In order to do a hair test for paternity, you need to have hair that still has the roots and follicles still attached. This means, cutting hair and often even taking strands from a brush will not work, you need to pull the hair from your head and look to make sure the hair follicles and roots come attached to the sample. In most cases of a paternity test, five to ten strands of hair with the root and follicles still attached are required in order to do the DNA testing. Hair test for paternity costs more than most other DNA testing and is not as reliable because it is more difficult to extract enough DNA from the follicles.

Genetic DNA paternity testing allows courts and individuals to confirm paternity of a child. Most tests do hold up in court and do provide for accurate results. In most cases tests using hair samples are not legal tests and do not hold up in court as the DNA testing company can not guarantee from whom the sample came. Most people use a clinical facility which offer legal tests, but some receive a home test kit in the mail and send the sample out for testing which are for peace of mind but are not usable in court.

Why do people need a DNA test for paternity? In some cases, genetic DNA paternity testing is done to determine the parentage of a child. This procedure allows courts, parents and other concerned individuals to know who the parents are, whether it is for the mother or the father. This information allows the custodial parent to receive support of the said child. In most states, if you receive any kind of support from the government, you need to know the paternity of the father.

Why do people need a hair test for paternity? In most cases people are trying to determine paternity without the alleged parent knowing. They want to send in a sample of the alleged parent and are unsure of what will work. TV shows make testing with hair seem simple and do not show any of the down sides of using hair. There are many types of samples that can be used and while hair is the most well know it is not necessarily the best. Some more reliable options are Band Aids, Fingernail or Toenail clippings, Dental Floss or a Toothbrush. While the results will likely not be court admissible, unless collected by a third party investigator, they do offer peace of mind.

Before genetic DNA paternity testing helped to identify a father, men who were said to be a father were just that, determined and appointed the father. Today, a simple paternity test will reveal if the individual is the legal father or not. This procedure has also aided in the overturning of many rulings by the courts when confirming that someone was a father, they have been found not to be the father, which leads to hardship for many. Check your state laws on to see what the statutes of limitations are for changing paternity.

Earlier tests conducted used the blood type of the mother and father to determine if the baby belonged to the father. Due to technological advancements the most common from of paternity testing is DNA testing, which is done by using cheek swabs from all parties concerned. Some people feel this could cause a big problem with child support agencies, as they try to collect from the real father after collecting support from the wrong father for years. In many states there are laws limiting the amount of time allowed to change the paternity of a child for that exact reason.

With the advancement of DNA testing, the entire process has helped in many areas as people use the genetic DNA paternity testing to find lost children and find missing fathers. Technology keeps advancing and so does paternity testing.

In conclusion, a home DNA test is a relatively simple and painless procedure and usually involves taking a swab of the inner cheek of both the suspected father as well as the child and, if possible, it’s mother. When choosing a home DNA test kit you should look for a kit that is AABB accredited and which offer a 99% inclusion and 100% exclusion rate. If you need or want to use the results for any legal purposes you should talk to the company offering the test and make sure the test option you choose is a legal test.

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How DNA testing is done depends on the results desired and the samples available. DNA profiling is the process of analyzing and comparing two DNA samples. Only identical twins have the exact same DNA sequence, everyone else’s DNA is unique. This makes DNA the perfect way to link individuals to each other or to locations where they have been.

The entire DNA chain is incredibly long, much to long to examine all of it. Human DNA is made up of about 3.3 billion base pairs. The differences between DNA samples occur only in small segments of the DNA–the rest of the DNA is very similar. DNA testing focuses on those segments that are known to differ from person to person.

As DNA testing has evolved over time, the testing methods have become more precise and are able to work with much smaller DNA samples. Early DNA testing was done using dime-size drops of blood. Today’s tests can extract DNA from the back of a licked stamp (in some cases) but is most often done by using cheek swabs. These cheek swabs are easy to collect, painless and very accurate The DNA must be extracted from whatever sample is provided. DNA must be isolated and purified before it can be compared. In essence, it has to be “unlocked” from the cell in which it exists. The cell walls are usually dissolved with a detergent. Proteins in the cell are digested by enzymes. After this process, the DNA is purified, concentrated, and tested.

