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Revio system

Reveal more with accurate long-read sequencing at scale

Most affordable, complete, phased genome

HiFi reads combine long-read length with high accuracy, replacing multiple assays and confidently resolving complex regions beyond the limits of short reads and nanopore methods.

HiFi sequencing at scale, with less DNA input required

Built for population-scale studies and programs that don’t pause. Run up to ~2,500 human whole genomes per year, up to 480 Gb of HiFi reads per day, and up to 4 SMRT Cells simultaneously with configurable run times and flexible scheduling — so sequencing keeps pace with your science.

On-instrument multiomic insight, included

Every standard run delivers on-instrument 5mC and 6mA methylation calling—at no additional cost or bisulfite treatment—giving you access to genomic and epigenetic data from a single sample.

Confidence in every run, without the complexity

HiFi accuracy powered by SPRQ chemistry and Google Health DeepConsensus, paired with an easy, automation-ready workflow supported by compatible partners—so you get reliable results with minimal hands-on time.

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HiFi sequencing at scale

Estonia National Biobank selects PacBio to sequence 10,000 whole genomes

HiFi data generated on the Revio system will support the EU and Estonian government-funded Center for Personalized Medicine to enable discoveries across cardiology, mental and reproductive health, drug response, cancer research and rare diseases.

PacBio and GeneDx Launch Research Collaboration with the University of Washington

This study is first of its kind to compare diagnostic rates across short- and long-read sequencing platforms to understand the potential for increased diagnostic yield in neonatal care.

Ambry Genetics and PacBio Announce Collaboration to Sequence Up to 7,000 Human Genomes

Consortium selects leading genomics companies to support pediatric Mendelian Genomics Research Center Program aimed at providing insights for families battling rare diseases.

Coming soon – SPRQ-Nx Chemistry

Revio system runs on SPRQ chemistry and helps you achieve more with less DNA – empowering you to make more discoveries faster and affordably.

New SPRQ-Nx extends SPRQ chemistry with improved consistency, new 5hmC methylation caller, and multi-use SMRT Cells, enabling a richer and cost-effective HiFi workflow. Built for projects that scale, it maintains the gold-standard HiFi quality you rely on, from population studies to routine panels.

Check SPRQ-Nx availability

SPRQ-NX: BUILT FOR STUDIES THAT KEEP GROWING

Webinar: Scaling HiFi Genomes and Multiomic Discovery with SPRQ-Nx

Get inspired by real-world use of SPRQ-Nx by beta customers.

Watch webinar

SPRQ-Nx public datasets

See for yourself the latest SPRQ-Nx datasets for human, plant + animals.

Read blog

Keep me informed

Be the first to hear SPRQ-Nx updates on performance and release timing.

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Key applications and sample throughput with SPRQ chemistry

The Revio system supports a variety of applications that benefit from accurate long HiFi reads and 500 ng input DNA requirement. Its four independent stages allow different samples and applications to be sequenced in parallel. A subset of key applications is:

Library Application Per Revio SMRT Cell
Per yeara
Expected coverageb
0.5-5 kb Amplicon sequencing > 1,000 > 2.5 million 50X
5-10 kb Microbial genome 384 480,000 30X
5-15 kb PureTarget panels 96 96,000 >100X mean per target
5-10 kb Ampli-Fi human genome 1 1,250 20X
15-20 kb Human genome 2 2,500 20X
15-20 kb Human methylation profiling 8 10,400 5X
15-20 kb Transcriptome with Kinnex full-length RNA kit 6 7,500 10 million reads
  1. Annual throughput is based on 2,500 Revio SMRT Cells for 12 hour runs; 1,250 for 24 hour runs. Adaptive loading – which increases the consistency of yield per SMRT Cell – adds about 4 hours to run time, affecting the maximum number of SMRT Cells per year. 
  2. Expected coverages are estimates. 

See what you can get from 1 SMRT Cell   Access data sets

“HiFi long read sequencing can now produce the most comprehensive variant dataset obtainable by a single technology in a single laboratory, allowing accurate calling of substitutions, indels, STRs and SVs.”

– Kucuk et al., Genome Med, 2023

HIFI LEVEL ACCURACY AND DATA QUALITY

The Revio system with SPRQ chemistry produces exceptional read length, quality, and variant calling performance that have made HiFi sequencing so celebrated.

Reveal a more complete genome

The complete, gapless human genome marks a new era of genomics where no region of the genome is beyond your reach. In 2021, PacBio HiFi technology was used by the Telomere-to- Telomere (T2T) Consortium to fill in those gaps.

