The 2022 Plant + Animal Sciences SMRT Grant is open
Could your Plant + Animal research benefit from highly accurate long-read sequencing? Apply to win free sequencing. Application submission deadline: October 7, 2022 at 5 PM PDT.Apply now
The HiFi Difference
A single solution, set apart from other technologies. From the largest organisms to the smallest microbes, HiFi sequencing empowers answers to biology’s toughest questions.Explore the difference
What would you do with 5-base sequencing?
Our latest system release introduces 5-base HiFi sequencing to detect 5mC methylation in CpG motifs in standard sequencing runs. No changes are required to library prep or sequencing workflows.See what's new
Sequencing methods for solutions that matter
Whole genome sequencing
Achieve the highest consensus accuracy and uniform coverage for reference quality genomes in humans, plants, animals, and microbes.
Accurately detect and uncover all variant types even in hard-to-reach regions of the genome.
Accelerate your research
CUSTOMER SUCCESS STORY
EXPERTS AT CHILDREN’S MERCY KANSAS CITY USE LONG-READ SEQUENCING TO SHED LIGHT ON RARE DISEASE
Scientists at the Children’s Mercy Research Institute use PacBio technology to shed light on rare diseases that conventional sequencing approaches could not find.
THWART FOOD-BORNE CONTAMINANTS WITH THE UNMATCHED ACCURACY OF HIFI SEQUENCING
HiFi sequencing delivers the most 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
NOW ON DEMAND: Watch how two scientists use whole genome sequencing and single-cell RNA sequencing to shed light on unresolved neurological medical mysteries.
Sequence with confidence using PacBio highly accurate long reads
Explore the advantages of the Sequel II and IIe systems with HiFi sequencing technology.
IS YOUR PURSUIT
We deliver sequencing technologies with the most 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.