Monthly Archives: February 2015

Highlights from the Network, February 2015

Through our collaborations and programs like the GET Conference, Personal Genome Project, & Open Humans, we have the good fortune of interacting with a lot of people doing incredible things in the world.  So we are continuing with our series that will keep track of noteworthy articles and media featuring individuals in our broad network.  Here is a selection of recent highlights. We hope you enjoy it:

 

What We’re Reading

A list of things from around the web that we’re reading. Hope you enjoy!

Who Should Have Access to Your DNA? Medium

UW Study Finds Returning Incidental Findings May be Cost Effective. Genome Web

Topol: Why Are Doctors and Hospitals the Owners of Patient Records? Medscape

Teen identifies rare mutation in her own cancer, champions new age of open-access genetics. Genetic Literacy Project

Biology, Computing, and the History of Molecular Sequencing: From Proteins to DNA, 1945–2000.

Discrimination based on genetics could soon be illegal, and it’s right on time. Canada.com

The First Amendment Right to Speak about the Human Genome. Social Science Research Network

Trust me, I’m a medical researcher. Science Magazine

Every Patient a Subject: When personalized medicine, genomic research, and privacy collide. Slate

Small company offering direct-to-consumer whole genomes for just $1850 Facebook post (related to the New product for 2015: sub-$2000 whole-genome sequencing announcement from Full Genomes).

Highlights from the Network, December 2014 and January 2015

Through our collaborations and programs like the GET Conference, Personal Genome Project, & Open Humans, we have the good fortune of interacting with a lot of people doing incredible things in the world.  So, we are starting a new series that will keep track of noteworthy articles and media featuring individuals in our broad network.  Here is a selection of recent highlights, we hope you enjoy it: