How digital DNA could help you make better health choices
What if you could know exactly how food or medication would impact your health -- before you put it in your body? Genomics researcher Jun Wang is working to develop digital doppelgangers for real people; they start with genetic code, but they'll also factor in other kinds of data as well, from food intake to sleep to data collected by a "smart toilet." With all of this valuable information, Wang hopes to create an engine that will change the way we think about health, both on an individual level and as a collective.

1,334,433 views April 2017~~July 2022 | Jun Wang • TED

Jun Wang
Genomics researcher
At iCarbonX, Jun Wang aims to establish a big data platform for health management.
Today I'm here, actually, to pose you a question. What is life? It has been really puzzling me for more than 25 years, and will probably continue doing so for the next 25 years. This is the thesis I did when I was still in undergraduate school. While my colleagues still treated computers as big calculators, I started to teach computers to learn. I built digital lady beetles and tried to learn from real lady beetles, just to do one thing: search for food. And after very simple neural network -- genetic algorithms and so on -- look at the pattern. They're almost identical to real life. A very striking learning experience for a twenty-year-old.
00:55
Life is a learning program. When you look at all of this wonderful world, every species has its own learning program. The learning program is genome, and the code of that program is DNA. The different genomes of each species represent different survival strategies. They represent hundreds of millions of years of evolution. The interaction between every species' ancestor and the environment.
01:34
I was really fascinated about the world, about the DNA, about, you know, the language of life, the program of learning. So I decided to co-found the institute to read them. I read many of them. We probably read more than half of the prior animal genomes in the world. I mean, up to date.
01:57
We did learn a lot. We did sequence, also, one species many, many times ... human genome. We sequenced the first Asian. I sequenced it myself many, many times, just to take advantage of that platform. Look at all those repeating base pairs: ATCG. You don't understand anything there. But look at that one base pair. Those five letters, the AGGAA. These five SNPs represent a very specific haplotype in the Tibetan population around the gene called EPAS1. That gene has been proved -- it's highly selective -- it's the most significant signature of positive selection of Tibetans for the higher altitude adaptation. You know what? These five SNPs were the result of integration of Denisovans, or Denisovan-like individuals into humans.
02:52
This is the reason why we need to read those genomes. To understand history, to understand what kind of learning process the genome has been through for the millions of years. By reading a genome, it can give you a lot of information -- tells you the bugs in the genome -- I mean, birth defects, monogenetic disorders. Reading a drop of blood could tell you why you got a fever, or it tells you which medicine and dosage needs to be used when you're sick, especially for cancer.
03:23
A lot of things could be studied, but look at that: 30 years ago, we were still poor in China. Only .67 percent of the Chinese adult population had diabetes. Look at now: 11 percent. Genetics cannot change over 30 years -- only one generation. It must be something different. Diet? The environment? Lifestyle? Even identical twins could develop totally differently. It could be one becomes very obese, the other is not. One develops a cancer and the other does not. Not mentioning living in a very stressed environment.
04:07
I moved to Shenzhen 1