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Study Shows Fabric’s GEM AI Improves Rare Disease Diagnosis

Genomics News

Fabric Genomics and Rady Children’s Institute for Genomic Medicine today announced the publication of a retrospective study in Genome Medicine showing that Fabric’s GEM AI algorithm helped detect more than 90% of disease-causing variants in infants with rare diseases. The study involved six leading genomic centers and hospitals, and used whole-genome and whole-exome data from previously diagnosed newborns and rare disease patients at Rady Children’s Hospital and the other sites.

Study Shows Fabric’s GEM AI Improves Rare Disease Diagnosis

 

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