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 Epigenomics Services

Discover the epigenetic mechanisms driving gene regulation and disease.
Talk to Our Team
(Our Epigenomics Services)
Talk to Our Team
(Our Epigenomics Services)

Explore Our Epigenomics Solutions

Epigenomics explores how chemical modifications to DNA, RNA, and chromatin regulate gene expression without altering the DNA sequence. From DNA methylation and chromatin accessibility to protein-DNA and RNA-protein interactions, our comprehensive epigenomics solutions help researchers uncover the regulatory mechanisms underlying development, disease, and cellular function. Explore the services below to identify the most appropriate epigenomics workflow for your research.

Explore Our Epigenomics Solutions

Epigenomics explores how chemical modifications to DNA, RNA, and chromatin regulate gene expression without altering the DNA sequence. From DNA methylation and chromatin accessibility to protein-DNA and RNA-protein interactions, our comprehensive epigenomics solutions help researchers uncover the regulatory mechanisms underlying development, disease, and cellular function. Explore the services below to identify the most appropriate epigenomics workflow for your research.

WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)
WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)

Why Researchers Choose Novogene

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Why Researchers Choose Novogene

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Platforms

Image
Image
1/1
NovaSeq X Plus
High-throughput short-read epigenomics sequencing.
Supports diverse epigenomics workflows.
Scalable epigenome profiling.

Platforms

Image
Image
1/1
NovaSeq X Plus
High-throughput short-read epigenomics sequencing.
Supports diverse epigenomics workflows.
Scalable epigenome profiling.
Background
Background

Not sure which Epigenomics solution is right for your project?

Talk to our specialist to find the right solution.

 
 
 
 
 
 
 
 
 
 
Privacy PolicyCookie PolicyCareers
banner laptop bg
banner mobile bg

Our Epigenomics Services

Discover the epigenetic mechanisms driving gene regulation and disease.
Talk to Our Team
(Our Epigenomics Services)
Talk to Our Team
(Our Epigenomics Services)

Explore Our Epigenomics Solutions

Epigenomics explores how chemical modifications to DNA, RNA, and chromatin regulate gene expression without altering the DNA sequence. From DNA methylation and chromatin accessibility to protein-DNA and RNA-protein interactions, our comprehensive epigenomics solutions help researchers uncover the regulatory mechanisms underlying development, disease, and cellular function. Explore the services below to identify the most appropriate epigenomics workflow for your research.

Explore Our Epigenomics Solutions

Epigenomics explores how chemical modifications to DNA, RNA, and chromatin regulate gene expression without altering the DNA sequence. From DNA methylation and chromatin accessibility to protein-DNA and RNA-protein interactions, our comprehensive epigenomics solutions help researchers uncover the regulatory mechanisms underlying development, disease, and cellular function. Explore the services below to identify the most appropriate epigenomics workflow for your research.

WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)
WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
WGBS

Profile genome-wide DNA methylation at single-base resolution to investigate epigenetic regulation, disease mechanisms, and development.

View Service
(WGBS)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
DM-Seq

Profile DNA methylation across targeted genomic regions with high resolution, enabling focused and cost-effective epigenetic analysis.

View Service
(DM-Seq)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
RRBS

Profile CpG-rich regions to identify DNA methylation changes associated with gene regulation, disease, and biomarker discovery.

View Service
(RRBS)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
ChIP-Seq

Map transcription factor binding and histone modifications to understand chromatin regulation and gene expression.

View Service
(ChIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
RIP-Seq

Characterise RNA-protein interactions to investigate post-transcriptional regulation and RNA-binding protein function.


View Service
(RIP-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)
ATAC-Seq

Profile chromatin accessibility to identify regulatory elements, transcription factor binding sites, and active gene regulatory regions.

View Service
(ATAC-Seq)

Why Researchers Choose Novogene

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Why Researchers Choose Novogene

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

Comprehensive Epigenomics Portfolio

Access comprehensive DNA methylation, chromatin accessibility, and epigenetic profiling solutions through one trusted partner.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

End-to-End Project Support

One partner for your entire epigenomics workflow, supported by expert scientific guidance at every stage.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Multi-omics Integration

Seamlessly integrate epigenomics data with other multi-omics technologies through one trusted partner.

Platforms

Image
Image
1/1
NovaSeq X Plus
High-throughput short-read epigenomics sequencing.
Supports diverse epigenomics workflows.
Scalable epigenome profiling.

Platforms

Image
Image
1/1
NovaSeq X Plus
High-throughput short-read epigenomics sequencing.
Supports diverse epigenomics workflows.
Scalable epigenome profiling.
Background
Background

Not sure which Epigenomics solution is right for your project?

Talk to our specialist to find the right solution.

 
 
 
 
 
 
 
 
 
 
Privacy PolicyCookie PolicyCareers