with his biological father, brothers, and sons, and 25% (1 out of 4) of his inherited genetic markers with his biological grandfathers, uncles, nephews, and half-brothers. If two possible fathers are identical twins, then genetic tests cannot distinguish them. The standard statistical analysis of the test results assumes that other possible fathers are not related to the tested man. If there is reason to believe otherwise, then this must be brought to our attention so that appropriate testing and statistical analysis can be performed.

What if the alleged father is deceased or unavailable?

If a postmortem blood or tissue specimen from an alleged father has been collected and saved (for example, by a coroner, law enforcement agency, or hospital), it can be tested to determine its suitability for DNA analysis. If a suitable postmortem specimen is not available, paternity can be addressed by testing close relatives of the alleged father, such as his parents, siblings and undisputed children, who will share some of the alleged father’s genetic markers by inheritance.

Can paternity testing be done without the mother?

Yes.  However…

(1) From a scientific standpoint, testing the mother is advantageous because it enables the lab to determine which half of the child’s genes came from her, and therefore which half came from the father.  This increases the conclusiveness of a paternity test.  Although in most routine paternity tests conclusive results are also obtained when the mother is not tested, there are certain situations in which testing the mother is very important and strongly recommended,  Consider a case in which a newborn child is to be tested with an alleged father who has not seen the child before and who is concerned that the mother might substitute another child in order to achieve a desired test outcome.  In such cases, testing the mother enables the lab to confirm that the child tested is indeed hers, because they would match each other genetically.  This type of concern has also been raised in some adoption cases, in which an alleged father seeking parental rights to a newborn child he has never seen is concerned that the presumptive adoptive parent(s) may substitute another infant in the test, with the intention of obtaining a paternity test result that excludes the alleged father.  Including the biological mother in the test eliminates this potential problem.  Finally, because it allows precise determination of a child’s paternal markers, testing the mother is of tremendous value in increasing the conclusiveness of more complex relationship tests, such as sibling tests, grandparent tests, avuncular tests, and tests involving closely-related possible fathers (such as brothers).

(2) From a legal standpoint, for legally-admissible paternity tests, if the mother will not be tested, then consent for testing any minor children (or legally-incapacitated adults) must be provided by the mother, by another adult having the legal authority to provide consent, or by court-order.  Evidence of legal authority or legal guardianship must be provided.

Is there a minimum age for a person to be tested?

No. There is no minimum age requirement to collect a person’s DNA sample. We routinely test newborns and very small infants.

Can paternity testing be done before the child is born?

Yes. Prenatal paternity testing can be performed in two ways: invasively or non-invasively. The most common invasive method involves a procedure called amniocentesis, in which a physician collects (using a long needle) a small amount of amniotic fluid from the womb of the expectant mother between 15 – 25 weeks post-conception. Amniotic fluid contains cells from the fetus but not cells from the mother, and is analyzed using the same established technology as standard (non-prenatal) paternity tests. As a result, paternity tests performed using amniotic fluid samples are fully defensible in a court of law, provided that all samples were collected under a strict chain of custody.  Due to potential risks involved, consultation with an obstetrician is strongly advised when considering amniocentesis.

Non-invasive prenatal paternity testing, a safer alternative which has become available recently, permits detection and analysis of fetal DNA markers using a blood sample collected from the expectant mother on or after 8 weeks post-conception. While accurate, non-invasive prenatal paternity tests have not yet been approved by AABB, have had little exposure in the courts, and thus may not be the better choice if legal admissibility of the results is critical. Prenatal paternity tests are much more costly (usually $500 – $1000 more) than paternity tests performed after the child is born. Health insurance may cover the cost of collection of prenatal samples, but usually only if the procedure is also being performed for medical reasons (such as testing for Down syndrome).

Can DNA testing address genetic relationships other than paternity?

Yes. DNA testing provides general information regarding biological relationships. Thus, questions such as: “Are these two individuals related as full siblings or half siblings?”, “Are the twins identical or fraternal?” and “Do these two individuals share the same maternal lineage?” can be addressed. The amount of genetic information that can be obtained—and the likelihood of conclusiveness of such DNA tests—may vary from case to case. Consultation with our Director is therefore advised before scheduling an appointment for such DNA tests.

Can DNA testing distinguish between identical twins?

No. By definition, identical twins share 100% of their genetic markers, and no genetic test can distinguish them.

Will diet, drugs, alcohol, or medications affect the test results?

No. DNA tests are not affected by food, drugs, alcohol, or medications. There is no need to abstain from eating, drinking or taking medications prior to your appointment, with one exception:  If you are a mother and are breast-feeding a baby who will be tested, please refrain from breast-feeding 30 minutes before the baby’s sample is to be collected.  This is because breast milk contains the mother’s DNA.  If there is residual breast milk in the baby’s mouth when its samples (buccal swabs) are collected, then there is a possibility that the baby’s sample could be contaminated with the mother’s DNA and not produce a clear test result.  If this were to happen, sample recollection would be necessary.

Paternity Testing - Making an Appointment (5)

Do we need a doctor’s request or a court order to get a DNA test?

