Long-Read Sequencing Transforms Rare Disease Diagnosis with Breakthrough Precision
Revolutionizing Rare Disease Diagnosis: The promise of Long-Read Sequencing One in every 10 people worldwide is affected by a rare genetic disease, yet about 50% of these cases remain undiagnosed despite advancements in genetic technology. For those who do have access to testing, the journey to a diagnosis can take five years or more—often too … Read more
