$280 Million Boost for Disease Genomics

The genomics arm of the National Institutes of Health has pledged a total of $280 million for research into the genetic bases of disease.

Written byCatherine Offord
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NIH Building 1WIKIMEDIA, NATIONAL CANCER INSTITUTEThe National Human Genome Research Institute (NHGRI) announced in a press release last week (January 14) that it will provide more than $240 million over the next four years to fund research into the genomic variation underlying common diseases.

“The time is right for a very large-scale human genome sequencing program” in order to understand, “the genetic and environmental causes of common diseases,” NHGRI Director Eric Green told reporters (via STAT News). “The kind of information that can come out of this is overwhelmingly medically important.”

To spearhead the project, NHGRI has launched the Centers for Common Disease Genomics (CCDG), which will focus on diseases including diabetes, autism, and heart disease. Researchers at four funded centers associated with universities and colleges across the U.S. will sequence tens of thousands of genomes from individuals with and without the diseases in order to identify underlying genomic causes and correlations. The National Heart, Lung, and Blood Institute will provide an additional $20 million for the CCDG centers, ...

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Meet the Author

  • After undergraduate research with spiders at the University of Oxford and graduate research with ants at Princeton University, Catherine left arthropods and academia to become a science journalist. She has worked in various guises at The Scientist since 2016. As Senior Editor, she wrote articles for the online and print publications, and edited the magazine’s Notebook, Careers, and Bio Business sections. She reports on subjects ranging from cellular and molecular biology to research misconduct and science policy. Find more of her work at her website.

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