Read length

HiFi reads are tens of kilobases long, providing the ability to resolve large variants and map to difficult regions of the genome.

Read and base quality

The Revio system provides reliable answers through exceptional accuracy, with 90% of bases Q30+ and median read accuracy ≥Q30.

Variant calling

HiFi sequencing with SPRQ chemistry on the Revio system delivers high accuracy variant detection, resulting in fewer sequencing errors relative to other technologies at lower coverage1.

How Revio long-read sequencing compares

PacBio Revio with SPRQ SBS sequencing Nanopore sequencing
Read length

15-20 kb5

2x150 bp 10–100 kb
Read accuracy

99.95% (Q33)1

99.92% (Q31)3

98.90% (Q19)4

Run time

24 hours2

44 hours 72 hours
Yield

120 - 480 Gb2

2,400–3,000 Gb 50–110 Gb
Coverage Unbiased Reduced at low and high (GC) Reduced in low-complexity runs

Genome completeness6

X

Variant calling – SNVs, Indels, SVs5

X
X
Areas of high homology
X
X
Phasing
X
Methylation Every run Via library prep Every run

1. Read accuracy PacBio HiFi: precisionFDA Truth Challenge V2
2. HiFi yield specification based on HG002/GM24385 human DNA extracted with Nanobind CBB kit and prepared with SMRTbell prep kit 3.0. Run time specification is for the sequencing reaction. HiFi yield is dependent on library fragment size. Yield is typically lower for shorter libraries.

3. Illumina: HG002 2×150 bp NovaSeq library, precisionFDA Truth Challenge V2
4. ONT: Q20+ chemistry (R10.4, Kit 12), Oct 2021 GM24385 Q20+ Simplex dataset release
5. Shafin Nat Methods 2021 (https://doi.org/10.1038/s41592-021-01299-w)
6. Cheng 2021 Nat Methods (https://doi.org/10.1038/s41592-020-01056-5) and Shafin 2020 Nat Biotech (https://doi.org/10.1038/s41587-020-0503-6)

 

Workflow

Extraction

Nanobind DNA kits enable extraction of HMW gDNA from a variety of samples: saliva, cultured cells, bacteria, whole blood, tissue, plant nuclei, and insect.

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Library prep

SMRTbell prep kit 3.0, HiFi prep kits, and application kits (Kinnex, PureTarget) support manual and automated library prep for effortless SMRTbell library creation.

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Sequencing

Built for scale and flexibility, Revio lets you run 4 SMRT Cells at once, and scheduling that fits your lab.

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Data analysis

Advanced algorithms from Google Health and cutting-edge NVIDIA GPUs allow for on-board processing of sequencing data, all with reduced output file sizes.

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Simplified Consumables

The Revio system simplifies the HiFi sequencing experience with fewer consumables optimized for easy tracking and minimal waste. With workflow improvements, loading consumables takes under a minute at the instrument.

Revio SMRT Cell tray

One tray contains 4 high-density SMRT Cells.

Revio SPRQ sequencing plate

The sequencing plate provides reagents for sequencing up to 4 Revio SMRT Cells.

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A WORKFLOW BUILT FOR YOUR SCHEDULE

The Revio system gives you a vastly simplified experience with consumables and software designed for flexibility and convenience. Whether you’re a genome center or a small lab, you can enjoy:

Fast, reliable library preparation

Library prep for the Revio system supports manual and automated prep. Learn more

Rapid run setup

Sequencing plates are linked automatically to run designs through an NFC tag, enabling runs to be set up in less than one minute on instrument.

Flexibility to fit your schedule

The Revio work deck is isolated from the four sequencing stages, leaving the system available up to 20 hours per day for loading consumables for subsequent runs.

MASSIVE COMPUTE POWER

The Revio system includes powerful NVIDIA GPUs, which provide more than 20× the compute power of the Sequel IIe system, to deliver accurate, ready-to-use data directly from the instrument.

HiFi read generation

The GPUs provide rapid turnaround time for basecalling and HiFi read generation, directly outputting HiFi reads in BAM format.

Google Health DeepConsensus

DeepConsensus uses advanced deep learning techniques to further extend the accuracy and yield of HiFi sequencing.

Methylation calling (5mC and 6mA)

Standard runs include DNA methylation status, calculated with a deep learning algorithm that processes polymerase kinetics.

Demultiplexing

All fundamental processing steps are performed on instrument, including barcode demultiplexing.

