Novogene AMEA
  • Novogene AMEA
  • Genomics
    • Human Whole Genome Sequencing
    • Plant and Animal Whole Genome Sequencing
    • Microbial Whole Genome Sequencing
    • Plant and Animal De novo Sequencing
    • Microbial De novo Sequencing
    • Shotgun Metagenomics Sequencing
    • Amplicon Sequencing
    • Whole Exome Sequencing
    Transcriptomics
    • mRNA Sequencing
    • Total RNA Sequencing
    • Full-Length Transcriptome Sequencing
    • Whole Transcriptome Sequencing
    • Small RNA Sequencing
    • Circular RNA Sequencing
    • Metatranscriptome Sequencing
    • Prokaryotic RNA Sequencing
    Single Cell & Spatial Omics
    • Single Cell Gene Expression
    • Single Cell Immune Profiling Sequencing
    • Single Cell Long Read Transcriptome
    • Visium HD Spatial Gene Expression
    • Stereo-Seq Spatial Gene Expression
    • Xenium In Situ Spatial Transcriptome
    Epigenomics
    • Whole Genome Bisulfite Sequencing (WGBS)
    • Directed DNA Methylation Sequencing (DM-Seq) NEW
    • Reduced Representation Bisulfite Sequencing (RRBS)
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    • Assay for Transposase-Accessible Chromatin with Sequencing (ATAC-seq)

    Premade Library

    • Sequencing Only on Illumina Sequencer
    • Sequencing Only on PacBio Sequencer
    Proteomics and Metabolomics
    • Olink Proteomics
    • Quantitative Proteomics
    • Untargeted Metabolomics
  • PromotionsPromotions
    • Platforms
    • Automated Delivery Platform (Falcon)
    • Bioinformatics Analysis Tool (NovoMagic)
    • Customer Service System (CSS)
    • Brochures
    • Case Studies
    • Webinar
    • Blog
    • Sample Guidelines
    • 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
    • Careers
  • Contact UsContact Us

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Services
Whole Genome SequencingDe novo SequencingAmplicon SequencingShotgun Metagenomic SequencingDirected DNA Methylation Sequencing (DM-Seq)mRNA SequencingSingle Cell Gene ExpressionVisium HD Spatial Gene ExpressionXenium In Situ Spatial TranscriptomeOlink ProteomicsUntargeted Metabolomics
Support
NovoMagic Bioinformatics Analysis ToolCustomer Service SystemFalcon Intelligent Delivery Platform
Company
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Copyright © 2026 Novogene Inc. All rights reserved.For Research Use Only. Not for Clinical Diagnostic Use.
Novogene AMEA
  • Novogene AMEA
  • Genomics
    • Human Whole Genome Sequencing
    • Plant and Animal Whole Genome Sequencing
    • Microbial Whole Genome Sequencing
    • Plant and Animal De novo Sequencing
    • Microbial De novo Sequencing
    • Shotgun Metagenomics Sequencing
    • Amplicon Sequencing
    • Whole Exome Sequencing
    Transcriptomics
    • mRNA Sequencing
    • Total RNA Sequencing
    • Full-Length Transcriptome Sequencing
    • Whole Transcriptome Sequencing
    • Small RNA Sequencing
    • Circular RNA Sequencing
    • Metatranscriptome Sequencing
    • Prokaryotic RNA Sequencing
    Single Cell & Spatial Omics
    • Single Cell Gene Expression
    • Single Cell Immune Profiling Sequencing
    • Single Cell Long Read Transcriptome
    • Visium HD Spatial Gene Expression
    • Stereo-Seq Spatial Gene Expression
    • Xenium In Situ Spatial Transcriptome
    Epigenomics
    • Whole Genome Bisulfite Sequencing (WGBS)
    • Directed DNA Methylation Sequencing (DM-Seq) NEW
    • Reduced Representation Bisulfite Sequencing (RRBS)
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    • Assay for Transposase-Accessible Chromatin with Sequencing (ATAC-seq)

