NEW YORK (GenomeWeb News) – Four European research teams will use €38 million ($50.8 million) in funding from the European Union to harness genomic knowledge in developing new diagnostics and treatments for a range of rare diseases, Newcastle University said today.

Four new research programs were launched today by the International Rare Diseases Consortium (IRDiRC) that aim to use epigenetic, genetic, and whole-genome sequencing data to fuel development of these new applications.

To read the full story....

Register for Free.

Already have a GenomeWeb or 360Dx account?
Login Now.

The New York City medical examiner is overseeing an effort to identify missing persons using DNA, according to the Associated Press.

Nobel laureate Günter Blobel has died at 81, the New York Times reports.

In PNAS this week: mouse model of genetically induced emphysema, gene expression signatures of circulating melanoma cells, and more.

Technology Review reports that 2017 was the year of consumer genetic testing and that it could spur new analysis companies.