Out with the old, in with Onso. Now $99k with the trade-in of any non-PacBio NGS system.
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Detecting cancer fusion transcripts in long-read RNA-Seq data with CTAT-LR-fusion
In this webinar, you will learn about CTAT-LR-fusion, a new bioinformatics tool for detecting known and novel fusion transcripts from PacBio long-read isoform sequencing data, with applications to bulk and single-cell tumor transcriptomes.
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.
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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.
![Image of a flowcell](https://www.pacb.com/wp-content/uploads/img_masonry_flowcell.png)
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.
![Image of a PacBio SMRT Cell over a blue background](https://www.pacb.com/wp-content/uploads/img_masonry_smrt_cell.png)
What can you do with a Revio system?
Access more information at reduced cost and higher throughput with Revio long-read sequencing.