    Premade Library

    • Sequencing Only on Illumina Sequencer
    • Sequencing Only on PacBio Sequencer
    Proteomics and Metabolomics
    • Olink Proteomics
    • Quantitative Proteomics
    • Untargeted Metabolomics
  • PromotionsPromotions
    • Platforms
    • Automated Delivery Platform (Falcon)
    • Bioinformatics Analysis Tool (NovoMagic)
    • Customer Service System (CSS)
    • Brochures
    • Case Studies
    • Webinar
    • Blog
    • Sample Guidelines
    • 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
    • Careers
  • Contact UsContact Us

ServicesServices menu

SupportSupport menu

CompanyCompany menu

Services
Whole Genome SequencingDe novo SequencingAmplicon SequencingShotgun Metagenomic SequencingDirected DNA Methylation Sequencing (DM-Seq)mRNA SequencingSingle Cell Gene ExpressionVisium HD Spatial Gene ExpressionXenium In Situ Spatial TranscriptomeOlink ProteomicsUntargeted Metabolomics
Support
NovoMagic Bioinformatics Analysis ToolCustomer Service SystemFalcon Intelligent Delivery Platform
Company
About UsOur LocationsOur PlatformsNewsCareersContact Us
LinkedInLinkedIn hoverYouTubeYouTube hoverXX hover
Copyright © 2026 Novogene Inc. All rights reserved.For Research Use Only. Not for Clinical Diagnostic Use.
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Sequencing Only on Illumina Sequencer

High-quality short-read sequencing of customer-prepared libraries on the Illumina platform to support diverse genomic and transcriptomic applications.
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(Sequencing Only on Illumina Sequencer)
Request a Quote
(Sequencing Only on Illumina Sequencer)
OverviewOverview
BenefitsBenefits
ApplicationsApplications
SpecificationsSpecifications
ResourcesResources

Novogene provides cost-effective sequencing-only services for customer-prepared, ready-to-sequence libraries on the NovaSeq platform series, including NovaSeq X Plus and NovaSeq 6000.


With a flexible range of sequencing solutions, we offer multiple read length options, scalable throughput configurations, and efficient turnaround times to support the diverse needs of research projects.


Supported by an experienced technical and operations team, Novogene combines solid scientific expertise, strict quality control standards, extensive project experience, and streamlined workflows to deliver reliable, efficient sequencing services - providing consistent data quality and dependable support throughout the entire project lifecycle.

Why Choose Illumina Seq-Only Services with Novogene?

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Why Choose Illumina Seq-Only Services with Novogene?

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Applications of Pre-made Library Sequencing

Novogene’s pre-made library sequencing services offer a flexible and cost-effective solution for research teams with established library preparation workflows.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Applications of Pre-made Library Sequencing

Novogene’s pre-made library sequencing services offer a flexible and cost-effective solution for research teams with established library preparation workflows.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Specifications

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Specifications

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Project Deliverables

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High-Quality Raw Sequencing Data

Receive high-quality raw sequencing data in FASTQ format. For lane sequencing or flowcell sequencing orders, BCL-format data are also available. All deliverables include a comprehensive quality control (QC) report to ensure data reliability.

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Flexible Bioinformatics Solutions

Optional bioinformatics analysis services are available upon request to support downstream interpretation and discovery, tailored to your research needs.

Project Deliverables

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High-Quality Raw Sequencing Data

Receive high-quality raw sequencing data in FASTQ format. For lane sequencing or flowcell sequencing orders, BCL-format data are also available. All deliverables include a comprehensive quality control (QC) report to ensure data reliability.

Image
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Flexible Bioinformatics Solutions

Optional bioinformatics analysis services are available upon request to support downstream interpretation and discovery, tailored to your research needs.

Image
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1/1
High-Quality Raw Sequencing Data

Receive high-quality raw sequencing data in FASTQ format. For lane sequencing or flowcell sequencing orders, BCL-format data are also available. All deliverables include a comprehensive quality control (QC) report to ensure data reliability.

