At the Conversation, the University of Oxford's Michael Macklay writes that learning genetic risk of disease is a personal decision.
The analysis also traced the origins of the retroviruses to the ancient ocean and found that they broadly diverged alongside their hosts.
The grant, made through Innovate UK, will specifically fund a collaboration between Oxford Genetics and researchers at the University of Oxford.
The test is based on MDNA's Mitomic technology, which enables the isolation of mitochondrial DNA in circulation that may be used as biomarkers.
Genomics plc will analyze de-identified genomics data for the consortium to inform pharmaceutical research and development investment decisions.
Living DNA can break down the origins of a customer’s ancestry into 21 distinct regions within Britain alone, as well as across 80 different worldwide populations.
Researchers uncovered 60 genomic loci associated with birth weight and found that those regions are also linked to risk for type 2 diabetes and other diseases.
The Albert and Mary Lasker Foundation has announced this year's recipients of its prizes honoring basic and clinical research.
Using genome sequence data from almost 65,000 individuals, researchers identified 39.2 million SNPs that can be applied to improved genotyping imputation.
The partnership is part of a broader agreement between Genome BC and Genomics England to share data and tools around cancer and rare and infectious diseases.
In Science this week: genetic target for urothelial bladder cancer treatment, and more.
Two dozen scientific organizations have endorsed the March for Science, according to ScienceInsider.
Researchers in Japan describe a chimpanzee with a chromosomal abnormality similar to human Down syndrome, Mashable reports.