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Novogene Europe
  • Novogene Europe
  • Genomics
    • Human Whole Genome Sequencing
    • Whole Exome Sequencing
    • Plant and Animal Whole Genome Sequencing
    • Plant and Animal De novo Sequencing
    • Microbial Whole Genome Sequencing
    • Microbial De novo Sequencing
    • Whole Plasmid SequencingOrder Online!
    Proteomics
    • Olink ProteomicsNew!
    Epigenomics
    • DNA Methylation SequencingUpdated!
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    Metabolomics
    • Untargeted MetabolomicsComing Soon!
    Transcriptomics
    • mRNA Sequencing
    • Small RNA Sequencing (sRNA‑seq)
    • Circular RNA Sequencing (circRNA-seq)
    • Total RNA Sequencing
    • Whole Transcriptome Sequencing
    • Full-Length Transcriptome Sequencing
    • Prokaryotic RNA Sequencing
    • Metatranscriptome Sequencing
    Metagenomics
    • Amplicon SequencingOrder Online!
    • Shotgun Metagenomics Sequencing
    Single Cell & Spatial Omics
    • 10X Single Cell Gene Expression
    • 10X Single Cell Immune Profiling
    • 10X Visium HD Spatial Gene Expression
    Premade Library
    • Sequencing Only on Illumina® Sequencer
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    • Accredited & Validated Clinical Research Sequencing
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    • Cancer Research
    • Immuno-oncology
    • Agrigenomics
    • Environment
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    • Drug Discovery and Development
    • Rare and Complex Diseases
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  • Contact UsContact Us
    • Amplicon Sequencing
    • Whole Plasmid Sequencing

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Human Whole Genome SequencingWhole Exome SequencingPlant and Animal Whole Genome SequencingPlant and Animal De novo SequencingDNA Methylation SequencingmRNA SequencingFull-Length Transcriptome SequencingWhole Transcriptome SequencingMetatranscriptome SequencingShotgun Metagenomics SequencingAmplicon SequencingWhole Plasmid Sequencing10X Single Cell Gene Expression10X Single Cell Immune Profiling10X Visium HD Spatial Gene ExpressionOlink ProteomicsUntargeted MetabolomicsAccredited & Validated Clinical Research Sequencing
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Copyright © 2026 Novogene Inc. All rights reserved.For Research Use Only. Not for Clinical Diagnostic Use.
    • Cart
    • Quote
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    • Cart
    • Quote
    • Enquiry
Novogene Europe
  • Novogene Europe
  • Genomics
    • Human Whole Genome Sequencing
    • Whole Exome Sequencing
    • Plant and Animal Whole Genome Sequencing
    • Plant and Animal De novo Sequencing
    • Microbial Whole Genome Sequencing
    • Microbial De novo Sequencing
    • Whole Plasmid SequencingOrder Online!
    Proteomics
    • Olink ProteomicsNew!
    Epigenomics
    • DNA Methylation SequencingUpdated!
    • Chromatin Immunoprecipitation Sequencing (ChIP-seq)
    • RNA Immunoprecipitation Sequencing (RIP-seq)
    Metabolomics
    • Untargeted MetabolomicsComing Soon!
    Transcriptomics
    • mRNA Sequencing
    • Small RNA Sequencing (sRNA‑seq)
    • Circular RNA Sequencing (circRNA-seq)
    • Total RNA Sequencing
    • Whole Transcriptome Sequencing
    • Full-Length Transcriptome Sequencing
    • Prokaryotic RNA Sequencing
    • Metatranscriptome Sequencing
    Metagenomics
    • Amplicon SequencingOrder Online!
    • Shotgun Metagenomics Sequencing
    Single Cell & Spatial Omics
    • 10X Single Cell Gene Expression
    • 10X Single Cell Immune Profiling
    • 10X Visium HD Spatial Gene Expression
    Premade Library
    • Sequencing Only on Illumina® Sequencer
    • Sequencing Only on Element SequencerNew!
    • Sequencing Only on PacBio Sequencer
    Translational Research
    • Accredited & Validated Clinical Research Sequencing
  • PromotionsPromotions
    • Platforms
    • Automated Delivery Platform (Falcon)
    • Bioinformatics Analysis Tool (NovoMagic)
    • Customer Service System (CSS)
    • Customer Support
    • Webinars
    • Case Study
    • Blog
    • Brochure
    • Cancer Research
    • Immuno-oncology
    • Agrigenomics
    • Environment
    • Food Science
    • Human Microbiome
    • Plant and Animal Microbiome
    • Drug Discovery and Development
    • Rare and Complex Diseases
    • About Us
    • News & Events
    • Careers
    • Our Locations
  • Contact UsContact Us
    • Amplicon Sequencing
    • Whole Plasmid Sequencing

