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454’s Jonathan Rothberg believes his machines will make sequencing so cheap and fast that it will become practical to read the genomes of individuals.
Credit: Steve Moors
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A new generation of DNA-sequencing machines is opening up whole new areas of genomic research. Already, researchers are unraveling how modern humans differ from Neanderthals and devising more precise tests for cancer.
On February 6, 2007, executives from 454 Life Sciences showed 78-year-old James Watson a first draft of his own genome. There was something downright poetic about this. Watson, of course, had won a Nobel Prize 45 years earlier for his role in discovering the double-helical structure of DNA; he was also a prime mover behind the Human Genome Project, which by its completion in 2003 had spent nearly $3 billion over 13 years extracting the blueprint that those helices encode. Now 454 had moved a step beyond that megaproject, which pooled many people's DNA to determine the genetic sequence of what amounts to a model human. The company and its so-called next-generation sequencing machine had single-handedly read the genetic code of an individual--one whose work had done so much to make the achievement possible.
But Jonathan Rothberg, who founded 454 in Branford, CT, with the dream of producing a sequencing machine more efficient than those available to the Human Genome Project, does not mention poetry when he recounts his meeting with Watson. Rather, he talks about money, speed, and a future in which ordinary people carry around their personal genomes on discs--an increasingly plausible scenario. "It cost us $200,000 to do Jim Watson," points out Rothberg. "And we did it mostly in December and January."
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