This thread is entitled 'Is 23andMe the most accurate DNA testing company?' hence I refer to accuracy, ancestry and autosomal testing. FTDNA's accuracy regarding yDNA and mtdna testing is better whereas its individual SNP testing, Walk-Through-The-y and overall support to its customers makes for better accuracy in interpreting and reaching further downstream in both y and mtdna terms.
You are basically dodging my comments. You are not answering nor even considering my point of view. You just push on with the same pro-FTDNA propaganda as if your life depended on it.
I didn't reply to this thread at first when I saw the title question because it seemed like a dumb question to me. Unless one company has more no-calls or mis-reported results, all of them have the same level of accuracy. Note that both 23andMe and FTDNA FF use the same
Illumina OmniExpress platform, and therefore equally accurate. This is the only valid answer to the question of
accuracy. FTDNA just customized their chip to remove Y-DNA and some other SNP's so that they could keep charging customers for separate tests.
If you would like to test for medical reasons then I would recommend 23andMe, however the accuracy or correlation between prediction and actual long-term manifestation of predicted conditions are not proven and are considered highly speculative. So if somebody find out they have a 1.2x greater chance of suffering a heart attack, what is the use of this information?
You are confusing accuracy with quantity of information. A calculator that can only do basic additions, subtractions, multiplications and divisions is accurate. A PC that can do all that plus plenty of more things is just as accurate but will be more informative.
FTDNA has five kinds of tests :
1) an SNP test like 23andMe (but less informative than 23andMe because it has 290,000 SNP's less)
2) various STR tests for Y-DNA, useful mostly for genealogists who have relatives who tested
3) custom SNP tests for Y-DNA, which are useful only for people who want to know which brand new deep subclade they belong to.
4) HVR tests for mtDNA which are highly inaccurate and should never be recommended for any purpose. This was one of the first tests I ordered 4 years ago, and the "exact matches" provided by FTDNA turned out not to belong to the same subclades as me at all ! In fact this test couldn't predict my subclade at all, just my mtDNA haplogroup.
5) the full mitochondrial sequence test, which costs more than the 23andMe test and in most cases won't be more informative as 23andMe already tests 90% of the known subclades. Anyway mtDNA is not very informative about ancestry or historical migrations at present, and certainly not useful for genealogy since I have many full sequence matches that are completely unrelated to me, with a long paper trail backing this on both sides.
What would you rather want to know about yourself? That you belong to a specific subclade found in a specific group of individuals or that you have a mildly higher chance of developing a specific form of cancer. Shouldn't you live a healthy life-style regardless and wouldn't most people find health predictions difficult to interpret, process and express to their significant others?
You seem to be unaware that 23andMe also reports carrier status for genetic diseases, for which the likelihood of having the disease or condition is often 100%. This is
very useful to know, as some things that could have afflicted you for years can finally be identified (and in some cases treated). Then, there are many other SNPs that give greatly increased/reduced risks of having a disease or condition. A famous one if the
APOE4 version of the APOE gene, which dramatically increases the chances of having Alzheimer's disease.
You actually referred to y-search and other tools as well.
Confidentiality is about knowing your name, not knowing some anonymous medical data. I am less comfortable about sharing my name on Y-search than sharing my 23andMe raw data anonymously with strangers.
What could happen you ask? Should we not ask what is in the best interest of the customer instead? No company or researcher should be privy to this information without following standard ethical protocol!
Are you saying that 23andMe does not follow any ethical protocol ?
You assume that anonymity relates soley to an individual's last name, is this still the case or will this remain the case into the foreseeable future?
What do you mean ? If you are worried about governments collecting DNA from all its citizens, making a huge database, and testing every surface you touched to follow your every movement in your life, that is paranoia (and unrealistic at that, since no government as the financial means to pay for all these tests, nor any interest in doing so. Even if they did I still wouldn't feel threatened as I am a model citizen).
Am I paranoid for considering the potential harmful effects of this kind of testing? What would you feel like if you found out that you carried the SNP for early-onset dementia or Alzheimers? Would you want to know whether your children carry it and how would your life be effected/affected? If your medical information was used by a company without your knowledge, would you like it?
Not only would I want to know all about it, it was also one of my motivations in taking the 23andMe test. Not knowing is what tends to worry me. The first thing I did when I got my results was checking for the conditions/diseases I was
most afraid of, and it did appease me.
You have found it difficult getting people tested right?, even when providing the funds yourself, because most people inherently know that there is a risk involved, the risk is personal and often has to do with mental health aspects of finding out about oneself. Like it or not, this is the norm rather than the exception. So if I'm paranoid then so are most people.
And that was just for Y-DNA. But French speakers are often extremely wary of DNA tests. It's a cultural thing, and it explains why there are so few results from France compared to Britain, Germany, Italy or Spain, and why there is such a huge gap in the number of results between French-speaking and Dutch-speaking Belgium.