Up until now we have mainly used only one human genome as a reference, when sequencing and analyzing a person's genome.
This is about to change. A new version of the human genome map called "pangenome" will include genomes from a wide diversity of people to create a genetic atlas that better captures the genetic diversity of our species.
This is an important step towards understanding our DNA and genetic differences, and to better diagnose rare diseases and develop cures using the latest developments in gene therapy.
In 2001, the cost of full genome sequencing was around $ 100M and took 9 months - today the cost is around $ 200 and can be done in a few hours. This means we are seeing an explosion in the number of genomes sequenced.
Combine that data with biometric data from wearable devices and new sensor technology - and throw in the latest exponential progress in artificial intelligence and computing into the mix.
We are now seeing the very beginning of a genomic revolution that will fundamentally reshape healthcare and our ability to understand how our DNA shapes us.
Up until now we have mainly used only one human genome as a reference, when sequencing and analyzing a person's genome. This is about to change. A new version...