DNA testing is done most often today using a process called “short tandem repeats,” or STR. Human DNA has several regions of repeated sequences. These regions are found in the same place on the DNA chain, but the repeated sequences are different for each individual. The “short” tandem repeats (repeated sequences of two to five base pairs in length) have been proven to provide excellent DNA profiling results. STR is highly accurate–the chance of misidentification being one in several billion.

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Regardless of net worth, it is important for all individuals to have a basic estate plan in place.  This can be done with a family attorney or there are many online legal aid sites that can assist you in creating the proper document. Most often the biological children of deceased individuals have inheritance rights, DNA is being used more and more when estates are in question.

In some cases, previously unknown children can appear to claim part of the estate. Or, a greedy or unhappy family members may claim that a beneficiary is not a biological descendant of the deceased person. Depending on the timing of the claim, defending this claim could require exhumation or testing of autopsy specimens, neither of which is a pleasant process and which can be an expensive process.

DNA has emerged as a common tool in modern human identification and has magnificent and unparalleled applications in modern society. The best defense is a strong offense. In many cases proper legal registration of your DNA profile with your estate planner or attorney will help ensure legal and rightful administration of your estate, should the need arise.

The DNA relationship testing market has been growing steadily over the last twenty years.  Prices are decreasing and the easy of testing is increasing. Today, it is projected that the annual number of persons that will participate in some type of paternity or extended relationship test will exceed 1 million. In sharp contrast, it is estimated that less than 200,000 persons were tested in 1988. The increased demand for DNA testing has been fueled by greater public awareness of the power of DNA and the affordability and easy access to testing.

According to the National Center for Health Statistics, 2007 was a record year for births in the United States, there were 4,315,000 recorded births. Experts think that the increase has to do with a range of factors, including immigrants having more children, professional women delaying pregnancy until their 40s and a larger population of women in their 20s and 30s. These factors, coupled with the fact that 38.5% of all U.S. births in 2006 were from unwed mothers translates into an increasing need for education of families about the importance of knowing ones biological parents.

About DNA

DNA is the map of life and defines the essence of our individuality. Despite the size of the human genome, over 3.2 billion genetic markers, 99.9% of the DNA in all unrelated people in the world is identical. Thus, the vast differences observed in the human race are created from the minute differences in only 0.1% of DNA. An individual’s DNA can contain valuable information to help the lives of present and future generations. Locked in our DNA code are the secrets of our ancestry and medical conditions that scientists are only now beginning to understand.

PATERNITY

It is natural for families to want to know who the biological father of their baby is. Nationwide, approximately 30% of tested men are excluded as the biological father.  That means that 3 out of 10 test comes back as a negative result for paternity. A child has the right to the sense of identity that comes from knowing who both biological parents are. Knowledge of a child’s biological heritage is also very important in understanding future possible health risks. In addition, determining paternity gives a child legal right to receive financial support from the father and to inherit from the father.  This is the same if the mother is unknown.  In an era when adoption is a popular option it is important to remember that more and more people do not know either biological parent.

RELATIONSHIP TESTING

Relationship DNA testing can determine if a long lost brother or sister, grandparent, aunt or uncle is truly related to the family in question. DNA testing can also reveal if twins are identical or fraternal. Modern DNA testing can provide answers for a new world of relationships. Paternity testing can also be performed indirectly by testing relatives of an alleged father.

FORENSIC PATERNITY

If a person is deceased or unavailable for testing which is often the case in the question of estate settlement, forensic DNA testing can be an invaluable tool.  DNA can be found on evidence that is decades old. Common sources of forensic DNA evidence include: fingernail clippings, hair with roots or follicles, chewing gum, used beverage containers, eyeglasses, hats, lickable stamps or envelopes, teeth, post mortem tissue, a toothbrush, or cigarette butt.  The results that can be looked for from each item differs and it is best to contact your laboratory to see what items they recommend. For more infomation on DNA testing and how it can asssit you please contact DNA Identifiers.  Remeber regardless of you net worth it is important to have an estate plan in place and DNA can be an important part of your plan.

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I just came across an article distributed by the Slate discussing the above topic. This brought my thinking to the use of DNA and the idea of anonymity in general.

