Tag: ASHG 2012


November 13, 2012

Expect the Unexpected: Rare Mutation Frequencies

blogger-emily

23andMe’s genetic health reports cover 191 rare genetic mutations in addition to more common variants related to disease. While it’s relatively easy to learn about common variants, our knowledge of rare mutations traditionally has come from very small studies limited to specific populations, like French [...]

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November 9, 2012

23andMe’s Presentations at ASHG

geneticresearch7

This week our scientists have been busy at the American Society of Human Genetics Annual Meeting in San Francisco. As promised we're putting up links to each of the posters that we presented at the meeting. It gives you a sense of the breadth and depth of 23andMe's research and our commitment to share our [...]

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November 6, 2012

Improving the Experience of Participating in Research

JoyceTung

(Editor's note: Here is a link to Joyce's poster presented at ASHG.) Genetic research often requires people willing to share their time and answer questions for the sake of scientific inquiry.  Any study involving research participants should ensure that such volunteers are treated fairly and ethically. [...]

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November 5, 2012

Whole-Genome Sequencing of Parkinson’s Patients

CoryMclean

(Editor's note: Here is a link to Cory's poster presented at ASHG.) Parkinson’s disease (PD) research has long been a priority at 23andMe. Our Parkinson’s research community is one of the largest in the world with over 9,300 patients.  Our research on the disease has been published in peer-reviewed [...]

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November 2, 2012

23andMe Moves into the World of Sequencing

Eharrington

(Editor's note: Here is a link to Eoghan's poster presented at ASHG.) People often use the terms “genotyping” and “sequencing” interchangeably, but they are quite different ways of approaching genetic data. One large difference is the amount of data generated. Genotyping, what 23andMe does, [...]

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November 1, 2012

Investigating the Rare

23andMe-Brian-049

(Editor's note: Here is a link to Brian's poster presented at ASHG.) Rare events are hard to study, and this is especially true in genetics. Imagine you have a group of four people carrying a mutation and two of them are also afflicted with same medical condition.  Coincidence or correlation? Well, this [...]

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October 26, 2012

Researcher Investigates His Own Genetic Mutation

23andMe-Arnab-035

What would you do if you found out that you had a rare and possibly life-threatening genetic mutation? You’d probably talk to relatives about your family medical history.  You’d likely visit your doctor and maybe a specialist.  You might even change your diet and exercise routines. Arnab Chowdry did all [...]

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October 9, 2012

The Genetics of Nearsightedness, Stretch Marks, and Motion Sickness

Amy_Kiefer V4

Amy Kiefer is a Survey Research Manager at 23andMe. She joined the company in 2008. What do nearsightedness, stretch marks, and motion sickness have to do with each other? They don’t appear to be genetically related — at least not according to our in-house statistical geneticists — but all of them are [...]

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