New method taps family trees for clues about conditions – Spectrum

Genetic puzzle: A new approach for finding risk variants considers data from multiple generations of a family. Hero Images/Getty Images

Asking participants in genetic databases about their family’s medical history can help researchers uncover genetic variants tied to uncommon conditions. Because people share 50 percent of their DNA with each of their parents, siblings and children, the DNA of the participants holds clues to the conditions of these relatives.

Read the full story in Spectrum.

Advertisements

Spiking genomic databases with misinformation could protect patient privacy – Nature

Nature

Large genomic databases are indispensable for scientists looking for genetic variations associated with diseases. But they come with privacy risks for people who contribute their DNA. To address those concerns, a system developed by Bonnie Berger and Sean Simmons, computer scientists at MIT, masks the donor’s identity by adding a small amount of noise, or random variation, to the results it returns on a user’s query.