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
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    • Automated Delivery Platform (Falcon)
    • Bioinformatics Analysis Tool (NovoMagic)
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    • 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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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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Microbial Whole Genome Sequencing

Comprehensive whole-genome sequencing of microorganisms to characterize genetic variation, genome structure, and functional potential.
Request a Quote
(Microbial Whole Genome Sequencing)
Request a Quote
(Microbial Whole Genome Sequencing)
OverviewOverview
BenefitsBenefits
ApplicationsApplications
SpecificationsSpecifications
ResourcesResources

Microbial Whole Genome Sequencing (mWGS) is an advanced and efficient method for analyzing entire microbial genomes, including bacteria and viruses, to generate accurate reference genomes, identify microbes, and support various comparative genomic studies. Unlike traditional PCR, mWGS eliminates labor-intensive cloning and mapping, making it quicker and more cost-effective.


At Novogene, our high-throughput sequencing technology enables faster microbial identification, supporting a wide range of research applications.

Why Choose Novogene for mWGS? What we offer?

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

Why Choose Novogene for mWGS? What we offer?

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

Applications of Microbial Whole Genome Sequencing

Unlock deep insights into microbial genetics and evolution with whole genome sequencing applications.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

Applications of Microbial Whole Genome Sequencing

Unlock deep insights into microbial genetics and evolution with whole genome sequencing applications.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Demo Results

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1/1
Mutation Spectrum

Compare mutation type proportions across samples to review overall sequence variation patterns.

Image
Image
1/1
COG Functional Classification

Summarise predicted gene functions by COG category to support functional genome interpretation.

Image
Image
1/1
Coding Variant Effects

Summarise coding-region variant effects, including synonymous, non-synonymous and stop-gain or stop-loss changes.

Demo Results

Image
Image
1/1
Mutation Spectrum

Compare mutation type proportions across samples to review overall sequence variation patterns.

Image
Image
1/1
COG Functional Classification

Summarise predicted gene functions by COG category to support functional genome interpretation.

Image
Image
1/1
Coding Variant Effects

Summarise coding-region variant effects, including synonymous, non-synonymous and stop-gain or stop-loss changes.

Image
Image
1/1
Mutation Spectrum

Compare mutation type proportions across samples to review overall sequence variation patterns.

Image
Image
1/1
COG Functional Classification

Summarise predicted gene functions by COG category to support functional genome interpretation.

Image
Image
1/1
Coding Variant Effects

Summarise coding-region variant effects, including synonymous, non-synonymous and stop-gain or stop-loss changes.

More Services

Microbial De novo Sequencing
(Microbial De novo Sequencing)
Microbial De novo Sequencing
(Microbial De novo Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)

More Services

Microbial De novo Sequencing
(Microbial De novo Sequencing)
Microbial De novo Sequencing
(Microbial De novo Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)
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Microbial Whole Genome Sequencing

Comprehensive whole-genome sequencing of microorganisms to characterize genetic variation, genome structure, and functional potential.
Request a Quote
(Microbial Whole Genome Sequencing)
Request a Quote
(Microbial Whole Genome Sequencing)
OverviewOverview
BenefitsBenefits
ApplicationsApplications
SpecificationsSpecifications
ResourcesResources

Microbial Whole Genome Sequencing (mWGS) is an advanced and efficient method for analyzing entire microbial genomes, including bacteria and viruses, to generate accurate reference genomes, identify microbes, and support various comparative genomic studies. Unlike traditional PCR, mWGS eliminates labor-intensive cloning and mapping, making it quicker and more cost-effective.


At Novogene, our high-throughput sequencing technology enables faster microbial identification, supporting a wide range of research applications.

Why Choose Novogene for mWGS? What we offer?

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

Why Choose Novogene for mWGS? What we offer?

