“However, typical single-cell sequencing experiments use what ... so to better capture these, we also used long-read sequencing that reads between 5,000 and 30,000 base pairs at a time and ...

One in every 10 people worldwide is impacted by a rare genetic disease but about 50% of them remain undiagnosed despite rapid ...

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.

New AI model takes minutes rather than days to predict how a specific DNA sequence will arrange itself in the cell nucleus.

Ph.D. student Shloka Negi analyzes long-read sequencing data in the UC Santa Cruz Computational Genomics lab.

There are two well-established processes for the delivery of long-read sequencing. The first, nanopore sequencing ... The latest developments involve single-cell sequencing to provide more accurate ...

Using a single-cell sequencing technique, it was possible to characterize the different cell types present in the brain ...