SPRING PROMOS, STILL BLOOMING
Revio systems, now available at nearly 50% off up front with reagent bundles
APPLY NOW TO THE AAV Star GRANT
Apply to win free sequencing plus a travel stipend to enhance and promote your gene and cell therapy research.
Upcoming webinar
Webinar: May 8-9, 2024 — COMPREHENSIVE VARIANT DETECTION IN PEDIATRIC LEUKEMIA RESEARCH WITH ACCURATE LONG-READ WHOLE GENOME SEQUENCING
Coming to a city near you
Introducing PacBio PRISM 2024, designed to cast a full spectrum of light on the boundless possibilities in genomics.
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.
