A Quote by Peter Singer
If we can put a man on the moon and sequence the human genome, we should be able to devise something close to a universal digital public library.
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The question is, are there useful things that we can do with the results of a genome sequence that would bring benefit? And the answer is, today, should the majority of people go and have their genome sequenced? Probably not. But are there particular circumstances in which genome sequencing is really helpful? Yes, there are.
Eventually we'll be able to sequence the human genome and replicate how nature did intelligence in a carbon-based system.
As a Christian, but also as a scientist responsible for overseeing the Human Genome Project, one of my concerns has been the limits on applications of our understanding of the genome. Should there be limits? I think there should. I think the public has expressed their concern about ways this information might be misused.
[Decoding the human genome sequence] is the most significant undertaking that we have mounted so far in an organized way in all of science. I believe that reading our blueprints, cataloguing our own instruction book, will be judged by history as more significant than even splitting the atom or going to the moon.
The first thing you have to do is to sequence the Neanderthal genome, and that has actually been done. The next step would be to chop this genome up into, say, 10,000 chunks and then... assemble all the chunks in a human stem cell, which would enable you to finally create a Neanderthal clone.
The fact is that proprietary databases don't work for such basic and broadly needed information as the sequence of the human genome.
Ours is not a dumb species. We have put a man on the moon. We have unlocked the secrets of the human genome. We have discovered how to take stem cells and coax them into becoming brain cells, heart muscle, liver tissue - any organ of the human body that needs repair. These are our miracles, and there are more. Yet we have not yet found a way to do the simplest things: To live in peace. To stop killing each other when we disagree. To distribute that which is good in life freely and fairly.
There's always a question when you invest. Are you too early, are you too late, or are you just right? And there was a lot of hype about life sciences, around the sequencing of the human genome and a lot of people concluded that's not really there. But by the way, there was a lot of hype around the digital revolution just about the time of 2000 and the human genome, and it turns out that some of the world's biggest, most powerful companies are the survivors post that crash.
How did we cure polio, smallpox and send a man to the moon? How did we decode the human genome in just 13 years? Collaboration. Focus on a specific goal, and teamwork.
The convergence of information technology and biology allows scientists to translate the human genome into digital data that can accelerate diagnoses and cures.
We share half our genes with the banana. [After the announcement Jun 2000 that a working draft of the genetic sequence of humans had been completed by the Human Genome Project.]
The day is not far off when we will be able to send a robotically controlled genome-sequencing unit in a probe to other planets to read the DNA sequence of any alien microbe life that may be there.
I was so inspired by Dr. King that in 1956 with my brothers and sisters and first cousins, I was only 16 years old, we went down to the public library trying to check out some books and we were told by the librarian that the library was for whites only and not for colors! It was a public library! I never went back to that public library until July 5th, 1998, by this time I'm in the Congress, for a book signing of my book "Walking with the Wind"
The mouse genome is an invaluable tool to interpret the human genome.
Three billion bases of DNA sequence can be put on a single compact disc and one will be able to pull a CD out of one's pocket and say, 'Here is a human being; it's me!'
If I could get every single cancer genome sequence that has been sequenced; if I could ever put it in one repository, we have the capacity to do a million billion calculations per second. We'll be able to find out more in 10 minutes more than it would take 10 Nobel laureates 10 years to find out about the patterns of cancer and the cures for cancer.
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