Rapid Whole-Genomic Sequencing and a Targeted Neonatal Gene Panel in Infants With a Suspected Genetic Disorder

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Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning

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Scalable, high quality, whole genome sequencing from archived, newborn, dried blood spots

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Reclassification of the Etiology of Infant Mortality With Whole-Genome Sequencing

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Artificial intelligence enables comprehensive genome interpretation and nomination of candidate diagnoses for rare genetic diseases

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