Scientists know that a map of our genome holds boundless potential, ranging from identifying our susceptibility to disease to discovering cures for cancer. But since 1953, when James Watson and Francis Crick concluded that DNA contained the "stuff of life," only a handful of human genomes have been mapped. In fact, it still takes many months and millions of dollars to sequence a single genome.
Understanding our genomes may help delay or even prevent disease. For those suffering from genetic illnesses, personal genetic information can determine which medicines will drive their disease into remission without negative side-effects.
The Archon X PRIZE for Genomics challenges scientists and engineers to create better, cheaper and faster ways to sequence genomes. The knowledge gained by compiling and comparing a library of human genomes will create a new era of preventive and personalized medicine — and transform medical care from reactive to proactive.
The X PRIZE Foundation and scientists the world over dream of the day when we fully understand the human genetic blueprint — enabling us to make informed decisions about our own health and create a brighter future for generations to come.
Please join the X PRIZE Foundation in our challenge to create a breakthrough in genomics that will benefit all of humanity.
