Infographic — Structural variants and disease
Explore the types of human genomic variation and the diseases known to be caused by structural variants.
Explore the types of human genomic variation and the diseases known to be caused by structural variants.
Explore how high-quality genomes contribute to critical scientific endeavors.
Explore how long-read sequencing enables solving of rare and mendelian diseases.
PacBio Systems are powered by Single Molecule, Real-Time (SMRT) Sequencing, a technology proven to produce exceptionally long reads with high accuracy. SMRT Sequencing allows you to accelerate your science with the complete range of PacBio applications to produce data you can trust.
Our understanding of microbiology has evolved enormously over the last 150 years. Few institutions have witnessed our collective progress more closely than the National Collection of Type Cultures (NCTC). In fact, the collection itself is a record of the many milestones microbiologists have crossed, building on the discoveries of those who came before. To date, 60% of NCTC’s historic collection now has a closed, finished reference genome, thanks to PacBio Single Molecule, Real- Time (SMRT) Sequencing. We are excited to be their partner in crossing this latest milestone on their quest to improve human and animal health by understanding the microscopic world.
Explore how highly accurate long-read sequencing enabled sequencing the large and highly complex California redwood genome.
Discover how HiFi reads enable every aspect of viral research, from understanding viral genomes to the host immune response.
If you have a question, need to check the status of an order, or are interested in purchasing an instrument, we're here to help.