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    • Cleavage Under Targets & Tagmentation (CUT&Tag) New!
    • Assay for Transposase-Accessible Chromatin with Sequencing (ATAC-seq)
    • Reduced Representation Bisulfite Sequencing (RRBS)

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    • Quantitative Proteomics New!
    • PTM Proteomics New!
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    • mRNA Sequencing
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  4. Novogene's Revio Data: Achieving Maximum 110Gb HiFi Reads per SMRT Cell!

Novogene's Revio Data: Achieving Maximum 110Gb HiFi Reads per SMRT Cell!

Novogene has recently installed PacBio’s latest high-throughput sequencing system—Revio. Revio delivers exceptional performance in terms of throughput with excellent base quality. This cutting-edge technology promises a historically high throughput of 360 Gb of HiFi reads per day, making a significant 15× increase compared to the previous Sequel II system. Novogene has validated runs with DNA HiFi libraries of plants, animals and human. The results show that the system may produce a maximum output of up to 110.5 Gb per SMRT cell, which surpass the standard data output of 90Gb per SMRT cell published by PacBio. The enhanced capabilities of Revio system will allow Novogene to add high throughput to HiFi long reads sequencing and direct methylation detection for a wide array of applications.

1.HiFi yield per SMRT cell of Revio system

The average data output per SMRT cell is 98.4Gb, with a quality value of 31.2. Additionally, the platform demonstrates a maximum data output of 110.5 Gb per SMRT cell.

Table 1 Quality control result of Revio sequencing data

SampleHiFi Yield (Gb)Read Length(mean) (bp)Read Length(N50) (bp)Mean Quality Value
Human Sample 1110.521,31321,96731.3
Animal Sample 198.316,30516,48631.1
Plant Sample 186.419,65919,95331.1
2.Testing results of multiplexed libraries

DNA multiplexed libraries, consisting of three animal samples and three plant samples are sequenced on Revio system respectively. The results show that each animal sample yields more than 30Gb HiFi reads, and the data demultiplexing rate reaches a level of more than 99%.

Table 2 Quality control result of multiplexed SMRT cell libraries

SampleTotal HiFi Yield (Gb)Data Demultiplexing Rate (%)Single-sample HiFi Yield (Gb)Read Length(mean) (bp)Read Length(N50) (bp)
Animal 1102.399.5632.020,63420,558
Animal 234.219,52319,464
Animal 335.719,07418,988
Plant 184.699.7630.017,15717,002
Plant 223.116,63416,614
Plant 331.216,51316,320
3.Comparison of sequencing data achieved on Sequel II system and Revio

Human and plant gDNA samples are used for HiFi library preparation and sequenced on PacBio’s Sequel II system and Revio system respectively to evaluate the performance differences. The results indicate that the Revio system is able to yield 2-3 times more HiFi data per SMRT cell compared to Sequel II. Furthermore, Revio completes the sequencing in a shorter run time, while maintaining a mean data quality > Q30.

Table 3 Sequel II system vs Revio system sequencing data

Sample SystemHiFi Yield (Gb)Read length(mean) (bp)Read length(N50) (bp)Run times (h)Mean quality value
Human Sample 1Sequel II38.420,42020,3453031.0
Human Sample 1Revio110.521,31321,9672431.3
Plant Sample 1Sequel II31.815,46215,5553031.1
Plant Sample 1Revio84.618,79919,3382431.1
4.Data analysis of human whole genome sequencing on Revio system

The achieved mapping rate of human whole genome is 99.91%, with coverage across the entire genome of 99.64% and an average sequencing depth of 38X.

Table 4 Mapping statistics of human samples sequenced on the Revio system.

SpeciesHiFi Yield (Gb)Clean ReadsMapped ReadsMapping Rate (%)1X Coverage Rate (%)4X Coverage Rate (%)10X Coverage Rate (%)20X Coverage Rate (%)Mean Depth
Human Sample110.5G5,555,6915,550,504.0099.9199.6499.2698.6794.3738
a
b

Figure 1 Analysis results of human whole genome resequencing (WGS) data

Figure 1. (a): Statistics of structural variation length. (b): The circos figure shows the density of variant chromosome distribution, including translocation, insertion, deletion, inversion, copy number variation, short tandem repeat, gene, chromosome.

About Novogene
Novogene is a pioneer in applying cutting-edge molecular biology technology and high-performance computing to research in the fields of life science and human health. Our vision is to be the leader in providing genomic services and solutions.

Novogene has extensive coverage in genome projects and has accumulated vast experiences in third-generation library preparation, sequencing, and bioinformatics analysis for numerous species. Novogene has technical advantages in de novo sequencing technology and applications, holding 18 patent licenses and over 40 software copyrights. Our vision is to be the leader in providing genomic services and solutions.

