Everyone knows that I think 23andme provides a great service. But I’ve had some criticisms in the past. Several years ago I thought it was rather strange of them to […]
As most of you know 23andMe is no longer providing health interpretation services, though they are still providing genealogy (and are unrolling a more advanced ancestry painting right now). You […]
First, download your 23andMe raw results now if you have them. If you don’t know what’s going on, the FDA has finally started to move aggressively against the firm. Unfortunately […]
Earlier editions: Using your 23andMe data: exploring with MDS Using your 23andMe data in Plink From Reconstructing Indian Population History: …We hypothesize that founder effects are responsible for an even higher […]
Note: please read the the earlier post on this topic if you haven’t. The above image is from 23andMe. It’s from a feature which seems to have been marginalized a […]
With the recent $99 price point for 23andMe many of my friends have purchased kits (finally!). 23andMe’s interpretive results are pretty rich now, but there are still things missing. There […]
At this point if you have spare cash why not shell out $300 for a raw copy of your genotype? (yes, I know 23andMe provides other services) I’m sure many […]
As they say, read all about it. I’m rather ambivalent. 23andMe has a business rationale to go in this direction, so I don’t begrudge them their decision. The problem, at […]
Michelle tipped me off to 23andMe’s new initiative to get Parkison’s disease sufferers genotyped. Basically, if you are a sufferer, you get the service for free. The goal presumably to […]
From OpenSNP: At the end of last year we announced that we’ve got some funding from the German WikiMedia foundation to get more people – who are willing to share their […]