ServicesServices menu

ResourcesResources menu

SupportSupport menu

CompanyCompany menu

Services
Human Whole Genome SequencingWhole Exome SequencingPlant and Animal Whole Genome SequencingPlant and Animal De novo SequencingDNA Methylation SequencingmRNA SequencingFull-Length Transcriptome SequencingWhole Transcriptome SequencingMetatranscriptome SequencingShotgun Metagenomics SequencingAmplicon SequencingWhole Plasmid Sequencing10X Single Cell Gene Expression10X Single Cell Immune Profiling10X Visium HD Spatial Gene ExpressionOlink ProteomicsUntargeted MetabolomicsAccredited & Validated Clinical Research Sequencing
Resources
WebinarsCase StudyBlogBrochure
Support
PlatformBioinformatics Analysis Tool (NovoMagic)Customer Service System (CSS)Customer Support
Company
About UsNews & EventsLocationContact Us
LinkedInLinkedIn hoverYouTubeYouTube hoverInstagramInstagram hoverXX hover
Copyright © 2026 Novogene Inc. All rights reserved.For Research Use Only. Not for Clinical Diagnostic Use.
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Chromatin Immunoprecipitation Sequencing (ChIP-seq)

Genome-wide profiling of protein-DNA interactions and histone modifications to reveal transcriptional regulation and epigenetic mechanisms.
OverviewOverview
BenefitsBenefits
ApplicationsApplications
SpecificationsSpecifications
ResourcesResources

Chromatin immunoprecipitation sequencing (ChIP-seq) enables genome-wide analysis of protein-DNA interactions and histone modification patterns. By combining chromatin immunoprecipitation with high-throughput sequencing, ChIP-seq helps researchers identify transcription factor binding sites, regulatory regions and chromatin-associated changes.


Novogene Europe supports ChIP-seq projects with sequencing and bioinformatics workflows for peak calling, motif analysis, peak annotation and functional interpretation. ChIP-seq data can also be integrated with RNA-seq, ATAC-seq or other omics data to explore gene regulation and epigenetic mechanisms across cell types, tissues or experimental conditions.

Service Highlights

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Service Highlights

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Applications

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Applications

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Specifications

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Specifications

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Resources

Example Analysis Output

Image
Image
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Peak Annotation Distribution

Summarise ChIP-seq peak distribution across promoters, exons, introns and intergenic regions.

Image
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Pathway Enrichment Analysis

Identify enriched pathways associated with peak-linked genes for functional interpretation.

Image
Image
1/1
Motif Enrichment Analysis

Detect enriched DNA sequence motifs within peak regions to explore potential transcription factor binding patterns.

Image
Image
1/1
Peak Annotation Distribution

Summarise ChIP-seq peak distribution across promoters, exons, introns and intergenic regions.

Image
Image
1/1
Pathway Enrichment Analysis

Identify enriched pathways associated with peak-linked genes for functional interpretation.

Image
Image
1/1
Motif Enrichment Analysis

Detect enriched DNA sequence motifs within peak regions to explore potential transcription factor binding patterns.

Image
Image
1/1
Peak Annotation Distribution

Summarise ChIP-seq peak distribution across promoters, exons, introns and intergenic regions.

Image
Image
1/1
Pathway Enrichment Analysis

Identify enriched pathways associated with peak-linked genes for functional interpretation.

Image
Image
1/1
Motif Enrichment Analysis

Detect enriched DNA sequence motifs within peak regions to explore potential transcription factor binding patterns.

Webinars

Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)
Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)
Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)
Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)

Explore Epigenomics Insights

Access webinars, brochures and case studies covering sequencing technologies, study planning and data interpretation.
View Webinar Library
(Explore Epigenomics Insights)
View Webinar Library
(Explore Epigenomics Insights)
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Chromatin Immunoprecipitation Sequencing (ChIP-seq)

Genome-wide profiling of protein-DNA interactions and histone modifications to reveal transcriptional regulation and epigenetic mechanisms.
OverviewOverview
BenefitsBenefits
ApplicationsApplications
SpecificationsSpecifications
ResourcesResources

Chromatin immunoprecipitation sequencing (ChIP-seq) enables genome-wide analysis of protein-DNA interactions and histone modification patterns. By combining chromatin immunoprecipitation with high-throughput sequencing, ChIP-seq helps researchers identify transcription factor binding sites, regulatory regions and chromatin-associated changes.


