Explore how advances in accuracy, throughput and cost are making long-read sequencing more accessible at scale.

Expands access to streamlined genomic data analysis across the PacBio partner ecosystemMENLO PARK, Calif. & BERLIN, April 21, 2026 (GLOBE NEWSWIRE) -- PacBio (NASDAQ: PACB), a premier developer of ...

For years, two siblings with the distinctive facial features of Treacher Collins syndrome had no genetic explanation for ...

PacBio has announced its participation in the 1000 Genomes Long Read Sequencing Project, contributing long-read transcriptome data to enhance this significant human genomics initiative. Through ...

New extraction-to-library prep workflow enables highly accurate long-read sequencing from archived clinical samples, expanding opportunities in cancer researchMENLO PARK, Calif. and WOBURN, Mass., ...

Metagenomics relies on the use of software programs called assemblers, which can reconstruct tens of thousands of individual ...

Researchers at Rady Children’s Institute for Genomic Medicine (RCIGM) in San Diego have successfully applied long-read genome sequencing to reveal the genetic underpinnings of complex psychiatric ...

Long read sequencing improves detection of structural variants in paediatric leukaemia, identifying missed gene fusions and ...

In a way, sequencing DNA is very simple: There's a molecule, you look at it, and you write down what you find. You'd think it would be easy—and, for any one letter in the sequence, it is. The problem ...