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The Genome Odyssey: Medical Mysteries and the Incredible Quest to Solve Them
Price $28.99Hardcover
In Stock
Euan Angus Ashley
Harvard Book Store's virtual event series, the Harvard University Division of Science, and the Harvard Library welcome EUAN ANGUS ASHLEY—professor of Medicine and Genetics at Stanford University—for a discussion of his latest book, The Genome Odyssey: Medical Mysteries and the Incredible Quest to Solve Them. He will be joined in conversation by SIDDHARTHA MUKHERJEE, pioneering physician and author of the Pulitzer Prize–winning book, The Emperor of All Maladies: A Biography of Cancer.
Since the Human Genome Project was completed in 2003, the price of genome sequencing has dropped at a staggering rate. It’s as if the price of a Ferrari went from $350,000 to a mere forty cents. Through breakthroughs made by Dr. Ashley’s team at Stanford and other dedicated groups around the world, analyzing the human genome has decreased from a heroic multibillion dollar effort to a single clinical test costing less than $1,000.
For the first time we have within our grasp the ability to predict our genetic future, to diagnose and prevent disease before it begins, and to decode what it really means to be human.
In The Genome Odyssey, Dr. Ashley details the medicine behind genome sequencing with clarity and accessibility. More than that, with passion for his subject and compassion for his patients, he introduces readers to the dynamic group of researchers and doctor detectives who hunt for answers, and to the pioneering patients who open up their lives to the medical community during their search for diagnoses and cures.
He describes how he led the team that was the first to analyze and interpret a complete human genome, how they broke genome speed records to diagnose and treat a newborn baby girl whose heart stopped five times on the first day of her life, and how they found a boy with tumors growing inside his heart and traced the cause to a missing piece of his genome.
These patients inspire Dr. Ashley and his team as they work to expand the boundaries of our medical capabilities and to envision a future where genome sequencing is available for all, where medicine can be tailored to treat specific diseases and to decode pathogens like viruses at the genomic level, and where our medical system as we know it has been completely revolutionized.
