Explore how advances in accuracy, throughput and cost are making long-read sequencing more accessible at scale.
Long read sequencing improves detection of structural variants in paediatric leukaemia, identifying missed gene fusions and ...
MENLO PARK, Calif., Feb. 12, 2026 (GLOBE NEWSWIRE) -- PacBio (PACB), a leading provider of high-quality, long-read sequencing technologies, today announced a collaboration with iHope, a global rare ...
Powered by GeneDx Infinity™ with unparalleled scale and diversity, GeneDx fuels breakthrough scientific research and delivers the most precise rare disease diagnosis for patients and families “GeneDx ...
The National Institute on Aging’s Long Life Family Study (LLFS) selected PacBio technology to generate genomic and epigenomic data from as many as 7,800 participants. The effort will rely on PacBio’s ...
The single-cell genomics industry does not stop advancing, with a steady stream of new companies, kits, acquisitions, and more. One new company, ArgenTag, was founded in Argentina during the COVID-19 ...
To celebrate its addition to PacBio’s (CA, USA) Compatible Partner Program, ArgenTag (NY, USA) has announced the opening of a grant program to provide access to single-cell sequencing tech, free of ...
Oxford Nanopore long-read sequencing helps researchers derive insights from difficult-to-read genomic sections and detect large structural variants. However, the technique uses high molecular weight ...
Saliva can provide researchers with a source of high-quality human genomic DNA. Although blood is commonly employed for this purpose, saliva offers several advantages. It is more readily accessible, ...
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