Bill Newman, professor of translational genomic medicine in the Manchester centre for genomic medicine at the University of Manchester, and chair of the British Society of Genetic Medicine, says that such tests in this context simply don’t make sense and that, usually, telomere testing would only be used in in-depth studies of ageing and diseases associated with ageing. “There’s some really brilliant work going on, by some of the best biologists in the world,” says Newman, citing Elizabeth Blackburn, who won the 2009 Nobel prize for medicine for her work on telomeres. “But there’s no evidence whatsoever that measuring a person’s telomeres gives any indication about their health – or beauty, intelligence, or anything else that might be listed on these sites.”
Product Price Overall Rating Cost Ancestry Results Ease of Use Online Database Features Upgrade Option Available Geographic Regions Database Size Tester Confidence in Results Tester Satisfaction Score Overall Experience Score Sample Type Sample Collection and Registration Score Result Access and Interpretation Score Turnaround Time (Days) App Genetic Relative Connections Online Family Trees Upload RAW Data Download RAW Data
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?
Guidelines recommend that women with a BRCA1 or BRCA2 variant should be screened for breast cancer earlier and more often. Risk-reducing surgery or medication may also be offered. Men with a variant should be screened for breast cancer. Screening guidelines for prostate cancer vary. This test is not a substitute for visits to a healthcare professional for recommended screenings. Results should be confirmed in a clinical setting before taking any medical action. It is important to talk with a healthcare professional before taking any medical action.
We provide expert advice and support in all aspects of DNA testing: paternity, maternity, siblingship, ancestry, DNA storage, and forensic consultancy. DDC has a large legal services client base and provides a comprehensive range of services which includes arrangement of sample collection, chain of custody, quality assurance, and assistance in the interpretation of results, backed by a dedicated customer support team and overseen by the company’s full time geneticist.
Otherwise, the home-testing kits could be said to fit in with our increasingly health-conscious and, if you wish to be cynical, narcissistic times. What says you’re “special” more than finding out everything about yourself, right down to the nitty-gritty of genetics? In this way, these kits could be viewed as the latest plaything of the “worried well”. You could see how the scientific approach would appeal to the health-obsessed of all sexes and ages, your marathon runners and serious gym-goers, who take their fitness extremely seriously.
Our Ancestry Service helps you understand who you are, where your DNA comes from and your family story. We analyse, compile and distill your DNA information into reports on your Ancestry Composition, Ancestry Detail Reports, Maternal & Paternal Haplogroups, Neanderthal Ancestry, Your DNA Family and provide a DNA Relatives tool to enable you to connect with relatives who share similar DNA.
Our testers received notifications that our samples were received 15 days after we mailed them. The email also said that it would take approximately six to eight weeks from that point for results. It actually only took 17 days after the email to get our results notifications. From mailing our samples back to collection, all in all, was 32 days. This was slower than several other DNA services, including the speedy MyHeritage DNA, which had a 16-day turnaround.
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).
Some ethnicity DNA tests will report on the percentage of your autosomal DNA that can be linked to Neanderthals and/or Denisovans – these are non-human ‘hominin’ species that inter-mixed with humans before dying out tens of thousands of years ago. The percentage of our DNA that originates from hominins is 1-5% and it varies greatly between individuals. Only a few genetic ancestry companies include this analysis in their tests (e.g. 23andMe and National Geographic’s ‘Geno 2.0’) and it can be fun to see how much of these ancient species still live on in your genetic code.
1. Family Tree DNA’s Family Finder: One of the first to offer these types of tests, FTDNA is generally considered the leader in autosomal DNA testing for ancestry and provides some of the best tools available for genealogists. Their population finder section is currently a bit less specific than the other companies, but FTDNA Family Finder users are eagerly awaiting a much improved update to be released sometime in the next month. Find out about Family Finder here.