Read the article in full.
From the Telegraph Genomics are not overhyped: they really can change medicine
It is correct that science has not made as much progress as had been hoped in unlocking the genetic factors that contribute to most common diseases. But quite staggering progress has been made elsewhere. In three areas in particular cancer, rare congenital diseases and infections the plummeting cost of reading DNA and sciences growing ability to interpret it is already transforming medical practice. The Genomics England project is about bringing these benefits to NHS patients, and enabling further scientific discoveries to emerge from their care.
Read the article in full.
From the Guardian What we can all gain from personal genetics
Learning about your genetics enables you to optimize your health. It will take us decades to understand all 3bn base pairs in the human genome, but today we already know what thousands of important genetic differences mean for individuals.
We know that genes affect your risk for conditions like cystic fibrosis and breast cancer, and we know how your genes affect your responses to drugs like Warfarin. As genetic testing becomes more affordable, more people can benefit from understanding their genetics and use that understanding to improve their health, help them prevent the harmful side-effects of some drugs and potentially avoid preventable deaths.
For example, roughly 8 per cent of people with European ancestry have a genetic variant that puts them at higher than average risk for blood clots. There are a number of easy ways to minimize this risk, ranging from avoiding oral contraceptives to staying hydrated and maintaining mobility during airplane flights.
Read the article in full.
From Huffingon Post Personal Genomics for All
The rest is here:
Genomics: what it could mean for the future of medicine