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.
15 August 2016, Nature News
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. A 2013 study1 showed that hackers could use publicly available information on the Internet to identify people from their anonymized genomic data…Read more >>>
19 March 2016, GenomeWeb
The patients — Barbara Zeughauser, Ken Deutsch, Runi Limary, and AnneMarie Ciccarella — received genetic testing from Myriad to assess their risk for cancer. In February, asserting their rights under the Health Insurance Portability and Accountability Act (HIPAA) Privacy Rule, they requested access to all genetic variants identified during testing….Read more >>>
Four new grants from the National Institutes of Health will support research on the ethical, legal and social questions raised by advances in genomics research and the increasing availability of genomic information.
17 May 2016, National Institutes of Health
The awards will fund researchers at interdisciplinary centers through the National Human Genome Research Institute’s (NHGRI) Centers of Excellence in Ethical, Legal and Social Implications Research (CEER) program. The projects will examine the use of genomic information in the prevention…Read more >>>
Researchers at Vanderbilt University School of Medicine have received a four-year, $4-million grant from the National Institutes of Health to establish a new center for the study of privacy concerns associated with the use of genomic information, the NIH announced today, May 17.
17 May 2016, EurekAlert
The Vanderbilt Center for Genetic Privacy and Identity in Community Settings will examine the likelihood that lapses in protecting genomic information allow people to be identified, how people perceive such risks, and how effective legal and policy efforts are in reducing them…Read more >>>
The American Society of Human Genetics said this week that it opposes recent revised regulations by the US Equal Employment Opportunity Commission (EEOC) that affect the American with Disabilities Act (ADA) and the Genetic Information Nondiscrimination Act (GINA).
17 May 2016, GenomeWeb
EEOC proposed the changes, which apply to employer-backed wellness programs, last year and provided stakeholders with an opportunity to comment by the end of January. A number of advocacy groups and stakeholders objected to the proposal, arguing that it would weaken genetic anti-discrimination protection…Read more >>>
According to the latest report published by Credence Research, Inc. “Direct-to-Consumer Genetic Testing: Market Growth, Future Prospects and Competitive Analysis, 2016-2022,” the direct-to-consumer genetic testing market was valued at USD 70.2 Mn in 2015, and is expected to reach USD 340 Mn by 2022, expanding at a CAGR of 25.1% from 2016 to 2022.
10 May 2016, Mobile Computing Today
Conventionally, genetic tests have been made available only through healthcare providers at recommendations from physicians . Direct-to-consumer (DTC) genetic testing is defined as genetic teats marketed directly to individuals through agencies such as internet, pharmacies and others. DTC genetic testing market is predominantly driven by growing awareness in public about…Read more >>>
In an open-access pilot project, researchers from Baylor College of Medicine have demonstrated that cancer patients are willing and able to provide “true informed consent” for sharing their genome sequencing data.
1 March 2016, GenomeWeb
They hope that open datasets of “real world” cases will be useful for advancing precision cancer treatment and spur public discussion about protecting patients’ privacy while respecting their autonomy to share data freely to advance science. According to researchers led by Baylor’s Lauren Becnel and Richard Gibbs, the pilot project, in which seven patients agreed to openly share data from sequencing their tumor and matched normal samples, is the first of its kind in the cancer setting…Read more >>>
7 April 2016, GenomeWeb
The Genetic Research Privacy Protection Act (S.2744), introduced by Senators Elizabeth Warren (D-MA) and Mike Enzi (R-WY) to the Committee on Health, Education, Labor, and Pensions, would ensure that researchers conducting federally funded studies cannot reveal genetic information that can identify individuals who donated their data. Yesterday, during a session of the HELP committee, legislators voted to attach S.2744 as an amendment to Senator Lamar Alexander’s (R-Tenn.) “Advancing Precision Medicine Act of 2016.”…Read more >>>
25 February 2016, Nature methods
The rapid emergence of cost-effective genomic sequencing is providing unprecedented insight into the genetic variation between individuals. Driven by initiatives in precision medicine, researchers are increasingly focused on understanding the relationships among genetic variations, human disease and clinical outcome…Read more >>>
Sure Genomics, a startup based in Utah, launched a genetic testing service today that costs a whopping $2,500 upfront, with an additional $150 subscription fee that guarantees DNA analysis updates every six months.
9 February 2016, The Verge
The price is unusually high for a direct-to-consumer genetics company, since 23andMe and Ancestry offer genetics reports for $199 and $99, respectively. But Sure Genomics says it’s worth it; customers who pay the fee will get their entire genome sequenced, and unlike others, the startup says it won’t sell anonymized genetic information to third parties to turn a profit…Read more >>>