Genealogy > Thom(p)son DNA Project

23 and me and FTDNA pricing change/sales

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They did say they received my sample...which is good. I guess it'll be about 6 weeks for results.


boy. Six weeks is a long time.

Well, it gave me some time to see what I'll get and won't get. I won't get my Y str markers, but that's okay because I've already gotten them from and I don't match anyone close enough to worry about it yet anyway.

I should get my Y haplogroup and subclade which can give some idea of general location in the world. I'll also get my maternal DNA which will give me information on my moms back to my all-mother. 23 and Me has a service like family finder at FTDNA that should help me search for genetic cousins on all sides and hopefully I can load those results up into GEDmatch and meet up with FTDNA participants there.

I still recommend people test with FTDNA to get the most information and to be able to work with the most other people. I'm just cheap and the $100 deal at 23 was too good to pass up.

Along those lines I see that (run by DNA Heritage) is redirecting straight to FTDNA with a message about it's operations transitioning. Hopefully DNA Heritage customers will have their records moved!

I can't wait.  It will be interesting to see if we connect through Gedmatch.

Genetic test maker 23andMe stops marketing after FDA warning

(Reuters) - Home genetic test maker 23andMe, which is backed by Google Inc, stopped marketing its products last week after the U.S. Food and Drug Administration warned that it did not have regulatory approval to do so, a company spokeswoman said.

The company stopped television, radio and online advertising for its $99 DNA test which is supposed to detect a range of genetic variants and provide information about a person's health risks, the spokeswoman said.

The FDA said last week it had sent a warning letter to the company on November 22 stating that products designed to diagnose, mitigate or prevent disease were medical devices that required regulatory clearance.

The agency also said false positive tests for certain breast or ovarian cancers could lead a patient to undergo preventative surgery including mastectomy, intensive screening or other potentially risky procedures. A false negative could result in a failure to recognize and act on an actual risk.

Company founder Anne Wojcicki said in a November 26 blog post that the company had been talking to the FDA since 2008 and had submitted its first application for clearance in July last year, followed by another submission in September.

She said the company had received feedback on the submissions and was behind in its responses.

"We stand behind the data that we return to customers - but we recognize that the FDA needs to be convinced of the quality of our data as well," Wojcicki wrote in the post.

The FDA in its warning letter described those applications as withdrawn because the company had not responded to requests to provide additional information.

(Reporting by Caroline Humer; Editing by Stephen Coates)


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