Streamline HiFi sequencing: introducing SMRT Link Cloud
Whether you’re just getting started or looking to transition over to a cloud-first solution, this webinar will cover all you need to know, including the different versions of SMRT Link, technical details of SMRT Link Cloud, and how to get started. This webinar will be of interest to researchers, lab managers, and IT professionals using or considering the PacBio Revio or Vega systems.
Episode 3: Half way there, but it’s just getting started
Shana McDevitt. She’s seen it all, but this is the one thing that stopped her cold…
Sign up now to see how smart planning helps labs keep their timelines (and sanity) intact—even when sample quality is tricky and unlock all four episodes before they’re gone.
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.
