GENESMART
NGS Sequencing Services
Are you seeking an optimal Next-Generation Sequencing (NGS) solution for your research project? GeneSmart Co., Ltd. is your answer. We provide professional NGS sequencing services, employing the most advanced sequencing technologies to cater to diverse research needs across a wide range of organisms, including viruses, bacteria, fungi, plants, and animals.
Through our rapid, efficient, and exceptionally accurate workflows, we guarantee reliable results. Your data is processed at our partner NOVOGENE’s internationally accredited laboratory in Singapore, ensuring the highest quality. Choose GeneSmart to optimize your research time and resources.
Novogene’s Genomics sequencing services are designed to meet a diverse range of your research objectives.
- Whole Genome Sequencing (WGS): Providing a comprehensive overview of the genome, WGS is a powerful tool for studies in disease research, population genetics, and evolution.
- Target Capture Sequencing (TCS): With its ability to focus deeply on exons (protein-coding regions of the genome) and specific genes of interest, TCS optimizes the efficiency of in-depth analysis, facilitating the discovery of significant genetic variations.
- De novo Sequencing: Offers a distinct advantage for plant, animal, and microbial evolution research. This service provides genome assembly and annotation capabilities for less-studied species or those lacking complete reference genomes, paving the way for new insights into biodiversity.
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16S/18S/ITS Amplicon Metagenomic Sequencing
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Shotgun Metagenomic Sequencing (short read)
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Microbial De novo Sequencing
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Animal and Plant De novo Sequencing
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Mouse Whole Exome Sequencing (mWES)
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Human Whole Exome Sequencing
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Microbial Whole Genome Sequencing
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Animal and Plant Whole Genome Sequencing
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Human Whole Genome Sequencing
NGS sequencing – Novogene offers leading sequencing solutions to explore mechanisms of gene expression regulation and molecular interactions:
Bisulfite Sequencing: Including Whole Genome Bisulfite Sequencing (WGBS) and Reduced-Representation Bisulfite Sequencing (RRBS). These services enable the detection of methylated cytosines on a genome-wide scale with single-nucleotide resolution, providing profound insights into the regulatory effects of methylation on gene function and expression.
ChIP-seq and RIP-seq Services:
- ChIP-seq (Chromatin Immunoprecipitation Sequencing): Efficiently analyzes protein-DNA interactions, helping to identify protein binding sites across the entire genome.
- RIP-seq (RNA Immunoprecipitation Sequencing): Provides in-depth analysis capabilities for RNA-protein interactions, elucidating the roles of proteins in RNA-related processes.
The groundbreaking convergence of single-cell omics and spatial omics is ushering in a new era in biomedical research, enabling the elucidation of biological complexities at both the cellular and tissue levels. This represents a key to scientific discoveries and medical innovations.
Single-Cell Sequencing
Single-cell omics refers to a collection of advanced technologies that allow scientists to study biological molecules at the resolution of individual cells. Utilizing techniques such as single-cell genomics, transcriptomics, epigenomics, proteomics, and metabolomics, we empower you to explore cellular diversity and dynamics with unprecedented precision. This technology plays an essential role in personalized medicine and in deepening our understanding of complex biological systems.
Novogene proudly offers comprehensive single-cell sequencing services, including:
- Single-cell gene expression analysis.
- Single-cell immune profiling.
- Long-read single-cell transcriptome analysis.
Spatial Omics Sequencing
Spatial omics enables researchers to map gene expression directly within the spatial architecture of tissues, preserving the context of cellular organization. Unlike conventional RNA sequencing that aggregates data from bulk tissue samples, spatial transcriptomics retains the spatial distribution of gene expression, facilitating detailed exploration of cellular interactions and tissue heterogeneity.
This technology provides profound insights into the spatial arrangement and functional states of cells within their native microenvironments, which is crucial for understanding developmental biology, pathology, and therapeutic responses.
With Novogene’s spatial omics services, we provide gene expression mapping directly within the spatial structure of tissues. This technology preserves cellular organizational context, enabling deep exploration of cellular interactions and tissue heterogeneity. It is an ideal solution for research in developmental biology, pathology, and therapeutic responses, offering profound insights into cellular organization within its native environment.
Transcriptomics provides researchers with a highly sensitive and precise method for measuring transcription across the entire genome at single-nucleotide resolution. Notably, RNA sequencing (RNA-seq) enables the comprehensive assessment of transcript levels, identification of differentially expressed genes and alternative splicing events, and the detection of single nucleotide polymorphisms (SNPs) and insertions/deletions (InDels). This makes RNA-seq an indispensable tool in modern biological research.
RNA-seq Solutions for Research
As a leader in genomics and transcriptomics services, Novogene offers a diverse range of RNA-seq solutions, including:
- Coding and Non-coding RNA Sequencing: Explore the intricate interactions between these RNA types in eukaryotic organisms.
- Whole Transcriptome Analysis: Leveraging advanced RNA-seq technologies, we help elucidate genetic regulatory mechanisms and functions.
