The largest population genome sequencing effort to date is published today in Nature. Based on data collected by the UK10K project, the study was designed to explore the contribution of rare genetic variants to human disease and its impact on risk factors. Rare genetic variants are changes in DNA that are carried only by relatively few people in a population.

Classified as: McGill, celia greenwood, mcgill faculty of medicine, Lady Davis Institute (LDI), Brent Richards, UK10K, genome project, human genome, rare genetic variants, bioinfomatics
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Published on: 15 Sep 2015
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