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GeneDx has sequenced over three quarters of a million exomes/genomes. Their clinical results have demonstrated that exome/genome sequencing delivers higher diagnostic yield than traditional methods such as chromosomal microarray or multigene panels. Rapid whole genome sequencing can identify genetic causes in critically ill infants within as little as two days. The GUARDIAN study led by GeneDx has shown the value of genomic newborn screening at scale to detect actionable conditions missed by standard protocols.
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