– Genomic Diagnosis of Rare Pediatric Disease in the United Kingdom and Ireland
– Diagnostics for rare diseases
– Automated prioritization of sick newborns for whole genome sequencing using clinical natural language processing and machine learning
– Genetic association analysis of 77,539 genomes reveals rare disease etiologies
Diagnóstico genómico de enfermedades raras
Filed under Algoritmos, Diagnóstico, Genómica, Medicina personalizada, Polimorfismos by on . 
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