June 20 and June 22
Shining a light on dark genes in population sequencing: Hear how HiFi long-read sequencing is energizing the potential of population genomics
DNA extraction
New Nanobind® high-throughput (HT) kits enable automation of DNA extraction on four robotic platforms
Learn moreSequencing methods for solutions that matter
Our technology provides the most comprehensive view of genomes, transcriptomes, and epigenomes.
Whole genome sequencing
Achieve the highest consensus accuracy and uniform coverage for reference quality genomes in humans, plants, animals, and microbes.
Targeted sequencing
Accurately detect and uncover all variant types even in hard-to-reach regions of the genome.
Epigenetics
Explore how epigenetic changes affect gene expression, host-pathogen interactions, environmental response, and more.
RNA sequencing
Discover new genes, transcripts, and alternative splicing events with a complete view of transcript isoform diversity.
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The HiFi difference – large-scale, high-quality data for all of us
As the main finding, the authors in a new preprint entitled Utility of long-read sequencing for All of Us state that “HiFi reads produced the most accurate results for both small and large variants” and conclude that “long reads have widespread value for establishing the most complete and accurate variant calls for All of Us and potentially for many other projects.”
THWART FOOD-BORNE CONTAMINANTS WITH HIGHLY ACCURATE HIFI SEQUENCING
HiFi sequencing delivers highly accurate and comprehensive microbial sequence data possible to give food safety and public health professionals the clarity they need to better understand contaminants and make informed and timely decisions.
PIECING TOGETHER THE PUZZLE OF GENETIC DISEASE
Watch how scientists use whole genome sequencing and single-cell RNA sequencing to shed light on unresolved neurological medical mysteries.
Sequence with confidence using PacBio sequencing systems
Explore the advantages of PacBio highly accurate short-read and long-read sequencing technologies.
OUR PURPOSE
IS YOUR PURSUIT
We deliver sequencing technologies with exceptionally accurate and comprehensive genomics data so that you can find answers where others have only found questions.
We strive to miss nothing, so you can do anything.