DNA testing makes them easy to trace
By Rachel Lehmann-Haupt Last Updated Monday, March 1, 2010, at 9:36 AM ET

When Donor 3066 signed up with the California Cryobank, he offered some basic information about himself on a piece of paper: that he had a BA in theater; that his mother was a nurse and his father was in the Baseball Hall of Fame; that his birthday was Sept. 18, 1968. He made it clear that he didn’t want to be found by signing a waiver of anonymity…

Donor 3066 was being sought out by Michelle Jorgenson, a 39-year-old waitress from Sacramento, Calif., whose daughter, Cheyenne, was born in 1998.  When her daughter turned 5, Jorgenson joined the Donor Sibling Registry and began searching for other mothers and donor offspring who used Donor 3066. She was concerned because her daughter was sensitive to sounds and walked on her toes, and she wanted to know if other half-siblings were displaying similar behavior. Through the registry, she met a number of other mothers and half-siblings. She discovered that two had autism and two others showed similar signs of sensory disorder…

Jorgenson began her search by approaching a mother in her group with a son named Joshua and suggested he do a cheek swab so she could explore his paternal roots through a Y chromosome test. The mother agreed. Through the test, Michelle learned about some of Joshua’s genetic markers. A few weeks of searching on the Family Tree DNA Web site using these markers led to two families with matching DNA. Through one of the families, she met a woman who mentioned that she found the obit of a relative who was a former baseball manager, and three children were listed. Michelle suspected that this might be her donor’s father, so she looked up the phone number of his listed son. When Michelle called the number, the deceased man’s son answered the phone. She began to ask him questions: Was your father in the Baseball Hall of Fame? Were you born in Illinois? Did you ever donate sperm? When the man said yes, she asked him if his birthday was Sept. 18, 1968. When he answered yes, she burst into tears. “You’re the biological father of my daughter,” she said. He was shocked but agreed to talk to Cheyenne on the phone—and eventually allowed the two to come visit him in Los Angeles.

Although in this case there appears to be a happy out come for all parties this is not always the case.  What about the request for privacy that Donor’s sign up for when they choose to remain anonymous?  Is that even something that clinic should offer since there is no guarantee that the donor can’t be found?  What are the options for men who do become donors?  There are many questions that are raised in this article and very few answers, partly because technology is growing at such a fast rate and party because it appears in the article many clinics are ignoring this issue of privacy.  Let us know what you think about this issue.

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The blood test uses the mother’s plasma to extract Genetic information about their unborn baby. The test can be used to determine if the unborn baby carries specific genetic abnormalities, such as muscular dystrophy, this test can be conducted shortly after conception.

Currently, testing for genetic abnormalities and gender cannot be carried out until at least 9 weeks and as late as 24 weeks. The current methods of testing are either through a Chorionic Villus Sampling (CVS) or an Amniocentesis.

Chorionic Villus Sampling (CVS) is a medical procedure conducted by an OBGYN that is typically performed between 9 – 13 weeks gestational age, which is often mistakenly referred to Chronic Villus (or Villi) Sampling. CVS is a vaginal procedure that removes a very small portion of the placenta.

Amniocentesis is a medical procedure conducted by an OBGYN that is typically performed between 14 – 24 weeks gestational age. The amniocentesis procedure involves insertion of a needle into the womb and drawing out approximately 10cc’s of amniotic fluid, which surrounds the unborn baby.

Professor Michael Chapman, head of women’s and children’s health at the University of NSW, said that this new testing method was the “holy grail” of research. “Scientists have been chasing this for about 25 years,” he said. “The biggest advantage of this in a wanted pregnancy is there is no risk of miscarriage during testing.”

The research team from the University Medical Center, in The Netherlands, used the test on 200 women. Only in 10 cases could the gender not be determined. The procedure works by taking a sample from the mother’s blood plasma and extracting fetal DNA, which circulates in the mother’s blood. Looking for a specific gene sequence, doctors can then determine if the baby is a boy or a girl and is a carrier of specific disorders. In most cases, the test will be performed on a seven-week-old fetus.

But Australian obstetricians warn the medical breakthrough is unlikely to be used in Australia because it could be used for gender selection and due to “ethical and moral” dilemmas.

