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I wonder, does that mean anyone who's already submitted a sample to 23andme will get these reports, or is a new sample required?
by CaliforniaKarl 10y ago
I wonder, does that mean anyone who's already submitted a sample to 23andme will get these reports, or is a new sample required?
- jjeaff 10y agoIf you have already submitted a sample, you will get a report. Since 23andme maps your whole genome, they simply compare the existing data as new finding are approved. OR if you are like some and signed up early before the FDA crackdown, you already got all this information and now they are just reappearing little by little.
- Animats 10y agoSince 23andme maps your whole genome... They don't go that far. A full genome sequencing costs around $2900 as of 2015. (Which is amazing, since the first one cost billions.) Maybe $1000 with the new Illumina HiSeq X Ten sequencing system. Data from a full genome sequencing is about 80GB. (Opportunity here for specialized compression - 98% of the genome for humans is the same.) 23andme is testing for about 100,000 known patterns using a much simpler approach for about a tenth of the price.
- nojvek 10y agoWhere can I get my full genome sequenced?
- Animats 10y agoLots of places. Genomics Personalized Health in Santa Monica offers the service to individuals for $2500.[1] Includes cloud storage for the data. They have a list of medical consultants who can help interpret the data; they just give you the bits. List of service providers.[2] [1] https://genomicspersonalizedhealth.com/ https://genomicspersonalizedhealth.com/ [2] https://www.scienceexchange.com/services/whole-genome-seq https://www.scienceexchange.com/services/whole-genome-seq
- crispyambulance 10y ago23andMe uses genotyping. IANAMB, but I think that means they run a series of assays each of which "examines" a small PART of the genome to look for something very specific. As part of their process, however, they could extract the DNA and keep a sample frozen for later assays or even full genome sequencing but I don't know if they do that. https://customercare.23andme.com/hc/en-us/articles/202904600-What-is-the-difference-between-genotyping-and-sequencing- https://customercare.23andme.com/hc/en-us/articles/202904600...
- cjbprime 10y agoThey give you the option when you sign up, of retaining your sample for later sequencing runs on newer/more comprehensive hardware, or discarding it.
- ksenzee 10y agoFrom https://customercare.23andme.com/hc/en-us/articles/202907980/ https://customercare.23andme.com/hc/en-us/articles/202907980...: "Current 23andMe customers will be notified directly on their eligibility for receiving new genetic health risk reports." Sounds like it depends on which package you bought.
- manmal 10y agoI'm 99.9% sure that a new sample is not required. All of those risk factors can already be looked at with other tools which import raw data from your 23andme account. Eg Promethease evaluates hundreds of genes (both the risks and positive traits) for a couple dollars: http://snpedia.com/index.php/Promethease http://snpedia.com/index.php/Promethease
- BurningFrog 10y agoNow they sell people only "ancestry" report for half the (now doubled) price. They probably don't get it, but I expect everyone on a "full" plan does. They already have the DNA info.
- wavefunction 10y agoI got myself tested years ago with 23andMe and you do indeed get ancestry reports. I also get 'pings' every so often from likely distant relatives (3rd-5th cousins if anything). One lady had been adopted as an infant and was desperately seeking any sort of relative who could tell her something about her origins. I told her what I knew about the families I am descended from but man did I feel bad for her. We were likely distantly related and I'm not sure my info helped, but that would be a pretty remarkable upside to genetic testing for people who want answers.
- selimthegrim 10y agoI was actually able to almost completely solve the mystery of where my great-grandmother came from (adopted as a baby in the South in the early 20th century) using genetic testing.