Ampli-Fi: unlocking HiFi sequencing for low-input and challenging samples
In this webinar, learn how Ampli-Fi opens new possibilities for challenging or previously inaccessible sample types such as insects, metagenomic samples, low-volume biopsies, FFPE tissues, ethanol-preserved specimens, and marine invertebrates. Explore capabilities such as its integration with CiFi (HiFi-compatible 3C), and discover how researchers are using it to generate reference-quality genome assemblies from limited or degraded DNA.
Powering the Future of ALS Research with Long-Read Sequencing
In this webinar, Target ALS will share why they chose PacBio HiFi sequencing for sequencing up to 6,000 genomes in the largest ALS genomics study to date. Learn how HiFi long-read data is revealing hidden variants missed by short reads—and how open access to this data is accelerating global ALS research.
Apply now for the 2025 Microbiome SMRT Grant program
Discover enhanced resolution of metagenomics and microbiomes by applying to win free sequencing through the Microbiome SMRT Grant program. If chosen to win, you will receive free HiFi sequencing for your research that furthers global health.
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.
