Last week, Pacific Biosciences entered into an agreement with Roche Diagnostics to develop a sequencing system and assays for clinical diagnostics using its single-molecule real-time sequencing technology in a deal worth up to $75 million.
New England Biolabs has been using Pacific Biosciences’ RS machine to sequence bacterial genomes and study bacterial methylomes.
Researchers at McGill University have developed two different protocols for sequencing bacterial genomes in under 24 hours to monitor outbreaks.
Technology feature describes how recent advances in high-throughput sequencing are accelerating genomics research, but crucial gaps in data remain.
The 100K Genome Project has added 20 newly completed genome sequences of foodborne pathogens to NCBI’s database generated using Pacific Biosciences’ single-molecule sequencing technology.
Nobel Laureate Rich Roberts from New England Biolabs discusses his experience with SMRT Sequencing.
The 100K Genome Project today announced that it has added 20 newly completed genome sequences of foodborne disease-causing microorganisms to its public database at the National Center for Biotechnology Information.
A new technique could soon spur unprecedented insight into the role of bacterial epigenetics in the evolution of pathogen virulence.
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.
Long-read sequencing and Pacific Biosciences are back on the radar after the Advances in Genome Biology & Technology (AGBT) meeting in February in Marco Island, Florida.
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.
Review of several AGBT presentations including, Eric Antoniou and Mike Schatz from Cold Spring Harbor Laboratory, Eric Schadt from Mt. Sinai and PacBio CSO Jonas Korlach.
Scientists from Virginia Bioinformatics Institute and Baylor College of Medicine are using long reads from the PacBio RS to sequence through repeat structures in the human genome
For the first time, researchers sequenced DNA molecules without the need for the standard pre-sequencing workflow known as library preparation.
Long read sequencers combine with short read sequencers for better results in complex genome assembly and finishing.
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