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The $1,000 Genome: The Revolution in DNA Sequencing and the New Era of Personalized Medicine, by Kevin Davies
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Since the conclusion of the Human Genome Project in 2003, scientists have been racing towards a grand goal: offering individuals a decoding of their complete genetic makeup for just $1,000. As Kevin Davies reveals in this exquisitely reported account, the $1,000 genome will be a reality by 2011 and it will usher in a whole new era of personalized, genomic medicine. Capable of presenting much more advanced information than the current crop of cheek-swab services, the $1,000 complete genome raises some extraordinary possibilities. We will be able to learn if we have genes that predispose us to a host of diseases, and to take a wide range of preventative measures. Drug companies may be able to create versions of drugs tailored specifically to our individual DNA. But we may also face the psychological burden of learning that we have the gene for an incurable disease, such as Parkinson’s.
Acclaimed author Kevin Davies introduces the pioneers of this medical revolution and probes deeply into both the medical benefits and ethical issues of personal genetic testing, also exploring the psychological complexities of learning one’s DNA results, based on both his own experience of being tested and that of a number of others. The $1,000 Genome is an indispensable guide to the new era of personalized medicine.
- Sales Rank: #684146 in Books
- Published on: 2015-08-18
- Released on: 2015-08-18
- Original language: English
- Number of items: 1
- Dimensions: 8.37" h x 1.10" w x 5.50" l, .75 pounds
- Binding: Paperback
- 352 pages
Review
Once only a subject for science fiction movies, whole genome sequencing is rapidly becoming a reality for the masses. So, what does this mean for you?... Davies does a commendable job of answering that question.
--The Spittoon (spittoon.23andme.com)
Kevin Davies' The $1,000 Genome deserves to be widely read... It presents a careful and I think entertaining view of the past and possible future of personal genomics. --Keith Robison -- "Omics! Omics" (omicsomics.blogspot.com)
In this informative and accessible work of scientific journalism, Englishman Kevin Davies predicts that personalized genome sequencing will soon become so affordable that it will revolutionize medicine. --Winnipeg Free Press
``The great impact of a new technology – from cotton underwear to the jet to the computer – comes not when it is invented, but when it becomes cheap enough to be within the reach of everybody. Gene sequencing has now reached that point. With unrivalled knowledge of the people who made this possible, Kevin Davies eloquently explains how it came about, and hints at what will come next.’’ (Matt Ridley, author of The Rational Optimist)
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.
Most helpful customer reviews
7 of 7 people found the following review helpful.
reporting the real genome revolution
By Michael Gross
Back in 2000, when the draft sequence of "the" human genome was announced, hopes were high that a genetic understanding of common diseases would soon follow. This anticipated revolution in genomic medicine hasn't happened yet. However, a very different kind of revolution has happened, namely the development of fundamentally new and much more efficient methods to sequence huge amounts of DNA. As a consequence, the cost of sequencing a human genome has fallen faster than that of computer hardware. In order-of-magnitude terms, the first human genome (2000) cost around $ 1 billion, James Watson's (2007) $ 1 million, and this year many individual human genomes will be sequenced for not much more than $1000 per head.
This very real genome revolution has been underreported in the general media. Worse, it hasn't yet influenced the thinking of many medical professionals, even though it is bound to change the ways in which they will be able to prevent and treat disease. Kevin Davies, who has followed these developments closely as the editor of the magazine BioIT World and has interviewed many of the main protagonists over the years, now aims to popularise the new genome revolution in this very readable book.
Along with the progress in sequencing technology and personal genomes, Davies also covers the work of direct-to-consumer companies such as 23 and me, and also reports his own experience gained with these services. It emerges, however, that these companies are already at risk of becoming obsolete if they keep looking for simple answers from single base mutations (single nucleotide polymorphisms, or SNPs) although the large-scale view of the complexity of entire genomes is becoming more and more important.
This is a well-informed and very accessible account of the fast-moving developments that will change medical and pharmaceutical world very soon. Naturally, it will become dated very soon, so read it now.
20 of 26 people found the following review helpful.
Disappointing -
By Loyd Eskildson
I'm a biology illiterate excited by the prospects of genetic research and future genetic engineering. I was hoping that Davies' book would educate me in the basics, especially since his day job involves editing a periodical on the topic and he has a PhD in the subject. Unfortunately, Davies' book didn't do it. "The $1,000 Genome" focuses more on the key companies and leaders in the field, than explaining what's happening to neophytes. (Articles such as "The $100 Genome" in the 4/17/2008 "Technology Review" are more helpful.) As a result, the material jumps from one approach to another, and lacks a simple, structured approach. I also didn't appreciate Davies' wild numbers in some instances - eg. the U.S. spending $5 trillion on 4 million with Alzheimers.
Davies should also have devoted much more space to BGI (formerly Beijing Genomics Institute), which with its 126 new top-of-the-range sequencing machines added to an existing 31 will have supposedly more DNA-sequencing capacity than the entire U.S. Also important is what it is likely to accomplish, at least in the area of human intelligence, an area that it is focusing on. (2,000 Chinese children will have their genes sampled, and the results correlated with their test scores at school - the largest examination to date of the idea that differences between individuals' IQ scores are partly due to DNA differences.)
Nonetheless, it is impossible not to be impressed by the speed of improvement in the field - from taking 13 years and $2.7 billion to decade the first human genome , to 14 days and $1,500 by 2009. That's improvement by a factor of 10/year, far faster than even Moore's Law (doubling the number of transistors on a chip every 12-18 months). (The problem is, however, that given how Davies switches from sampling to partial DNA to entire DNA analysis, the reader is never certain whether these comparisons involve apples to apples.)
I also didn't appreciate the time Davies devoted to ethics and privacy concerns, vs. outcomes and methods.
3 of 3 people found the following review helpful.
Profiles of Some People in the Sequencing Business
By Amazon Customer
The title of this review would be an alternative suggestion for the book title.
Don't read this looking to find more about sequencing technology or uses. The book has about the technical content of a USA today article.
Here's the full description of the rise of Curagen: "He invented a patented method for studying gene expression by looking up activity patterns in a database, which he dubbed "GeneCalling". Two sentences later the company "had raised some $600 million" and it's "estimated that his major investors each made $100 million". They made money by raising money? Or does the paragraph intend to say that Curagen was *sold* for $600M? Somebody paid $600M for a method of looking up patterns in a database? Really?
This is the book for you if you want descriptions of colorful characters and what they say about each other, reporting on parties and publicity events, anecdotes about genetic defects in the relatives of people involved in the companies, ethical issues in consumer sequencing, and other such human interest flotsam.
Not for you if you'd like to learn what the technology is and what can be done with it.
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