This is a large amount of data not being used by services testing DNA. There are millions of SNP’s contained in your DNA. This type of testing only looks at specific variations. This requires between 100 and 300 AIM’s. This is a small fraction of the SNP’s differentiating DNA. This means if your test stated you are fifty percent European, it means only half of your SNP’s appear to be European. Another issue is certain markers used for ancestry information for any given test are only derived from either your Y chromosomes or your paternal line or your mitochondrial DNA or maternal line. When these markers are used, your test will be less accurate. Another flaw is the DNA testing services are obtaining DNA from the current populations in specific regions. This makes unsubstantiated conclusions that the people living in these areas hundreds of thousands of years in the past have had the same DNA for all these years.
Newman says that there’s a basic lack of “literacy” and understanding about genetic testing, among the public and even other health professionals. People are given false reassurances or made to panic (just because you have certain genetic variants, it doesn’t mean that you will develop a particular condition). Newman also makes the point that, in his field, counselling happens before and after testing and, while people with cancer or heart issues nearly always opt to have the test (as they can then take action to varying degrees), often people with conditions such as Huntington’s disease in their family decide not to go ahead because a diagnosis would change nothing for them. In any event, Newman says that, with genetic testing, while there are different levels, intensive counselling is always “absolutely key”.
Obviously, the more information you can provide, the more results you will receive. But not everyone has access to all of their ancestral information. . Digging up various info about yourself can be time-consuming and downright impossible for some. That’s why it’s important to look for services that are flexible with how much information they’ll require from you.
My own results are eagerly awaited: the whole process takes about 6 weeks. I am somewhat more sceptical having Polish heritage and therefore my contact with relatives might be less likely, however I am waiting eagerly to see whether I have any trace of the Mongol hoards who invaded deep into Europe. I have posted a screenshot of how long the process takes from activation.
Haplogroups are a different story. Your maternal line haplogroup assignment is derived from a separate piece of DNA called the mitochondria. Since mitochondria is passed on only by mothers to their children, your maternal line haplogroup assignment only tells you about your mother's side of the family. Similarly, the paternal line haplogroup assignment is derived from a different, separate piece of DNA called the Y chromosome. The Y chromosome is only passed from fathers to sons and only traces the paternal line.
For better ancestry and medical insights, you should encourage family members, especially parents and grandparents, to take a DNA test as well. If your family is from a specific geographical location for generations, your samples could potentially improve the service's reference panel, in turn improving results for everyone. If you’re female and take a test from 23andMe or LivingDNA, you can view paternal haplogroup information, and you get more information when one of your male family members takes a test as well.
Gteat article! Thank you so much. I am Jewish American. Both sides of my family immigrated from Eastern Europe/Russia about 5 generations ago. I would really like to try and find out more about exactly where they came from, identify potential living and deceased distant relatives in the USA and abroad and ultimately start creating an extensive family tree. Which test would you suggest?
In testing, we found that many tests have much more specific and detailed results for European ancestry than anywhere else. This is due more to the diversity of the database than size. For example, AncestryDNA has the largest database with over 10 million samples yet results for Asian ancestry are markedly less specific than results from several companies with much smaller databases, including 23andMe and Living DNA. Instead of pulling reference samples directly from the existing database, however, many companies seek out high quality data with special research projects. 23andMe, for example, offers its Global Genetics project, which sends free kits to people with all four grandparents born in certain countries that are underrepresented in the database.
We evaluated each kit by ordering one, just like any customer would, and tracking how long it took to arrive at the lab and to get processed. Then we compared the breadth and depth of the results to see what rose to the top. The whole process was a lot of fun, in part because of the anticipation of getting the results. Most of the kits warn that testing your DNA can lead to surprising—even life-changing—results. For example, there's the story of a woman who thought she was Irish, but her DNA test revealed she was also European Jewish, Middle Eastern and Eastern European. After diligent research, she discovered that her father, who had died years earlier, had been switched at birth with another child.
In addition to showing geographic ancestry percentages, some direct-to-consumer DNA tests also include insights about physical traits like hair and eye color. With 23andMe, this trait information is mostly available in the upgraded Ancestry + Health kit, but some interesting tidbits can be found in the Your DNA Family report, which is available if you opt to participate in the DNA Relatives service. This report tells you interesting information, such as that your DNA relatives are 32 percent more likely to own a cat or 11 percent less likely to have lived near a farm when they were young. DNA Passport by Humancode offers information about more than 20 physical traits, from appearance to grip strength. Ancestry DNA recently added its AncestryDNA Traits upgrade for $10, and it lets customers who have already taken one of its tests unlock information about 18 genetically influenced traits, including bitter taste perception, freckles and cilantro aversion.
If you are concerned about your data being sold, your concern may be valid. In the past, records have been sold and de-anonymized. It is possible for genetic information to be used to find the name of the individual the DNA came from. This can happen regardless of whether or not your name was in the database. This scenario has occurred in the past.
I recommend one of two options. It may cost a little more, but I would highly recommend saving the extra and using DNA Tribes® rather than spending over half the cost for minimal tribal/biogeographical pinpointed information. The primary benefit of STR rather than SNP testing is the availability of rich reference data. DNA Tribes® tests industry standard autosomal STR systems, which allow the identification of a person’s DNA profile not shared with any other person. Because these STR markers have been tested and used in the court systems around the world, they allow DNA Tribes® to perform the most thorough comparison of a person’s own DNA profile to over 1,200 ethnic groups (populations) around the world. At present, SNP testing from these other autosomnal DNA testing kits does not yet match the geographical detail of DNA Tribes® autosomal STR analysis.
Following a recent case in Phoenix, in which a patient who had been in a coma for nine years gave birth, Arizona lawmaker David Livingston sponsored a senate bill that would require certain occupations to submit DNA samples along with fingerprints for use by law enforcement. Though Senate Bill 1475 has been updated since its initial draft, it could set a precedent that normalizes collection of DNA samples from everyone, not just those suspected or charged with a violent crime.
The only patients having their genome sequenced are those with certain cancers or rare diseases. In some cases, family members may also be asked to participate. To take part, a patient must first be referred by a consultant, before being taken through an extensive consent process to ensure they know what participation in the project means. As well as the genome sequence, Genomics England asks for access to a patient’s lifetime medical records so that links can be made between their genetics and their individual disease. The NHS has made it very clear that, for many participants, taking part in this project won’t help them treat their disease. But it is hoped that the information they provide will go on to help treat others in the future.