The test did not address the fact that fetal DNA that is found in a mother’s blood can be from previous pregnancies even years later. The research have not address how to determine if the DNA is from the current fetus. While their are some DNA testing companies that have offered to use “simple” blood test to determine paternity for several years. These test can often be unreliable. While this new test promise great answer at no risk there are still some very big questions that haven’t been answered.

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Fathers still have important rights they need to be aware of: First, it is very important to have the child legally declared to be your child, by DNA Testing, birth certificates, or other methods. Second, all biological fathers are entitled to reasonable rights of visitation and contact with the child, including holidays, school events, report cards, and extra curricular activities and visits to doctors and dentists. Lastly, fathers have the right to have child support set a a reasonable amount based on their financial situation. All states have laws regarding child support, including how to calculate what your child support dollar amount should be.

Any parent can lose custody if they are found unfit due to drug or alcohol dependency, neglect/abuse of the child, or if they fail to maintain a consistent home life for the child. Historically, one of the many arguments for granting a mother primary custody was their constant presence in the the home. This is no longer a valid reason because most women today now work outside of the home and are not the full time care givers.

Today, all parents have a basic right to be awarded full or partial custody. However, certain individuals will jeopardize that right should it be proven they are unfit to parent. Each case is unique and should be evaluated on an individual basis. In some states, this judgment is made by a jury and in other states by a Judge.

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DNA is inherited from our parents, with half coming from the mother, and the other half from the father. This means that when the mother is not in dispute it is best to include her in the DNA paternity test so that you can eliminate the DNA the child inherited from her, this will leave only the DNA that came from the biological father.

The process is relatively simple in that the final DNA profile of the child is composed of a series of bands which can only come from the two parents. If the mother’s bands are deducted from the child profile the remainder must come from the biological father.  Any male that may consider himself the father can have a DNA profile produced and compared against the remaining bands in the child’s profile.

There can only be two outcomes from this type of comparison. The first is an ‘exclusion’ scenario where the remaining bands in the child’s profile could not have come from the sample obtained from the alleged father.  An exclusion eliminates the possibility of this individual being the biological father of the child.  An exclusion is 100% accurate. The second outcome is an ‘inclusion’ in this scenario the remaining bands in the child’s profile could all be accounted for by comparison with the alleged father. If this is the case the strength of the match needs to be assessed by a DNA interpretation expert who will provide a degree of certainty associated with the likelihood that the alleged male is the biological father of the child.  This means that there is no yes answer but rather a probability of paternity typically it is 99.9+%.

Before you purchase any Paternity DNA testing you should be sure you have clear answers to the following 4 key questions:

1. Has the DNA testing facility been accredited by a validated external body such as the American Association of Blood Banks (AABB). If the answer is no, do not have your testing done by this company, you may not be able to rely on the results.

2. Does the company carrying out the DNA testing have a thorough track-record in this area of work? Have they proved their technology in court?  DNA profile interpretation can be a tricky business, and there is a lot at stake when you commission a DNA test, and you want to be able to rely on your service provider.

3. What degree of certainty does the company guarantee in relation to the results of the tests? An exclusion should be 100% with an inclusion at, at least 99.9+% confidence levels. These are the figures that are expected in most courts of law.

4. Does the internal quality standard require duplication of all results before they are reported to the customer? Or more simply put do the run all tests twice? This is an industry standard requirement which is often overlooked by some of the ‘cheaper’ DNA testing providers.

If the answer to any of these questions is unclear, my strong advice is to find an alternative provider. You do not want to trust such an important and life changing test to a company that does not guarantee a top quality product, with excellent customer care back-up.

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UCLA Scientists link genetic variant to autism risk. This discovery may explain the gap in autism cases between boys and girls. Dr. Stanley Nelson, professor of human genetics at the David Geffen School of Medicine at UCLA and his team narrowed their research on a region of chromosome 17 that previous studies have tied to autism. In that region they discovered a variant of a gene (a gene that is essentially the same as another, but has mutational differences) called CACNA1G. Dr. Stanley Nelson and his team looked at the DNA of 1,046 members of families with at least two sons affected by autism for common gene variants.