Novogene Europe supports ChIP-seq projects with sequencing and bioinformatics workflows for peak calling, motif analysis, peak annotation and functional interpretation. ChIP-seq data can also be integrated with RNA-seq, ATAC-seq or other omics data to explore gene regulation and epigenetic mechanisms across cell types, tissues or experimental conditions.

Service Highlights

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Service Highlights

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Targeted Chromatin Enrichment
Targeted Chromatin Enrichment

ChIP-seq enriches DNA regions associated with specific transcription factors, histone modifications or chromatin-binding proteins for genome-wide analysis.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Genome-wide Peak Detection
Genome-wide Peak Detection

Sequencing and peak calling workflows help identify enriched genomic regions, supporting analysis of binding sites and chromatin-associated regulatory elements.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Motif and Peak Annotation
Motif and Peak Annotation

Bioinformatics analysis can support motif discovery, peak annotation and functional interpretation to help connect binding patterns with biological context.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Multi-omics Integration
Multi-omics Integration

ChIP-seq data can be integrated with RNA-seq, ATAC-seq or other omics datasets to explore gene regulation and epigenetic mechanisms.

Applications

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Applications

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Transcription Factor Binding

ChIP-seq helps identify genome-wide binding sites for transcription factors, supporting studies of gene regulation and regulatory network activity.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Histone Modification Profiling

Profile histone marks associated with active, repressed or poised chromatin states to investigate epigenetic regulation across samples or conditions.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Regulatory Element Discovery

Identify promoters, enhancers and other regulatory regions associated with protein-DNA interactions or histone modification patterns.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Disease and Cell State Research

ChIP-seq supports studies of chromatin changes linked to development, disease mechanisms, treatment response and cell-type-specific regulation.

Specifications

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Specifications

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sample Requirements

The quantities listed are provided for reference only. Please download the Sample Requirements for detailed guidance, or contact us to discuss your project-specific requirements.

Sample TypeRequired AmountFragment sizePurity
Enriched DNA Sample≥ 5 ng (Concentration ≥ 0.5 ng/μL)100 bp~500 bpA260/280=1.8-2.0

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Sequencing and Analysis

Recommended data outputs and analysis examples are provided for reference only. For detailed information, please contact us to discuss your project-specific analysis requirements.

PlatformIllumina Xplus
Read LengthPair-end 150 bp
Sequencing Depth≥ 20 million read pairs per sample for the species with reference genome
Standard Data AnalysisData Quality Control
Mapping onto reference genome
Fragment size prediction
Peak calling
Motif analysis
Peak annotation and functional analysis of peak-associated genes
Summary of differential peaks and functional analysis of differential peak related genes

Resources

Example Analysis Output

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Peak Annotation Distribution

Summarise ChIP-seq peak distribution across promoters, exons, introns and intergenic regions.

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Pathway Enrichment Analysis

Identify enriched pathways associated with peak-linked genes for functional interpretation.

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Motif Enrichment Analysis

Detect enriched DNA sequence motifs within peak regions to explore potential transcription factor binding patterns.

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Peak Annotation Distribution

Summarise ChIP-seq peak distribution across promoters, exons, introns and intergenic regions.

Image
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1/1
Pathway Enrichment Analysis

Identify enriched pathways associated with peak-linked genes for functional interpretation.

Image
Image
1/1
Motif Enrichment Analysis

Detect enriched DNA sequence motifs within peak regions to explore potential transcription factor binding patterns.

Image
Image
1/1
Peak Annotation Distribution

Summarise ChIP-seq peak distribution across promoters, exons, introns and intergenic regions.

Image
Image
1/1
Pathway Enrichment Analysis

Identify enriched pathways associated with peak-linked genes for functional interpretation.

Image
Image
1/1
Motif Enrichment Analysis

Detect enriched DNA sequence motifs within peak regions to explore potential transcription factor binding patterns.

Webinars

Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)
Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)
Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)
Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research

Explore the latest NGS-based approaches for epigenetics research, including WGBS, EM-seq, ChIP-seq, RIP-seq, and ATAC-seq. This webinar will cover the principles, applications, workflows, and bioinformatics strategies used to investigate DNA methylation, chromatin accessibility, and gene regulation.

Learn More
(Epigenetics Elevated: NGS Solutions for Transformative Epigenetics Research)

Explore Epigenomics Insights

Access webinars, brochures and case studies covering sequencing technologies, study planning and data interpretation.
View Webinar Library
(Explore Epigenomics Insights)
View Webinar Library
(Explore Epigenomics Insights)
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