Ignite your research with the new SPRQ chemistry on Revio
Experience HiFi sequencing at scale with the new SPRQ chemistry on Revio – a powerful upgrade that delivers up to 480 Gb of HiFi reads per day and enabling the sequencing of 2,500 human genomes per year. With just 500 ng of DNA, you can now generate phased genomes, detect variants, full-length transcripts, methylation (5mC and 6mA), and repeat expansions, all from a single library and run.
Register now for PAG 2025
Book time with our experts on-site, preview our workshop, or receive videos and other content we present at PAG 2025. Stop by our booth #219 to chat with PacBio staff and get a hands-on demonstration of our new Vega benchtop sequencer.
Bringing HiFi to the benchtop
The Vega system delivers 60 Gb of the most accurate long reads per run. Get complete genomic, transcriptomic, and epigenetic data – tailored for individual labs. With Vega, you take full control, streamlining your projects and saving time by sequencing in-house. Your lab, your discoveries – faster than ever!
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.
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.
Accelerate your research
Application note
Kinnex full-length RNA Kit for isoform sequencing
The Kinnex full-length RNA kit for bulk RNA sequencing produces 15 million reads and 40 million reads per SMRT Cell on Sequel II and Revio systems. This represents a 15-fold throughput increase on Revio with Kinnex.
The value of Q40+ sequencing for liquid biopsy
Onso short-read sequencing can reduce false positives and improve sensitivity for detecting rare variants in ctDNA.
Sequencing 101: SBB sequencing
Sequencing by binding (SBB) technology allows you to generate extraordinarily accurate reads with an error rate of only 1 in 10,000 bases or less.
What can you do with a Revio system?
Access more information at reduced cost and higher throughput with Revio long-read sequencing.