No. However, we recommend that the parties tested consult with an advisor such as an attorney or doctor, as test results can have significant legal, financial, and emotional consequences. For legally-admissible paternity tests, in the absence of a court order, consent for testing of minor children must be provided by an adult who has the legal authority to do so.

How do I set up a paternity test?

We accept appointment requests by telephone, fax, or e-mail from test participants and/or their legal guardians, legal representatives or referring agency. However, to best ensure that we are provided with the complete and correct identification and contact information, we recommend that the adults who will be tested or who will be providing consent for testing of a minor child or legally-incompetent adult contact us directly. Appointments are usually available the same day or with a few days advance notice. For information on appointment availability in your area, or to initiate a DNA test, please contact us at (714) 648-0468 or send us a message.

Where do I go to have my DNA sample collected?

For our legally-admissible and immigration DNA tests, LB Genetics has an extensive network of over 1,000 sample collection locations throughout the United States and internationally. For information on appointment availability at a location near you, please call us at (714) 648-0468.

For our personal/peace-of mind DNA tests, we will mail the sample collection kits and instructions to you and/or other parties involved.  You would be responsible for collecting the samples (mouth swabs) and returning them to LB Genetics for testing.  If you reside in in Southern California, you may pick up a home collection kit, or have your samples collected, at our Santa Ana office.  We do not provide sample collection services or sample collection kits for personal/peace-of-mind tests at locations other than our main office in Santa Ana, California.  To order a home DNA sample collection kit, please call us at (714) 648-0468.

What if the people to be tested live in different places?

Test participants are not required to have samples collected at the same time and place.  For our legally-admissible and immigration tests, we have over 1,000 collection sites throughout the United States and the world, and can arrange for sample collections at a time and place convenient to each person.  For our personal/peace-of-mind tests, we can ship sample collection kits to test participants located anywhere in the United States.  However, please keep in mind that we cannot verify the origin of samples collected using home kits, so you should be sure that you trust the person(s) who will be submitting the samples before choosing the personal/peace-of-mind testing option.

What happens at the sample collection appointment?

Each person tested (or their legal guardian), will complete and sign paperwork necessary to ensure that proper identification, consent, and contact information is provided. For legally-admissible tests, adult test participants must bring a valid government-issued photo ID and any relevant legal documents (court orders, custody documents, immigration paperwork, etc.), as well as some form of identification for any minor tested children (birth certificate, social security card, photo ID, etc.). For these tests, participants are also photographed and fingerprinted. The entire process (including collection of the samples) usually takes less than 15 minutes for each person tested.

Paternity Testing - Release and Acceptance of Results (5)

When will my test results be ready, and how will I receive them?

Once all samples have been collected, test results are usually available within 3 to 5 business days. Prior to sample collection, we will ask you how you would like us to provide the results to you or to other recipients you wish to designate (such as your attorney). Test results are typically sent by U.S. mail, but may also be provided by email, fax, telephone, or express courier, or may be picked up in person at our Santa Ana, California headquarters.

Can the test results be used for legal purposes?

LB Genetics offers legally-admissible DNA paternity tests and other family relationship tests, which are performed using strict sample identification and chain-of-custody procedures in accordance with the AABB Standards for Relationship Testing Laboratories.  These test results are defensible as evidence in a court of law and are accepted as proof of biological relationship by government or private agencies requiring such verification before granting certain benefits.  These agencies include the Social Security Administration (SSA), Internal Revenue Service (IRS), U.S. Department of State and U.S. Citizenship and Immigration Services (USCIS), U.S. Armed Forces, and Native American tribal membership committees.  For our legally-admissible DNA tests, participants are identified photographically, written consent is obtained, and samples are collected and processed by neutral parties with no interest in the outcome.

Results of our personal/peace-of-mind DNA tests cannot be used for legal purposes.  This is because, for these tests, the identity of the test participants is not verified, and samples are not collected and/or submitted with a documented chain-of-custody by neutral third parties.  For these reasons, we do not state last names of test participants on our personal DNA test result reports.  Peace-of-mind tests are to be used for personal knowledge only.

What information is included with the test results?

For legally-admissible tests, our test results include the following documents:

  1. DNA Paternity/Relationship Test Report.  This document summarizes the laboratory findings, including the genetic profiles of each test participant, the Combined Paternity/Relationship Index and the Probability of Paternity/Relationship.
  2. Declaration of the Custodian of Records.  In accordance with California Family Code 7552.5, this document certifies the identification of the test participants, the collection and chain-of-custody of the samples, the qualifications of the lab Director, and the preparation and authenticity of the test results. This declaration facilitates the acceptance of the results into evidence in a court of law.
  3. Sample Identification and Chain-of-Custody Records.  These documents include the photographs and thumbprints of each test participant obtained at the time of sample collection, and the verification of sample identification, collection, packaging and receipt by the personnel who performed these steps.
  4. Explanation of Results.  A detailed explanation regarding DNA testing and interpretation of the results is included for our paternity and maternity tests.