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Flexible Bioinformatics Solutions

Optional bioinformatics analysis services are available upon request to support downstream interpretation and discovery, tailored to your research needs.

More Services

Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
mRNA Sequencing
(mRNA Sequencing)
mRNA Sequencing
(mRNA Sequencing)
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Single Cell Gene Expression
(Single Cell Gene Expression)
Single Cell Gene Expression
(Single Cell Gene Expression)

More Services

Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
mRNA Sequencing
(mRNA Sequencing)
mRNA Sequencing
(mRNA Sequencing)
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Single Cell Gene Expression
(Single Cell Gene Expression)
Single Cell Gene Expression
(Single Cell Gene Expression)
Background
Background

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Sequencing Only on Illumina Sequencer

High-quality short-read sequencing of customer-prepared libraries on the Illumina platform to support diverse genomic and transcriptomic applications.
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(Sequencing Only on Illumina Sequencer)
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(Sequencing Only on Illumina Sequencer)
OverviewOverview
BenefitsBenefits
ApplicationsApplications
SpecificationsSpecifications
ResourcesResources

Novogene provides cost-effective sequencing-only services for customer-prepared, ready-to-sequence libraries on the NovaSeq platform series, including NovaSeq X Plus and NovaSeq 6000.


With a flexible range of sequencing solutions, we offer multiple read length options, scalable throughput configurations, and efficient turnaround times to support the diverse needs of research projects.


Supported by an experienced technical and operations team, Novogene combines solid scientific expertise, strict quality control standards, extensive project experience, and streamlined workflows to deliver reliable, efficient sequencing services - providing consistent data quality and dependable support throughout the entire project lifecycle.

Why Choose Illumina Seq-Only Services with Novogene?

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Why Choose Illumina Seq-Only Services with Novogene?

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Cost Efficiency
Cost Efficiency

Take advantage of industry-leading sequencing costs on a per-read or per-Gb basis, with consistently high Q30 performance.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Trusted Expertise
Trusted Expertise

Rely on Novogene’s experienced team to support you at every stage of sample processing, ensuring consistent, reliable, and high-quality results.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Rapid Turnaround Time
Rapid Turnaround Time

Benefit from our fastest turnaround times at no additional cost, with accelerated processing from quality control to data delivery, helping you meet project deadlines efficiently.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Flexible Project Options
Flexible Project Options

Maintain full control over your sequencing projects with flexible options, including multiple lane or data volume purchases, broad compatibility with diverse library types, and customizable sequencing parameters.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Dedicated Localized Support
Dedicated Localized Support

Supported by regional technical teams and local laboratories, Novogene delivers personalized and responsive services.

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Automated Workflow
Automated Workflow

Streamline project management using Novogene’s Customer Service System (CSS).

Applications of Pre-made Library Sequencing

Novogene’s pre-made library sequencing services offer a flexible and cost-effective solution for research teams with established library preparation workflows.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Applications of Pre-made Library Sequencing

Novogene’s pre-made library sequencing services offer a flexible and cost-effective solution for research teams with established library preparation workflows.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Preserve Proven Workflows

Seamlessly continue validated library preparation protocols while achieving consistent, high-quality sequencing results.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Scale Large and High-Throughput Projects

Support population studies, clinical research, and large cohort analyses with scalable sequencing capacity and optimized costs.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Enable Custom Bioinformatics Pipelines

Receive high-quality raw data (FASTQ or BCL) for direct integration into in-house bioinformatics workflows.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Support Diverse Omics Applications

Applicable to genomics, transcriptomics, targeted sequencing, and other NGS-based research with flexible sequencing configurations.

Specifications

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Specifications

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sample Requirements

Sample amounts are listed for reference only. Download the Sample Requirements to learn more. For detailed information, please contact us with your customized requests.