 

Image of Revio system with Google Health logo in front

More HiFi reads, more samples, more discovery

System specifications with SPRQ chemistry

The Revio system utilizes nanofabricated Revio SMRT Cells and has four independent stages, allowing sequencing of multiple SMRT Cells in parallel. The onboard compute provides accurate basecalling with Google DeepConsensus, plus methylation calling in every run.

Library
Run timea
Q30+ bases

HiFi yield per SMRT Cellb

Methylation
0.5-5 kb 12 hours 95% 6-8 million reads 5mC at CpG sites and 6mA for native DNAc
5-10 kb 24 hours 90% 35-70 Gb
10-15 kb 70-100 Gb
15-20 kb 100-120 Gb
20-25 kb 30 hours 85% 100-120 Gb
  1. Run time refers to the data collection step, which determines the time between processing SMRT Cells.
  2. HiFi yield is dependent on library quality and sequencing preparation procedures.  Specified yield is based on high-quality samples prepared following best practices. 
  3. The Revio 6mA caller is designed to detect methylation in the context of the Fiber-seq chromatin assay.

Download spec sheet

 

Instrument specifications

Operating environment
Temperature 19–25°C (66–77°F)
Humidity 20–80% relative humidity, non-condensing
Ventilation 13,000 BTU/hr (3,800 W)
Dimensions
W × D × H 92.7 cm (36.5 in) × 91.4 cm (36.0 in) × 174.5 cm (68.7 in)
Weight 465 kg (1,025 lb)
Floor space 243.8 cm (96.0 in) × 138.5 cm (54.5 in)
Electrical power
Power requirements 200–240 VAC at 50-60 Hz, max 5 kVA/4.8 kW/24A
Compute
Network connection 1 GbE or 10 GbE, copper
Output file format hifi_reads.bam, ~60 GB each, up to 78 TB per year

Frequently asked questions

SPRQ (pronounced “spark”) is PacBio’s newest HiFi chemistry, designed to make sequencing more efficient and expand HiFi sequencing to more sample types and applications. It requires only 500 ng of native DNA, opening up new possibilities for challenging or precious samples. SPRQ also helps reduce genome costs by increasing HiFi yields per SMRT Cell by 33%, enabling sequencing of two human genomes at 20X coverage per SMRT Cell. In addition, SPRQ supports deeper multiomic insights into chromatin architecture with Fiber-seq, featuring on-instrument 5mC and 6mA calling for greater precision in methylation detection.

SPRQ-Nx (pronounced “next”) is an update to SPRQ chemistry that increases data consistency, new 5hmC methylation caller, and introduces a new multi-use SMRT Cell that can be used for multiple acquisitions on the Revio system. “Nx” represents that a SMRT Cell can be used “N” times and is the next evolution in HiFi sequencing.

SPRQ-Nx is currently in beta testing and will be available in Q2-2026. Want to be among the first to hear the latest news about SPRQ-Nx?

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The Revio system with SPRQ chemistry sequences two human genomes at 20x coverage for just $5006. Your local sales representative can provide detailed pricing in your currency.

6$500 per human HiFi genome assumes US list price of $995 for sequencing reagents for one Revio SPRQ SMRT Cell, which has an expected yield of 120 Gb, equivalent to two 20× human genomes.

The capabilities† of just one Revio SMRT Cell include:

  • Up to 120 Gb of total HiFi long-read sequencing data in 24 hours.
  • Two phased 20x human whole genome.
  • One sample with ~80 million full-length RNA isoforms using the Kinnex single-cell RNA kit.
  • 16 samples using large, targeted gene panels such as the Dark Gene.
  • 96 samples using small, targeted gene panels similar to the Long-read PGx.
  • 16 communities of metagenome assembled genomes.

† Expected coverage and throughput are estimates. Coverage and total reads/data may vary based on library quality and fragment lengths.

The Revio system outputs ready-to-use HiFi reads in BAM format. All fundamental processing steps are performed on instrument, including barcode demultiplexing.

  1. Data shown is for a single Revio SMRT Cell for HG002/GM24385.
  2. HiFi yield specification based on HG002/GM24385 human DNA extracted with Nanobind CBB kit and prepared with SMRTbell prep kit 3.0.
  3. Run time specification is for the sequencing reaction.
  4. Expected coverages and throughputs are estimates. Coverage may vary based on library quality and fragment lengths.
  5. HiFi yield is dependent on library fragment size. Yield is typically lower for shorter libraries.
  6. Currency is calculated based on reagent list pricing in USD.

See system specification sheet for more details.

EXPLORE THE REVIO SYSTEM

Take a 3D tour of the Revio system to see key features, setup, workflows or request a quote.

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