Whole-genome sequencing can be used to identify patients' risk for hereditary cancer, researchers have demonstrated. This is the first study that has used whole-genome sequencing to evaluate a series of 258 cancer patients' genomes to improve the ability to diagnose cancer-predisposing mutations, researchers say.
from Today's Healthcare News -- ScienceDaily http://ift.tt/1zwRe00
from Today's Healthcare News -- ScienceDaily http://ift.tt/1zwRe00
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