Some concerns about the ultimate efficacy of certain home tests seem to emanate from the industry itself. I did a telomere-measuring test (a mouth swab) by Titanovo, based in north Colorado, which came back saying that my telomeres were too short, putting me at 10 biological years older than I am. However, when I contacted Titanovo, it explained that it had stopped telomere measuring and was now concentrating exclusively on its DNA-utilising “bioinformatics” health, fitness and wellbeing website (analysing client data from other genetic testing sites).
All this comes into sharp focus with the comprehensive kits such as the one provided by 23andMe: the one I drool into a tube for (incidentally, 23andMe doesn’t test for Huntington’s disease). Most people, like myself, have a low understanding of genetic variants, what phrases such as “higher risk” or “probability” actually mean or how to interpret our results correctly. Is it right that ordinary members of the public must navigate potentially frightening and/or misleading results alone?
I decided to take the plunge and purchased an AncestryDNA test before Christmas when it was on special offer with free delivery at only £40. When you consider that what you receive in the Kit is a plastic tube with a bit of blue liquid and en envelope to send it back to them, I am glad I did not pay more as these tests are still in the 'baby' fazes of DNA testing and subsequent discussions with people who are experts in the field have discovered that Ancestry is at the bottom of the rung. Of course the test is done in a Lab and people have to be paid, but the standard fee of £80 + shipping is way overpriced.
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.
A few of the DNA tests we tested, including the National Geographic Geno 2.0, use genetic sequencing instead of genotyping. Sequencing is newer in the mainstream direct-to-consumer DNA testing market, as it used to cost more and take much longer to sequence a person’s DNA. Sequencing identifies the exact makeup of a certain piece of DNA – be it a short segment or the whole genome. The Helix tests sequence the Exome, which are the parts of the genome responsible for protein production, plus several other regions of interest. DNA sequencing gives more information overall and has more uses in medical testing than genotyping. In the future, more DNA kits may move from genotyping to DNA sequencing as the technology gets cheaper and faster, but for now both are effective ways to look into your geographic ancestry.
EasyDNA UK specialises in providing DNA tests that are affordable, accurate and confidential. Our home paternity test is on special offer at just £99 for a limited period. There are NO EXTRA FEES. Sample collection is performed using our easy-to-use DNA test kit. Your DNA paternity testing results are ready in only 3-5 working days. We also offer the option of getting results in 3 working days with our express service (from receipt of samples at the laboratory). EasyDNA tests 21 genetic markers for total accuracy so you can have the peace of mind that you need. A home paternity test provides a 99.99% accurate result if the alleged father is the biological father and a 100% accuracy if he is not.
An ancestry DNA test uses a saliva sample to determine which areas of the world your DNA can be traced back to. DNA kits have become very popular during the last few years. This has led to many people having numerous questions. You may be wondering if your genetic information will be used for research or sold and how this impacts your privacy. You may also be concerned regarding the accuracy of this test or have numerous additional questions. The first thing you must realize is the question of your DNA is complex and there may not be a simple answer. The majority of people in the world have DNA from numerous different regions. You may perceive this combination as unique or you may see it is odd. Either way, you need to be open and prepared for a surprise.
It could be that, in the main, genetic-testing kits such as these could, if promoted and used responsibly, end up zoned completely away from legitimate science and medicine and placed where perhaps they belong, firmly in the lifestyle-extra zone, if and when people think they’re “worth it”. Though, somewhat tellingly, when I ask Newman if he thinks that any of the genetic testing kits are worth buying, he instantly says: “No. I’d say, go to the cinema, watch some sport. Spend the money on something nice, something life-enhancing.”
There are mixed reactions to the use of ancestry DNA databases in criminal cases. On one hand, the rise of readily-available DNA information for millions of people has led to the arrests of several suspects related to long-cold cases, including the arrest of the Golden State Killer. On the other hand, law enforcement accessing private databases of genetic information from consumers raises several questions regarding privacy and ethical issues.
The companies providing ancestry DNA tests are making most of their money from selling the genetic information as opposed to running the tests. Companies purchase this information to increase the size of their genetic databases. Nearly half the companies selling ancestry information are selling to more than just one company. These are sometimes pharmaceutical companies attempting to understand how specific human genome sections can help develop new drugs. Certain mutations will impact the effectiveness of these drugs. The original DNA sample is only destroyed by roughly ten percent of these companies. Most companies keep or sell the sample. This means it is both your data and saliva being sold.
Note that DNA testing isn't the only kind of kit that collects physical evidence from you these days. Ubiome is one noteworthy example. The service evaluates your microbiome—basically the bacteria that live in and on you. In our review, we took its gut biome test, which required our intrepid reviewer to send in a poop sample (insert poop emoji here).
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.
Although the project states that most participants won’t receive any useful information, patients will be told if something is found in their genome that is relevant to the treatment, explanation or diagnosis of their condition. They can also choose to learn if they have a genetic risk factor for another disease, such as the BRCA1 gene mutation that can cause breast cancer. Genomics England will only look for risk factors that are linked to a disease that can be treated or prevented. Untreatable conditions, such as Alzheimer’s, are not looked for.
Your review of the various testing companies is misleading and incomplete. The only test that can give information about recent relatives ( 5 generations back only) is the autosomal test. The others only give our ‘deep’ roots out of Africa migration thousands of years ago. But for the autosomal test to provide us names with whom we can contact, we have to give permission to have our email and name listed (and of course so do others). The tests that say we are such-and-such % of this or that ethnicity isn’t very accurate because, keep in mind, the wars and the spoils of wars that humans have been engaged in forever, mean we all have a mixture of genetic material from around the world. I can tell that the author(s) of this review did not really understand what these tests are about.
Some services include shipping costs in the cost of the kit; AncestryDNA's $99 fee includes two-way shipping. National Geographic's Genographic Project ships the kits for free, but you have to purchase postage when you send your kit to their lab. 23andMe tacks on a two-way shipping fee of $9.95 for the first kit and $5 for each additional one. HomeDNA includes a prepaid envelope to return your sample and offers three shipping options: $7 for two-day shipping, $14 for overnight, and free shipping that takes 7 to 12 business days. Finally, MyHeritage charges $12 for shipping; if you order two kits, you pay $6, and if you order three or more, you get free shipping.
As a postscript, I eventually end up having an interesting chat with Titanovo about my “bioinformatics” (distilled from my 23andMe data). One of the first things I’m told is that my eyes are green (they’re brown). However, the bioinformatics got my skin type and frame/weight generally right and had interesting (albeit occasionally generic) things to say about exercise, diet, goals, steering clear of too much sugar and so on.
While men can trace both their maternal haplogroup (from mitochondrial DNA) and their paternal haplogroup (through the Y chromosome passed down from their father), women can only trace their maternal haplogroup (through the mitochondrial DNA passed down from their mother). This is because the paternal haplogroup is traced through the Y chromosome, which women do not inherit.