A new study shows that long-read sequencing has the potential to improve the rate of diagnosis while reducing the time to ...

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.

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

Nanopore sequencing enables the rapid and cost-effective sequencing of entire genomes, including those of humans, animals, plants, and microorganisms. The long read lengths generated by nanopore ...

“Short-read sequencing struggles with certain kinds of sequence variants, so to better capture these, we also used long-read sequencing that reads between 5,000 and 30,000 base pairs at a time ...

Long-read sequencing enables the identification of structural variations ... Sequencing also facilitates the discovery of novel enzymes, biofuels, and biomaterials from microbial genomes. DNA ...

MENLO PARK, Calif., Jan. 14, 2025 (GLOBE NEWSWIRE) -- PacBio (NASDAQ: PACB), a leading provider of highly accurate long-read sequencing solutions, announced a significant publication from Radboud ...

However, the latest next-generation sequencing techniques are able to produce longer reads from much larger fragments of DNA nucleotide strands. There are two well-established processes for the ...

Key Findings Enabled by PacBio Technology: Synchronized Multiomic Sequencing: For the first time, a single sequencing run provided simultaneous insights into genome, methylome, epigenome, and ...