Newborn Screening for Rare Diseases by 4 Power Biomarkers WGS-HiFi Test

28 March in genome resequencing, PacBio Sequencing

Unlocking Early Detection: How Whole Genome Sequencing (WGS) with HiFi Technology is Revolutionizing Newborn Screening for Rare Diseases Newborn screening (NBS) has long been a cornerstone of preventive healthcare, saving countless lives by identifying treatable conditions before symptoms appear. Traditional NBS relies on biochemical tests from...

Rare Disease Hackathon India 2026

27 February in Uncategorized

Undiagnosed Hackathon India 2026 Brings Global Experts Together to End the Diagnostic Odyssey for Rare Disease Families Hyderabad, Feb 2026—The Undiagnosed Hackathon India 2026 convened clinicians, genomic scientists, data analysts, and patient advocates from across the world with a single mission: to help families whose children...