CHICAGO (GenomeWeb) – Genome.One, an Australian startup offering clinical whole-genome sequencing services to help diagnose rare genetic conditions, will work with Sanford Health to develop a platform to incorporate patient-generated health data into WGS data, the companies announced yesterday.

The two organizations are aiming to combine data provided by Sanford patients with information in electronic health records and genetic and research knowledge bases. This, according to Sanford Health, offers promise for diagnosis and treatment of rare diseases.

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