UC Santa Cruz researchers showcase how long-read sequencing can diagnose rare genetic diseases in days instead of years.
Long read sequencing revealed more genetic information in cases of 42 patients with rare diseases while cutting time and cost of diagnoses.
One in every 10 people worldwide is impacted by a rare genetic disease but about 50% of them remain undiagnosed despite rapid ...
Discover the top genomics startups revolutionizing genome sequencing technologies to enhance disease prevention and treatment ...
Key Findings Enabled by PacBio Technology: Synchronized Multiomic Sequencing: For the first time, a single sequencing run ...
The research shows that as long as essential genes remain intact, our genomes can tolerate significant structural changes, ...
As we gear towards wrapping up this exciting series, we travel to the month of April: questions are raised about the Jatiya Party, while the AL government is yet to enjoy the fruits of its victory.
How might the rise in NICs affect property investors and landlords?