Scientists have turned traditional genomics research on its head. Instead of trying to find a mutation in the genome of a person with a genetic disease, they sequenced the genomes of healthy participants, and then analyzed the data to find presumed mutations that would almost certainly lead to a genetic condition. Of nearly 1,000 volunteers whose genomes were examined, about 100 had variants predicting a rare disease. Almost half actually had the disease.
from Today's Healthcare News -- ScienceDaily http://ift.tt/1BPvkC9
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