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posted by Fnord666 on Wednesday June 28 2017, @08:21AM   Printer-friendly
from the don't-fear-the-sequencer dept.

Don't be scared. It's just one little genome:

Advances in technology have made it much easier, faster and less expensive to do whole genome sequencing — to spell out all three billion letters in a person's genetic code. Falling costs have given rise to speculation that it could soon become a routine part of medical care, perhaps as routine as checking your blood pressure.

But will such tests, which can be done for as little as $1,000, prove useful, or needlessly scary?

The first closely-controlled study [DOI: 10.7326/M17-0188] [DX] aimed at answering that question suggests that doctors and their patients can handle the flood of information the tests would produce. The study was published Monday in Annals of Internal Medicine.

"We can actually do genome sequencing in normal, healthy individuals without adverse consequences — and actually with identification of some important findings," says Teri Manolio, director of the division of genomic medicine at the National Human Genome Institute, which funded the study. Manolio wrote an editorial [DOI: 10.7326/M17-1518] [DX] accompanying the paper.


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  • (Score: 4, Interesting) by Immerman on Wednesday June 28 2017, @12:16PM

    by Immerman (3985) on Wednesday June 28 2017, @12:16PM (#532390)

    Yours - not a whole lot.

    But how about doing a full sequencing of *all* the DNA in your bloodstream? Every pathogen, parasite, and symbiote sequenced and categorized. No more trial-and-error about figuring out what's causing your symptoms, or at least far less - we know you're carrying pathogens A, D, and R which might contribute to your symptoms, and that D has been present in your last several tests without causing apparent problems, so it's probably A and/or R that are the real problems.

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