With one of the largest sequencing capacities in the world, we utilize our deep scientific knowledge, first-class customer service, and unsurpassed data quality to help clients realize their research goals in the rapidly evolving world of genomics. Novogene is committed to becoming your trusted genomics partner.

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mRNA SequencingSwift & Express mRNA SequencingTotal RNA SequencingHuman Whole Genome SequencingWhole Exome Sequencing10x Single Cell Gene ExpressionIllumina PIP-seq Single Cell 3’ RNA SequencingSpatial Transcriptomics SequencingWhole Genome Bisulfite Sequencing (WGBS)Quantitative ProteomicsUntargeted MetabolomicsShotgun Metagenomics SequencingMetatranscriptome SequencingSequencing Only on Illumina SequencerSequencing Only on Ultima SequencerFull-Length Transcriptome SequencingChromatin Immunoprecipitation Sequencing (ChIP-seq)
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Copyright © 2026 Novogene Corporation Inc. All rights reserved. For Research Use Only.
    • Cart
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Novogene
  • Novogene
  • Genomics
    • Human Whole Genome Sequencing
    • Whole Exome Sequencing
    • Plant and Animal Whole Genome Sequencing
    • Plant and Animal De Novo Sequencing
    • Microbial Whole Genome Sequencing
    • Microbial De Novo Sequencing

    Metagenomics

    • Shotgun Metagenomics Sequencing
    • Amplicon Sequencing

    Transcriptomics

    • mRNA Sequencing
    • Swift & Express mRNA Sequencing New!
    • Full-Length Transcriptome Sequencing
    • Prokaryotic RNA Sequencing
    • Metatranscriptome Sequencing
    • Total RNA Sequencing
    • Small RNA Sequencing (sRNA‑seq)
    • Whole Transcriptome Sequencing

    Single Cell & Spatial Omics

    • 10x Single Cell Gene Expression
    • Illumina PIP-seq Single Cell 3’ RNA Sequencing New!
    • Spatial Transcriptomics Sequencing New!

    Epigenomics

    • Whole Genome Bisulfite Sequencing (WGBS)
    • Enzymatic Methylation Sequencing
    • Directed Methylation Sequencing (DM-Seq) New!
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • Cleavage Under Targets & Tagmentation (CUT&Tag) New!
    • Assay for Transposase-Accessible Chromatin with Sequencing (ATAC-seq)
    • Reduced Representation Bisulfite Sequencing (RRBS)

    Proteomics

    • Quantitative Proteomics New!
    • PTM Proteomics New!
    • Olink Proteomics New!

    Metabolomics

    • Untargeted Metabolomics

    Premade Library

    • Sequencing Only on Illumina Sequencer
    • Sequencing Only on Ultima Sequencer
  • PromotionsPromotions
    • Platforms
    • Service & Support
    • Automated Delivery Platform (Falcon)
    • Bioinformatics Analysis Tool (NovoMagic)
    • Customer Service System (CSS)
    • Case Study
    • Blog
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    • Brochure
    • Cancer Research
    • Immuno-oncology
    • Agrigenomics
    • Environment
    • Food Science
    • Human Microbiome
    • Plant and Animal Microbiome
    • Drug Discovery and Development
    • Rare and Complex Diseases
    • About Us
    • Our Locations
    • News & Events
    • Careers
  • Contact UsContact Us
    • mRNA Sequencing
    • Illumina Lane Sequencing
  1. Home
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  4. Novogene's Revio Data: Achieving Maximum 110Gb HiFi Reads per SMRT Cell!

Novogene's Revio Data: Achieving Maximum 110Gb HiFi Reads per SMRT Cell!

Novogene has recently installed PacBio’s latest high-throughput sequencing system—Revio. Revio delivers exceptional performance in terms of throughput with excellent base quality. This cutting-edge technology promises a historically high throughput of 360 Gb of HiFi reads per day, making a significant 15× increase compared to the previous Sequel II system. Novogene has validated runs with DNA HiFi libraries of plants, animals and human. The results show that the system may produce a maximum output of up to 110.5 Gb per SMRT cell, which surpass the standard data output of 90Gb per SMRT cell published by PacBio. The enhanced capabilities of Revio system will allow Novogene to add high throughput to HiFi long reads sequencing and direct methylation detection for a wide array of applications.

1.HiFi yield per SMRT cell of Revio system

The average data output per SMRT cell is 98.4Gb, with a quality value of 31.2. Additionally, the platform demonstrates a maximum data output of 110.5 Gb per SMRT cell.

