Scientists have utilized a machine-learning process and clinical natural language processing (CNLP) to diagnose rare genetic diseases in record time. This new method is speeding answers to physicians caring for infants in intensive care and opening the door to increased use of genome sequencing as a first-line diagnostic test for babies with cryptic conditions.
from Top Technology News -- ScienceDaily http://bit.ly/2IGYyBA
Thursday, April 25, 2019
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