1. We could do much more thorough sampling of other environments. For example, we could sample wind traps, balloons, or seawater. This would provide much more granular information about how pathogens (or any microscopic organisms) move through the environment.
2. In general we should expect every person to know their complete DNA sequence. It should not be very difficult to continuously update a risk tracker for conditions and infections as new research becomes available, allowing automatically up-to-date personalized medicine.
3. Since we can keep re-sequencing DNA, we should be able to test for epigenetic effects much more thoroughly.
1. We could do much more thorough sampling of other environments. For example, we could sample wind traps, balloons, or seawater. This would provide much more granular information about how pathogens (or any microscopic organisms) move through the environment.
2. In general we should expect every person to know their complete DNA sequence. It should not be very difficult to continuously update a risk tracker for conditions and infections as new research becomes available, allowing automatically up-to-date personalized medicine.
3. Since we can keep re-sequencing DNA, we should be able to test for epigenetic effects much more thoroughly.