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Genetic Future

Commentary on human genetics and evolution, direct-to-consumer genetic testing, and the personal genomics industry.

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Daniel MacArthur
I write about the genetic and evolutionary basis of human variation, and the companies trying to sell you information about your genome.

Daniel also blogs about personal genomics at Genomes Unzipped.

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Consumer Genomics:

Genomic Science:

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September 19, 2008

Google co-founder at increased risk of Parkinson's, according to 23andMe

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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HapMap phase 3 data available for browsing

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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September 16, 2008

David Goldstein on the failures of genome-wide association studies

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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September 15, 2008

Why do genome-wide scans fail?

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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September 11, 2008

First Arab genome sequenced

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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September 10, 2008

Millionth comment party in Sydney on 17th September

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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10 hints on parsing

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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Cheap personal genomics: the death-knell for the industry?

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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September 9, 2008

Cheap as chips: 23andMe slashes the price of personal genomics

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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September 8, 2008

Is a personal genome sequence worth $350,000?

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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