According to Dr. Stanley Nelson, “We wanted to identify what was happening in this region of chromosome 17 that boosts autism risk. When the same genetic markers kept cropping up in a single region of the DNA, we knew we had uncovered a big clue.”

The researcher team traced the genetic markers to CACNA1G. CACNA1G helps move calcium between cells. They discovered a common variant that appears in the DNA of nearly 40 percent of the population studied.

“This alternate form of CACNA1G consistently increased the correlation to autism spectrum disorders, suggesting that inheriting the gene may heighten a child’s risk of developing autism,” Nelson said, but he emphasized that it cannot be considered a risk factor on its own. “This variant is a single piece of the puzzle,” he said. “We need a larger sample size to identify all of the genes involved in autism and to solve the whole puzzle of this disease.”

This study was funded by the National Institute of Mental Health and Cure Autism Now. The DNA samples were provided by the Los Angeles–based Autism Genetic Resource Exchange (AGRE).

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While positive DNA tests can be accepted as positive evidence of paternity in the most cases due the statistical improbability of potential fathers having the same DNA profiles, if the possible fathers are related  they are more likely to have similar DNA profiles. It isn’t uncommon for brothers to be involved in a parentage dispute, or even for the mother to have a DNA test carried out privately to determine which is the father of her child.

The Legal Aspects

Where DNA paternity testing is to be used in evidence, courts will generally insist on a legal paternity test where the collection of the sampling is carried out by an authorized professional and the identity of the subject legally determined though an ID check and photo documentation. Home DNA testing, or DNA tests on samples presented by the subject, are not admissible as evidence. The probability of paternity accepted as definitive proof varies from state to state, although most states require a probability of 99%.

Such probability is determined largely by the DNA, and the manner the test is preformed. A good DNA test looks at 16 genetic markers, it would run all tests twice independent of each other, and should guarantee resutls of 99.9+%. It also depends on whether the sample of the Mother is included in the testing or not, as this will help to obtain a much higher level of probability.

Common DNA between Family Members

DNA tests on related potential fathers are no different from those carried out on any other subject: it is the results that could potentially create problems. Take the case of first cousins: they share 12.5% of their DNA and so it will be more difficult to prove parentage. This sharing of DNA increases to 25% for uncles, nephews and half-brothers, and to 50% for sons, fathers and brothers of the person being tested.

DNA paternity testing on different members of the same family is not an uncommon situation, and can occur for a number of reasons, including:

a) Pregnancies arising from consensual and non-consensual relationships with related men.

b) Two family members each claiming parentage, whether or not the mother is claiming one or neither to be the father.

c) A brother desiring confirmation that he is the parent.

d) The mother, or potential mother, having a private test to assure herself as to who is the father.

e) A grown child confirming parentage, particularly where an inheritance could be involved.

There are others, but these are common reasons for legal and home DNA tests being carried out where potential fathers are related. Standard DNA paternity testing statistics are based upon unrelated members of the public, and unless the laboratory carrying out the DNA testing has been informed of the relationship, the test results could be misinterpreted.  Most reputable DNA testing companies will recommend that you preform a paternity test with each of the potential fathers to verify which would be a closer match to the child.

The Case of Identical Twins

Nevertheless, it is possible to test additional DNA markers if any of the above relationships are known, but not in one specific case. This is the case of identical twins.  Fraternal twins occur when two eggs are fertilized by two sperm, and are no more alike genetically than were they siblings born years apart. Identical twins, however, are formed when one egg is fertilized by one sperm and then splits into two halves within the first 14 days for no known reason.

These twins share an identical DNA their DNA profiles would be indistinguishable from one another. There is no test that can determine which is the biological father of a child. Unless one is excluded for some reason, either could be the father and that is all that DNA testing can prove. The court would have to disregard DNA results and use other means to determine paternity.

Old-fashioned policing, therefore, still has a part to play where the related potential fathers are identical twins. Apart from this specific case, DNA paternity tests are not entirely foolproof since they rely on probability, but are virtually conclusive where you simply want confirmation of paternity. In such a case, a likelihood of 1 in a 1000 is a virtual certainty and where confirmation is required between a limited number of candidates, a 99.9% DNA genetic testing result is legal confirmation.

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