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.

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A fire at a Manchester hospital may have destroyed lab equipment and data, the Guardian reports.

Researchers generate a genetic database from skeletal remains from the 1845 Franklin Expedition to the Arctic, Live Science reports.

Researchers in China have begun another trial using CRISPR/Cas9 approaches in cancer patients, according to the Wall Street Journal.

In Science this week: human DNA found in sediments from archeological sites lacking bones, and more.

May
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This webinar is the last in a four-part series highlighting real-world examples of how some lab directors are bringing validated next-generation sequencing-based tests to the clinic.