Table 1 Quality control result of Revio sequencing data

SampleHiFi Yield (Gb)Read Length(mean) (bp)Read Length(N50) (bp)Mean Quality Value
Human Sample 1110.521,31321,96731.3
Animal Sample 198.316,30516,48631.1
Plant Sample 186.419,65919,95331.1
2.Testing results of multiplexed libraries

DNA multiplexed libraries, consisting of three animal samples and three plant samples are sequenced on Revio system respectively. The results show that each animal sample yields more than 30Gb HiFi reads, and the data demultiplexing rate reaches a level of more than 99%.

Table 2 Quality control result of multiplexed SMRT cell libraries

SampleTotal HiFi Yield (Gb)Data Demultiplexing Rate (%)Single-sample HiFi Yield (Gb)Read Length(mean) (bp)Read Length(N50) (bp)
Animal 1102.399.5632.020,63420,558
Animal 234.219,52319,464
Animal 335.719,07418,988
Plant 184.699.7630.017,15717,002
Plant 223.116,63416,614
Plant 331.216,51316,320
3.Comparison of sequencing data achieved on Sequel II system and Revio

Human and plant gDNA samples are used for HiFi library preparation and sequenced on PacBio’s Sequel II system and Revio system respectively to evaluate the performance differences. The results indicate that the Revio system is able to yield 2-3 times more HiFi data per SMRT cell compared to Sequel II. Furthermore, Revio completes the sequencing in a shorter run time, while maintaining a mean data quality > Q30.

Table 3 Sequel II system vs Revio system sequencing data

Sample SystemHiFi Yield (Gb)Read length(mean) (bp)Read length(N50) (bp)Run times (h)Mean quality value
Human Sample 1Sequel II38.420,42020,3453031.0
Human Sample 1Revio110.521,31321,9672431.3
Plant Sample 1Sequel II31.815,46215,5553031.1
Plant Sample 1Revio84.618,79919,3382431.1
4.Data analysis of human whole genome sequencing on Revio system

The achieved mapping rate of human whole genome is 99.91%, with coverage across the entire genome of 99.64% and an average sequencing depth of 38X.

Table 4 Mapping statistics of human samples sequenced on the Revio system.

SpeciesHiFi Yield (Gb)Clean ReadsMapped ReadsMapping Rate (%)1X Coverage Rate (%)4X Coverage Rate (%)10X Coverage Rate (%)20X Coverage Rate (%)Mean Depth
Human Sample110.5G5,555,6915,550,504.0099.9199.6499.2698.6794.3738
a
b

Figure 1 Analysis results of human whole genome resequencing (WGS) data

Figure 1. (a): Statistics of structural variation length. (b): The circos figure shows the density of variant chromosome distribution, including translocation, insertion, deletion, inversion, copy number variation, short tandem repeat, gene, chromosome.

About Novogene
Novogene is a pioneer in applying cutting-edge molecular biology technology and high-performance computing to research in the fields of life science and human health. Our vision is to be the leader in providing genomic services and solutions.

Novogene has extensive coverage in genome projects and has accumulated vast experiences in third-generation library preparation, sequencing, and bioinformatics analysis for numerous species. Novogene has technical advantages in de novo sequencing technology and applications, holding 18 patent licenses and over 40 software copyrights. Our vision is to be the leader in providing genomic services and solutions.

With one of the largest sequencing capacities in the world, we utilize our deep scientific knowledge, first-class customer service, and unsurpassed data quality to help clients realize their research goals in the rapidly evolving world of genomics. Novogene is committed to becoming your trusted genomics partner.

ServicesServices menu

CompanyCompany menu

Contact UsContact Us menu

Service SupportService Support menu

Services
mRNA SequencingSwift & Express mRNA SequencingTotal RNA SequencingHuman Whole Genome SequencingWhole Exome Sequencing10x Single Cell Gene ExpressionIllumina PIP-seq Single Cell 3’ RNA SequencingSpatial Transcriptomics SequencingWhole Genome Bisulfite Sequencing (WGBS)Quantitative ProteomicsUntargeted MetabolomicsShotgun Metagenomics SequencingMetatranscriptome SequencingSequencing Only on Illumina SequencerSequencing Only on Ultima SequencerFull-Length Transcriptome SequencingChromatin Immunoprecipitation Sequencing (ChIP-seq)
Company
About UsOur LocationsNews & EventsCareers
Contact Us
Contact Us
Service Support
Automated Delivery Platform (Falcon)Bioinformatics Analysis Tool (NovoMagic)Customer Service System (CSS)
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Copyright © 2026 Novogene Corporation Inc. All rights reserved. For Research Use Only.
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