The $1,000 Genome: The Revolution in DNA Sequencing and the New Era of Personalized Medicine - Hardcover

9781416569596: The $1,000 Genome: The Revolution in DNA Sequencing and the New Era of Personalized Medicine
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In 2000, President Bill Clinton signaled the completion of the Human Genome Project at a cost in excess of $2 billion. A decade later, the price for any of us to order our own personal genome sequence—a comprehensive map of the 3 billion letters in our DNA—is rapidly and inevitably dropping to just $1,000. Dozens of men and women—scientists, entrepreneurs, celebrities, and patients—have already been sequenced, pioneers in a bold new era of personalized genomic medicine. The $1,000 genome has long been considered the tipping point that would open the floodgates to this revolution.

Do you have gene variants associated with Alzheimer’s or diabetes, heart disease or cancer? Which drugs should you consider taking for various diseases, and at what dosage? In the years to come, doctors will likely be able to tackle all of these questions—and many more—by using a computer in their offices to call up your unique genome sequence, which will become as much a part of your medical record as your blood pressure. Indeed, many experts are advocating that all newborns have a complete genome analysis done so that preventive measures and preemptive medicine can begin early in life.

How has this astonishing achievement been accomplished? And what will it mean for our lives? To research the story of this unfolding revolution, critically acclaimed science writer Kevin Davies has spent the past few years traveling to the leading centers and interviewing the entrepreneurs and pioneers in the race to achieve the $1,000 genome. He vividly brings to life the extraordinary drama of this grand scientific achievement, revealing the masterful ingenuity that has transformed the process of decoding DNA and delivering the information it possesses to the public at large.

Davies also profiles the future of genomic medicine and thoughtfully explores the many pressing issues raised by the tidal wave of personal genetic information. Will your privacy be protected? Will you be pressured, by insurance companies or by your employer, to get your genome sequenced? What psychological toll might there be to discovering you are at risk for certain diseases like Alzheimer’s? And will the government or the medical establishment come between you and your genome?

One thing that is not in question is that we are moving swiftly into the personalized medicine era, and The $1,000 Genome is an essential guide to this brave new future.

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From the Author:
Although I've been writing about "the $1,000 genome" since 2002, it was two key events in 2007 that really sparked the concept for this book. The first was the presentation to Jim Watson in May of his digital genome sequence on a portable hard drive -- the first "personal genome" decoded using a new kind of DNA sequencing technology. Although the cost of Watson's genome was about $1 million, that was still a fraction of the $2.3 billion spent on the Human Genome Project.

The second was my first conversation with the co-founder of 23andMe, a pioneering consumer genomics company offering tantalizing personal genomic information at an affordable price (less than $1,000) to the public at large. Since then, tens of thousands of people have sent saliva samples to various consumer genomics firms. In a handful of cases, some recounted in the book, the results are nothing short of life-changing, and possibly life-saving.

Since 2007, the cost of genome sequencing has plummeted at an astonishing rate. Today, anyone can get their genome sequenced for less than $20,000, and that price will inevitably drop to $1,000 in the coming years as new technologies arrive. Imagine getting a full genome scan as easily and routinely as an MRI -- and without the claustrophobia! Even better, imagine a Star Trek Tricorder device reading your complete genetic code in a matter of minutes! That's a very real possibility in the next few years.

The bigger question, however, is whether that is going to make a difference to the health of yourself and your family? Having access to your full genome isn't magically going to reveal whether you're going to develop diabetes, cancer or heart disease, but it is going to become a fundamental part of your medical record. Among the challenges ahead of us discussed in the book: Will our genome data be kept private? Will we be subject to insurance or employment discrimination if we have our DNA sequenced? What can my genome really tell me about my disease risk? Who is going to explain that analysis to me -- not to mention my family doctor?

My intention in The $1,000 Genome isn't necessarily to answer all those questions, but to raise awareness of the rapidly approaching era of genome sequencing and increasingly personalized medicine. The technology will be with us very soon: the medical, legal and health care professions need to start preparing now. As should you!

See: youtube.com/watch?v=XXe74r7eYQw&feature=player_embedd
About the Author:
Kevin Davies, Ph.D., is the author of The $1,000 Genome. His previous book Cracking the Genome was translated into 15 languages. He is currently Editor-in-Chief of Bio·IT World, a trade magazine covering the role of technology in the life sciences. He was the founding editor of Nature Genetics, the world's leading genetics journal, which he headed for its first five years. He has also written for the Times (London), Boston Globe, New England Journal of Medicine, and New Scientist, among others. His first book, Breakthrough (co-authored with Michael White) told the story of the race for the BRCA1 breast cancer gene. Davies holds an M.A. in biochemistry from the University of Oxford and a Ph.D in molecular genetics from the University of London. He held postdoctoral fellowships at MIT and Harvard Medical School before moving into science publishing as an editor with Nature magazine. He lives in Lexington, Massachusetts.

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  • PublisherFree Press
  • Publication date2010
  • ISBN 10 1416569596
  • ISBN 13 9781416569596
  • BindingHardcover
  • Edition number1
  • Number of pages352
  • Rating

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