September 19, 2008
Category: personal genomics
Google co-founder Sergey Brin has discovered that he carries a genetic variant associated with an increase in his risk of Parkinson's disease, via a 23andMe genome scan.
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Posted by Daniel MacArthur at 11:42 AM • 3 Comments •
Category: big genetics
This will probably only be of interest to population genetics afficianados, but I just noticed that the HapMap project has made its phase 3 data available through its browser (the data were previously available for download, but are much...
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Posted by Daniel MacArthur at 9:10 AM • 1 Comments •
September 16, 2008
Category: genome-wide association studies
The genome-wide association study has been the technique du jour in human genetics for much of the last two years. It's a pure brute force approach, surveying up to a million sites of common variation throughout the genomes of thousands...
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Posted by Daniel MacArthur at 12:32 PM • 8 Comments •
September 15, 2008
Category: genome-wide association studies
Over the last two years, genome-wide association studies have identified hundreds of genetic variants associated with common diseases - but for most diseases the bulk of genetic disease risk remains unidentified. Where are the risk variants hiding?
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Posted by Daniel MacArthur at 9:02 AM • 5 Comments •
September 11, 2008
Category: whole-genome sequencing
The announcement of the first Arab genome sequence is standard genomics by press release - but it promises some good things to come for human disease genomics, and for biomedical science in the Middle East.
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Posted by Daniel MacArthur at 4:18 AM • 0 Comments •
September 10, 2008
Category: blog admin
Update: Please RSVP on Facebook if possible. Tim Lambert from Deltoid has organised a ScienceBlogs millionth comment party in Sydney. I'll be there as well (albeit probably looking a little frazzled and well in need of a beer, as I...
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Posted by Daniel MacArthur at 11:21 PM • 0 Comments •
Category: bioinformatics
A quick note for bioinformaticians in the audience: Neil Saunders has an excellent post on parsing (i.e. processing a file to retrieve specific sections of interest). Neil's hints are a useful introduction for beginners, but also provide some handy reminders...
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Posted by Daniel MacArthur at 12:18 PM • 0 Comments •
Category: personal genomics
David Hamilton argues that the price cut for 23andMe's genome scan service may in fact herald the demise of the personal genomics industry.
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Posted by Daniel MacArthur at 11:58 AM • 1 Comments •
September 9, 2008
Category: personal genomics
23andMe is one of three companies currently providing chip-based personal genomics assays, which provide information about up to a million sites of common variation throughout the human genome. These companies provide insight into a limited but informative slice of your...
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Posted by Daniel MacArthur at 6:25 AM • 8 Comments •
September 8, 2008
Category: personal genomics
The biotech start-up Knome offers personal genomics for the discerning (and wealthy) customer: a near-complete sequence of your genome for a cool $350,000. Is your DNA worth the money?
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Posted by Daniel MacArthur at 12:01 PM • 10 Comments •