A UK program will sequence the genomes of 100,000 newborn babies | CNN
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Illumina, Chinese Children's Hospital to Launch Newborn Sequencing Study | GenomeWeb
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Brotman Baty Institute Collaborates with Illumina and GeneDx on Whole-Genome Sequencing Study to Support Families of Children with Developmental Differences | Brotman Baty Institute
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Illumina, Inc. - What is "Project Baby Bear," and how is it working to demonstrate the financial and clinical benefits from improved and accelerated access to clinical whole genome sequencing? Learn more
NGS Identifies Rare Disease Variants in Infants with Undiagnosed Disease
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Illumina Joins Children's Hospital of Fudan University to Study Rapid WGS in NICU | Inside Precision Medicine