For immigration tests, our test results include the following documents:

  1. DNA Paternity/Relationship Test Report.  This document summarizes the laboratory findings, including the genetic profiles of each test participant, the Combined Paternity/Relationship Index and the Probability of Paternity/Relationship.
  2. Sample Identification and Chain-of-Custody Records.  These documents include the photographs and thumbprints of each test participant obtained at the time of sample collection, and the verification of sample identification, collection, packaging and receipt by the personnel who performed these steps.  Copies of the identification presented by the test participants (photo IDs, birth certificates, etc.) are also included.
  3. Explanation of Results.  A detailed explanation regarding DNA testing and interpretation of the results is included for our paternity and maternity tests.
  4. Request for Evidence.  When applicable, a copy of the Request for Evidence issued by USCIS, passport agency or other requesting immigration office will be included with the test results that are sent to that office.


For personal/peace-of-mind tests, our test results include the following documents:

  1. DNA Paternity/Relationship Test Report.  This document summarizes the laboratory findings, including the genetic profiles of each test participant and a conclusion statement as to the likelihood of the alleged relationship, including, when applicable, the Combined Paternity/Relationship Index and the Probability of Paternity/Relationship.
  2. Explanation of Results.  A detailed explanation regarding DNA testing and interpretation of the results is included for our paternity and maternity tests.


What is AABB accreditation?

AABB accreditation is the most widely recognized certification for DNA paternity testing laboratories and is considered the gold standard in the industry.  AABB (formerly called the American Association of Blood Banks) establishes rigorous standards of quality with respect to sample collection, laboratory analysis, experience, competence, confidentiality and safety, and ensures that accredited facilities comply with these standards through regular on-site inspections.  AABB is approved by the U.S. Secretary of Health and Human Services as an organization whose accreditation qualifies a laboratory (in most states) to perform chain-of-custody paternity testing for family court cases (involving child support, custody, etc.).
View or print PDF File of accredditation certificateAABB is also approved by the U.S. Department of State and USCIS, which require that DNA relationship tests to be used for U.S. immigration purposes be performed only by AABB-accredited facilities.  If your results will be presented as evidence to any government authority or official tribunal, then you should ensure that an AABB-accredited facility performs the testing.  In so doing, you can be confident that the results are not only trustworthy, but also unlikely to face judicial challenge or rejection.  LB Genetics is proud to be one of the few (less than 40) DNA testing facilities currently accredited by AABB.


What does “Chain of Custody” mean?

In paternity testing, chain of custody is the documentation of the collection, packaging, transport, receipt and analysis of test samples, including the identity of the person(s) who performed each step and the date and location each step each was completed.  Maintaining a chain of custody ensures the traceability of each step in the testing process—from collection of samples to reporting of results—and is essential for the legal defensibility of the results in a court of law.  LB Genetics’ legally-admissible paternity tests adhere to a strict chain of custody, in complete accordance with the AABB Standards for Relationship Testing Laboratories.

Payments & Policies (5)

How much does a paternity test cost?

Our fee for a standard, chain-of-custody (legally-admissible) paternity test, involving one possible father and one child, is $395.  Testing of the mother and sample collection at over 1,000 U.S. locations is provided at no additional charge.  Also, because paternity testing is a service, no tax is added to the testing fee.  Other types of DNA relationship tests may be more or less expensive depending on the nature and complexity of the tests and services provided.  For more information on our fees, please call us at (714) 648-0468.

What kinds of payment options do you offer?

LB Genetics accepts the following forms of payment:  cash, credit card (Visa, Master Card, Discover, and American Express), debit card, money order, cashier’s check, and bank/wire transfer.  Before any samples are collected, payment of at least half of the total DNA testing fee must be made directly to LB Genetics at our Santa Ana, California headquarters.  Payments may be submitted in person, by telephone, by mail, by express courier, or by wire transfer.  Test results will not be released until the DNA testing fee has been paid in full.  All payments made are non-refundable in the event that the test is cancelled or not completed.

Does insurance cover the cost of a paternity test?

In most cases, health insurance (including Medicaid) will not cover paternity testing because it is not considered to be medically necessary.  In some cases, insurance may cover the cost of prenatal sample collection, but usually only if the sample will also be used for medical diagnostic purposes, such as Down syndrome testing.

If one party pays for the testing, why does the other party get the results?

Regardless of who pays for the test, all parties who provide a sample for testing or consent for a sample to be tested are entitled to receive results.  As an independent DNA testing facility, LB Genetics is neutral and will not restrict test results to one person or party (unless specified otherwise by court order or written agreement between the parties providing consent for the test).  Test results are completely confidential and will not be disclosed to outsiders without a court order or the authorization of an individual who has provided consent for the test.

How do you ensure my privacy?

LB Genetics has strict, written policies to ensure that the DNA testing process is private and that client confidentiality is protected.  We will not discuss or provide information about your case to anyone who has not been authorized by you or by other adult parties who have provided consent for the test.  All conversations with test participants are confidential and are not discussed with other test participants or their representatives.  Caller identity is verified before any confidential information—including results—is released by phone.


 By: Dr John Taddie

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