March 28, 2022 | by BBI Communications
Initial results of the BBI-sponsored SeqFirst Project using whole genome sequencing have demonstrated that “clear opportunities exist to center equity for providing a precise genetic diagnosis that adds value to the care of critically ill newborns.”
Read MoreJanuary 24, 2022 | by BBI Communications
‘It’s one thing to find a genetic variant. But how does that affect the brain architecture, structure, and function? We wanted to know more.’
Read MoreMay 26, 2021 | by BBI Communications
On May 19, The Brotman Baty Institute and Seattle Children’s co-hosted a one-day Pediatric Sequencing Symposium. Sessions ranged from the genomics of pediatric epilepsy disorders, to extended family outreach after finding hereditary cancer risk.
Read MoreApril 28, 2021 | by BBI Communications
The project, SeqFirst, will provide early access to whole-genome sequencing (WGS) to 100 children suspected of having developmental differences at the point of diagnosis.
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