May 2007
Sequencing in a Flash
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.
By Jon Cohen
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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 |
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.
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