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Whole genome testing, which is twice as effective at detecting genetic diseases than targeted tests, saved one infant with a rare, deadly condition. Experts say it could save millions more lives in the future.
A “whole genome” genetic test is nearly twice as good as a narrower test at unearthing genetic abnormalities, according to research.
Brynn Schulte nearly died twice when she was a baby, at one point needing emergency surgery for massive bleeding in her brain.
Last year Europe witnessed its worst dry spell in 500 years in which ships carried only a fraction of the cargo they usually do along Germany's Rhine river.
A recent study published in the Journal of the American Medical Association found that "whole genome" tests are twice as effective as narrower tests in identifying genetic abnormalities that can cause disease in infants.