*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

PlatformSequencing PlatformData AmountVolumeConcentration*
NovaSeq X Plus 
PE150/PE50/SE50
NovaSeq X Plus Partial
Lane Seq
X < 30 G≥ 15 µL≥ 2 ng/L, quantified by Qubit® 2.0
(Life Technologies) or ≥ 2 nmol/L
quantified by Q-PCR
30 G ≤ X < 100 G≥ 30 µL
100 G ≤ X < 375 G≥ 70 µL
NovaSeq X Plus 10BLane sequencing
(375Gb data per lane)
≥70 μL/lane (add 70 µL for each additional lane)
NovaSeq X Plus 25BLane sequencing
(1,000 Gb data per lane)
≥ 130 μL/lane (add 130 µL for each additional lane)
NovaSeq6000 PE250NovaSeq 6000 Partial Lane SeqX < 30 M reads≥ 15 µL
30 M ≤ X < 100 M reads≥ 25 µL
100 M ≤ X < 400 M reads≥ 50 µL
NovaSeq 6000 Lane SeqLane sequencing
(400 M reads per lane)
≥ 70 µL/lane (add 70 µL for each additional lane)
*Notes:High concentration samples should be diluted before delivery. Pre-made libraries should be colorless.

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Sequencing and Analysis

PlatformRead LengthData Output
NovaSeq X PlusPE150 (10B)375Gb/lane
3 Tb/flow cell
PE150 (25B)1 Tb/lane
8 Tb/flow cell
PE501.5B reads/flowcell
SE501.5B reads/flowcell
NovaSeq 6000PE250400 M pair reads/lane
800 M pair reads/flowcell

Project Workflow

For customer‑prepared libraries, Novogene performs an initial library quality assessment to ensure they meet sequencing requirements. Qualified libraries are then pooled based on effective concentration and requested data volume and loaded onto Illumina sequencers for high‑throughput sequencing.

Project Workflow

Project Deliverables

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High-Quality Raw Sequencing Data

Receive high-quality raw sequencing data in FASTQ format. For lane sequencing or flowcell sequencing orders, BCL-format data are also available. All deliverables include a comprehensive quality control (QC) report to ensure data reliability.

Image
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1/1
Flexible Bioinformatics Solutions

Optional bioinformatics analysis services are available upon request to support downstream interpretation and discovery, tailored to your research needs.

Project Deliverables

Image
Image
1/1
High-Quality Raw Sequencing Data

Receive high-quality raw sequencing data in FASTQ format. For lane sequencing or flowcell sequencing orders, BCL-format data are also available. All deliverables include a comprehensive quality control (QC) report to ensure data reliability.

Image
Image
1/1
Flexible Bioinformatics Solutions

Optional bioinformatics analysis services are available upon request to support downstream interpretation and discovery, tailored to your research needs.

Image
Image
1/1
High-Quality Raw Sequencing Data

Receive high-quality raw sequencing data in FASTQ format. For lane sequencing or flowcell sequencing orders, BCL-format data are also available. All deliverables include a comprehensive quality control (QC) report to ensure data reliability.

Image
Image
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Flexible Bioinformatics Solutions

Optional bioinformatics analysis services are available upon request to support downstream interpretation and discovery, tailored to your research needs.

More Services

Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
mRNA Sequencing
(mRNA Sequencing)
mRNA Sequencing
(mRNA Sequencing)
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Single Cell Gene Expression
(Single Cell Gene Expression)
Single Cell Gene Expression
(Single Cell Gene Expression)

More Services

Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
Human Whole Genome Sequencing
(Human Whole Genome Sequencing)
mRNA Sequencing
(mRNA Sequencing)
mRNA Sequencing
(mRNA Sequencing)
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Whole Genome Bisulfite Sequencing (WGBS)
(Whole Genome Bisulfite Sequencing (WGBS))
Single Cell Gene Expression
(Single Cell Gene Expression)
Single Cell Gene Expression
(Single Cell Gene Expression)
Background
Background

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