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
About UsOur LocationsOur PlatformsNewsCareersContact Us
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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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Our Genomics Services

Comprehensive genomics solutions to support discovery across human, plant, animal, and microbial research.
Talk to Our Team
(Our Genomics Services)
Talk to Our Team
(Our Genomics Services)

Find the Right Genomics Sequencing Solution

Whether you're investigating disease biology, agricultural traits, biodiversity, or microbial communities, our genomics services provide the sequencing technologies and bioinformatics expertise needed to support a wide range of research applications. Explore the solutions below to find the approach best suited to your project.

Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)

Find the Right Genomics Sequencing Solution

Whether you're investigating disease biology, agricultural traits, biodiversity, or microbial communities, our genomics services provide the sequencing technologies and bioinformatics expertise needed to support a wide range of research applications. Explore the solutions below to find the approach best suited to your project.

Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)

Why Researchers Choose Novogene

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Why Researchers Choose Novogene

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Platforms

Image
Image
1/1
NovaSeq X Plus

High-throughput sequencing for large-scale genomics studies.

Read length: 2 × 150 bp.
Up to 8 Tb output per flow cell.
Ideal for WGS, WES, RNA-Seq, and population-scale studies.
Image
Image
1/1
Nanopore PromethION & P2i

Ultra-long read sequencing for complex genome analysis.

Read lengths up to 2 Mb.
Ideal for genome assembly and methylation analysis.
Image
Image
1/1
PacBio Revio

Highly accurate long-read sequencing for genome characterization.

HiFi reads with >90% bases at Q30.
Ideal for genome assembly and structural variants.

Platforms

Image
Image
1/1
NovaSeq X Plus

High-throughput sequencing for large-scale genomics studies.

Read length: 2 × 150 bp.
Up to 8 Tb output per flow cell.
Ideal for WGS, WES, RNA-Seq, and population-scale studies.
Image
Image
1/1
Nanopore PromethION & P2i

Ultra-long read sequencing for complex genome analysis.

Read lengths up to 2 Mb.
Ideal for genome assembly and methylation analysis.
Image
Image
1/1
PacBio Revio

Highly accurate long-read sequencing for genome characterization.

HiFi reads with >90% bases at Q30.
Ideal for genome assembly and structural variants.
Image
Image
1/1
NovaSeq X Plus

High-throughput sequencing for large-scale genomics studies.

Read length: 2 × 150 bp.
Up to 8 Tb output per flow cell.
Ideal for WGS, WES, RNA-Seq, and population-scale studies.
Image
Image
1/1
Nanopore PromethION & P2i

Ultra-long read sequencing for complex genome analysis.

Read lengths up to 2 Mb.
Ideal for genome assembly and methylation analysis.
Image
Image
1/1
PacBio Revio

Highly accurate long-read sequencing for genome characterization.

HiFi reads with >90% bases at Q30.
Ideal for genome assembly and structural variants.
Background
Background

Not sure which Genomics approach is right for your project?

Talk to our specialist to find the right solution.

 
 
 
 
 
 
 
 
 
 
Privacy PolicyCookie PolicyCareers
banner laptop bg
banner mobile bg

Our Genomics Services

Comprehensive genomics solutions to support discovery across human, plant, animal, and microbial research.
Talk to Our Team
(Our Genomics Services)
Talk to Our Team
(Our Genomics Services)

Find the Right Genomics Sequencing Solution

Whether you're investigating disease biology, agricultural traits, biodiversity, or microbial communities, our genomics services provide the sequencing technologies and bioinformatics expertise needed to support a wide range of research applications. Explore the solutions below to find the approach best suited to your project.

Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)

Find the Right Genomics Sequencing Solution

Whether you're investigating disease biology, agricultural traits, biodiversity, or microbial communities, our genomics services provide the sequencing technologies and bioinformatics expertise needed to support a wide range of research applications. Explore the solutions below to find the approach best suited to your project.

Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Genome Sequencing

Sequence the complete genome to identify genetic variation, structural variants, and other genomic features. From rare disease studies to population-scale genomics, our scalable WGS workflows combine extensive sequencing capacity with comprehensive bioinformatics support.

Explore
(Whole Genome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
Whole Exome Sequencing

Target protein-coding regions to efficiently identify disease-associated variants. Choose from flexible probe and library preparation options from Agilent, Twist, and IDT, together with custom panel design, DNA extraction, and comprehensive bioinformatics support.

View Service
(Whole Exome Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
De Novo Sequencing

Generate high-quality reference genomes for novel and non-model organisms. Supported by extensive experience in complex de novo genome projects, our integrated sequencing and bioinformatics workflows deliver accurate genome assemblies and annotations across diverse plant, animal, and microbial species.

Explore
(De Novo Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)
Metagenome Sequencing

Explore microbial diversity and function using 16S/18S/ITS amplicon or shotgun metagenomic sequencing. Our end-to-end workflows support human, animal, and environmental samples, delivering comprehensive taxonomic profiling, functional annotation, and integrated bioinformatics analysis.

Explore
(Metagenome Sequencing)

Why Researchers Choose Novogene

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Why Researchers Choose Novogene

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Multi-Platform Technologies

Access a comprehensive portfolio of genomics technologies and platforms through a single trusted partner.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Local Expertise. Global Capabilities.

Responsive local support with access to global technologies and expertise.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Consultative Scientific Support

We work alongside researchers to help maximize the value of every project.

Platforms

Image
Image
1/1
NovaSeq X Plus

High-throughput sequencing for large-scale genomics studies.

Read length: 2 × 150 bp.
Up to 8 Tb output per flow cell.
Ideal for WGS, WES, RNA-Seq, and population-scale studies.
Image
Image
1/1
Nanopore PromethION & P2i

Ultra-long read sequencing for complex genome analysis.

Read lengths up to 2 Mb.
Ideal for genome assembly and methylation analysis.
Image
Image
1/1
PacBio Revio

Highly accurate long-read sequencing for genome characterization.

HiFi reads with >90% bases at Q30.
Ideal for genome assembly and structural variants.

Platforms

Image
Image
1/1
NovaSeq X Plus

High-throughput sequencing for large-scale genomics studies.

Read length: 2 × 150 bp.
Up to 8 Tb output per flow cell.
Ideal for WGS, WES, RNA-Seq, and population-scale studies.
Image
Image
1/1
Nanopore PromethION & P2i

Ultra-long read sequencing for complex genome analysis.

Read lengths up to 2 Mb.
Ideal for genome assembly and methylation analysis.
Image
Image
1/1
PacBio Revio

Highly accurate long-read sequencing for genome characterization.

HiFi reads with >90% bases at Q30.
Ideal for genome assembly and structural variants.
Image
Image
1/1
NovaSeq X Plus

High-throughput sequencing for large-scale genomics studies.

Read length: 2 × 150 bp.
Up to 8 Tb output per flow cell.
Ideal for WGS, WES, RNA-Seq, and population-scale studies.
Image
Image
1/1
Nanopore PromethION & P2i

Ultra-long read sequencing for complex genome analysis.

Read lengths up to 2 Mb.
Ideal for genome assembly and methylation analysis.
Image
Image
1/1
PacBio Revio

Highly accurate long-read sequencing for genome characterization.

HiFi reads with >90% bases at Q30.
Ideal for genome assembly and structural variants.
Background
Background

Not sure which Genomics approach is right for your project?

Talk to our specialist to find the right solution.

 
 
 
 
 
 
 
 
 
 
Privacy PolicyCookie PolicyCareers