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December 18, 2013

Fragile Expedition

SMRT Sequencing technology is helping provide insight into FragileX syndrome, a research area that Dr. Paul Hagerman at the UC Davis School of Medicine has passionately been working to develop a diagnostic test for in the future.


December 2, 2013

Seeing the Whole Elephant

Short sequencing reads obtained by RNA-seq offer precise counts of expressed transcripts, but no information on their structures. Now, researchers report a new approach using circular cDNA templates and PacBio long sequencing reads that enables quantitation of transcript isoforms.


May 6, 2013

Finishing Genomes with HGAP

Scientists from DOE JGI, PacBio and UW collaborate to develop a fully automated process from DNA sample preparation to the determination of the finished genome.


April 3, 2013

Going to Great Read Lengths

In a revival of the era of finished genomes, scientists are using the long reads offered by sequencing technologies to close gaps in genome assemblies.


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