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Fast Turnaround
Fast Turnaround

Receive high-quality sequencing data in as little as two weeks.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Comprehensive Analysis
Comprehensive Analysis

Detects mutations (SNP, InDel, CNV, SV) and studies evolution and population traits.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Localized Support
Localized Support

Regional technical teams provide personalized assistance for your unique needs.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Customizable Solutions
Customizable Solutions

Expertly designed projects for complex samples and challenging studies.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

Professional Services
Professional Services

From material selection to data analysis, every step is designed for precise results.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

High-Quality Library Preparation
High-Quality Library Preparation

Size selection ensures optimized insert size and reliable data quality.

Applications of Microbial Whole Genome Sequencing

Unlock deep insights into microbial genetics and evolution with whole genome sequencing applications.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

Applications of Microbial Whole Genome Sequencing

Unlock deep insights into microbial genetics and evolution with whole genome sequencing applications.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Detect Genetic Variations

Accurately identify genome differences by comparing sequences to reference genomes.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Interpret Genetic Traits

Link genetic variations to phenotypic traits such as virulence or benignity.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Trace Microbial Evolution

Study SNP patterns to uncover microbial origins, spread, and diversification.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

Identify Novel Species

Leverage genetic data to define and classify previously unknown microbial species cultured in labs.

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

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.

Library TypeSample TypeAmount (Qubit)VolumeConcentrationPurity
Microbial whole genome libraryGenomic DNA≥ 100 ng≥ 20 μL≥ 5 ng/μLA260/280=1.8-2.0;
no degradation,
no contamination
Microbial whole genome library
(PCR-free)
Genomic DNA≥ 1.2 μg≥ 20 μL≥ 50 ng/μL

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Sequencing and Analysis

Recommended data outputs and analysis contents displayed are for reference only. For detailed information, please contact us with your customized requests.

Platform TypeIllumina NovaSeq Platforms
Read LengthPaired-end 150 bp
Recommended Sequencing Depth≥ 100x for bacterial genomes
≥ 100x for fungal genomes
Standard Data AnalysisData quality control: filtering reads containing adapter or with low quality
Alignment with the reference genome, statistics of sequencing depth and coverage
SNP/InDel calling, annotation and statistics
CNV calling, annotation and statistics
SV calling, annotation and statistics

Project Workflow

Project Workflow

Demo Results

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Mutation Spectrum

Compare mutation type proportions across samples to review overall sequence variation patterns.

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1/1
COG Functional Classification

Summarise predicted gene functions by COG category to support functional genome interpretation.

Image
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Coding Variant Effects

Summarise coding-region variant effects, including synonymous, non-synonymous and stop-gain or stop-loss changes.

Demo Results

Image
Image
1/1
Mutation Spectrum

Compare mutation type proportions across samples to review overall sequence variation patterns.

Image
Image
1/1
COG Functional Classification

Summarise predicted gene functions by COG category to support functional genome interpretation.

Image
Image
1/1
Coding Variant Effects

Summarise coding-region variant effects, including synonymous, non-synonymous and stop-gain or stop-loss changes.

Image
Image
1/1
Mutation Spectrum

Compare mutation type proportions across samples to review overall sequence variation patterns.

Image
Image
1/1
COG Functional Classification

Summarise predicted gene functions by COG category to support functional genome interpretation.

Image
Image
1/1
Coding Variant Effects

Summarise coding-region variant effects, including synonymous, non-synonymous and stop-gain or stop-loss changes.

More Services

Microbial De novo Sequencing
(Microbial De novo Sequencing)
Microbial De novo Sequencing
(Microbial De novo Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)

More Services

Microbial De novo Sequencing
(Microbial De novo Sequencing)
Microbial De novo Sequencing
(Microbial De novo Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Shotgun Metagenomic Sequencing
(Shotgun Metagenomic Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Amplicon Sequencing
(Amplicon Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Metatranscriptome Sequencing
(Metatranscriptome Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)
Prokaryotic RNA Sequencing
(Prokaryotic RNA Sequencing)
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