Browse an up-to-date collection of news from the major scientific and media publishers. Click on the news to be immediately redirected to the original source. Please contact us about any other relevant news.
Is it safe to give your genetic data to 23andMe? CEO Anne Wojcicki explains the DNA testing company’s privacy protections on the latest Too Embarrassed to Ask.
22 Septembre 2017, Recode
Stanford researchers used cryptography to cloak irrelevant genetic information in individuals’ genomes while revealing disease-associated mutations. They say the technique could vastly improve patient privacy.
17 August 2017, Stanford Medicine News Center
It is now possible to scour complete human genomes for the presence of disease-associated genes without revealing any genetic… Read more >>>
22 June 2017, The Irish Times
Speaking at the inaugural Data Summit in Dublin organised by the Department of the Taoiseach, Ms Dixon outlined the challenges to privacy from the so-called digital revolution, but also the opportunities… Read more >>>
6 June 2017, Huffington Post
“One family asked me: ‘Will they be able to clone my baby?’”
That’s not a typical question, says genetic counselor Shawn Fayer, just an anecdote. Still, it fits a theme. For parents considering whether to have their newborn’s genome sequenced as part of the BabySeq Project, genetic privacy and discrimination… Read more >>>
In the United States in 2015, the number one target for cyber-attackers was health data. While that number is shrinking thanks to efforts by the security and privacy research community, health data are still a very common target of cyber-attacks.
7 April 2017, GA4GH News
In a paper recently published in the Journal of the American Medical Information Association, Baker and a team of GA4GH volunteers led by genomics security expert Jean-Pierre Hubaux put forth three new strategies for mitigating the risks of cyber attacks on Beacon datasets….Read more >>>
PharmaTimes magazine – April 2017
To gain access to this data, the public may have to be willing to share their own genetic information – but is this something they want?…Read more >>>
Personalized medicine promises much. New initiatives aim to harness technology and genomics to create bespoke medicine, customizing your healthcare like your Facebook profile. Instead of relying on generic practice guidelines, your doctors may one day use these new analytic tools to find the ideal treatment for you.
26 March 2017, Oxford University Press
But this precision has a price that science and medicine don’t acknowledge. Personalized medicine demands that we all contribute our medical histories and genomes to the big data research pool. The science works only if the numbers are very large; so large that some envision every patient as a subject whose medical data will be shared for research. As this future unfolds, you will, of course, be assured of your privacy. Unfortunately, that’s a promise science cannot honestly make and you should not believe….Read more >>>
22 November 2016, MIT Technology Review
In August 2015, Samantha Schilit went to her primary care doctor to get a blood draw. A PhD candidate at Harvard specializing in human genetics, she was itching to unlock the secrets of her genes with a test called whole-genome sequencing, which provides a full readout of a person’s DNA…Read more >>>
13 September 2016, Undark
WHEN PRESIDENT BARACK OBAMA hosted a summit earlier this year on his research initiative to gather DNA samples and medical histories on a million volunteers, he highlighted the delicate balance between science and privacy inherent in genomic information…Read more >>>
20 August 2016, Trendintech
But, because there is a significant amount of personal data stored on one single database it poses high-security risks that people’s medical histories may be accessed for the wrong reasons. However, researchers from MIT’s Computer Science and Artificial Intelligence Laboratory and Indiana University at Bloomington have recently disclosed…Read more >>>