Novogene is dedicated to supporting you in achieving your research objectives, whether you are utilizing:
- Meta-transcriptomic Sequencing Services: Facilitating the analysis of prokaryotic species at both individual and community levels.
- Iso-seq Technology: For in-depth analysis of full-length transcript isoforms.
Comprehensive RNA-seq Services
Experience the unparalleled convenience and efficiency of Novogene’s RNA-seq and transcriptomics services through our end-to-end solutions. We provide:
- Diverse Library Preparation Options: Suitable for various sample types and research goals.
- Multi-Platform Compatibility: Supported on leading sequencing platforms such as Illumina NovaSeq and PacBio long-read platforms, ensuring the highest data quality.
Furthermore, you can enhance your RNA-seq data analysis with our free-to-use bioinformatics tools available on the NovoMagic platform. These tools are specifically designed for projects like ‘Human mRNA-seq’ and ‘Plant and Animal Eukaryotic mRNA-seq with reference’, integrating the latest advancements in RNA-seq and transcriptomics.
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Metatranscriptome Sequencing
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Prokaryotic RNA Sequencing
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Direct RNA Sequencing
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Isoform Sequencing (Full-length Transcript Sequencing)
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Whole Transcriptome Sequencing
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Circular RNA Sequencing (circRNA-seq)
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Small RNA Sequencing (sRNA-seq)
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Long Non-coding RNA Sequencing (lncRNA-seq)
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mRNA Sequencing (mRNA-seq)
Novogene accepts client-prepared libraries for sequencing. We possess a Next-Generation Sequencing (NGS) platform with diverse options for read length, throughput, and turnaround time. We directly sequence client-provided libraries that meet our quality standards, generating high-quality sequencing data to provide a robust foundation for your bioinformatics analysis.
Novogene’s professional and efficient operations team ensures project progress and data quality for our clients. We strive to deliver rapid and convenient sequencing services. Our services combine scientific experimental design, rigorous quality control management, extensive project experience, and high-quality service to ensure every step is executed flawlessly, providing maximum support for scientific research.
Leveraging world-leading capabilities, including Illumina, PacBio, and Oxford Nanopore platforms, Novogene delivers exceptional results.
What is the NGS service recaption process at GeneSmart?

1. Sample Preparation Guidelines: HERE
2. Sample Packaging and Shipping Guidelines: HERE
3. Sample Requirements by Application Type: HERE
4. Sample Quality Control (QC) Guidelines
- Upon receipt, we will immediately perform Quality Control (QC) on the samples. Samples will be classified into three categories: “Pass,” “Hold,” or “Fail,” depending on sample quality and quantity.
- For samples that pass QC, library preparation will be carried out according to standard procedures. We commit to ensuring the required data yield for these samples as specified in the Customer’s Purchase Order (PO).
- Samples that do not meet QC standards will be classified as “Hold” or “Fail.” Please discuss with a Novogene representative if you wish to proceed with processing these samples.
- Please note that amplified cDNA samples and Olink samples are subject to different QC criteria.
- We recommend submitting double the required sample amount whenever possible to allow for potential library re-preparation.
- Please note that the sample volume used for QC (2 µL – 5 µL) is not included in the total sample volume required under the Sample Submission Guidelines.
5. Sample Submission Information
5.1. Submission at GeneSmart
Sample receiving time: Monday–Tuesday weekly, before 5:00 PM
Receiving address: 2nd Floor, GeneSmart Company, 65–67 Street No. 5, Ward 8, District 11, Ho Chi Minh City
Customer Service:
0784 153 953 (Ms. Dao)
0333 752 885 (Ms. Thu)
0832 388 778 (Hotline)
Email: [email protected] or [email protected]
5.2. Submission at Customer’s Site
Sample pickup time: Monday–Tuesday weekly, before 3:00 PM
Customers must package samples according to the guidelines in Section 2
A FedEx courier will contact the customer for sample pickup
6. Completion of Sample Information Confirmation Form: HERE
Note: Customers wishing to submit samples are requested to complete the confirmation form within 3 hours from the time of sample receipt to avoid delays in the GTT sample submission procedure.
7. Turnaround Time
15–20 days from the date of receiving the customer’s Sequencing Confirmation (after QC results are available).
8. Quotation Terms and Payment Method
Payment terms:
50% of the service fee via bank transfer upon sample submission
The remaining 50% within 3 days from the date of QC results and sequencing confirmation
(Please ensure timely payment to avoid delays in data delivery.)
Bank transfer details:
Account name: GENESMART SCIENCE AND TECHNOLOGY COMPANY LIMITED
Bank: Vietnam Technological and Commercial Joint Stock Bank (TECHCOMBANK) – Cho Lon Branch
Account number: 190 35975784 011
9. Terms and Conditions
9.1. A Purchase Order (PO) or payment is mandatory to initiate the project and data delivery. Please clearly state the quotation number in the PO. Once samples are submitted, any modification or cancellation must be approved in writing by GeneSmart.
9.2. For DNA/RNA short-run sequencing samples that pass internal QC criteria but generate lower data output than initially quoted, we commit to performing additional sequencing within a reasonable scope at no extra charge to meet the quoted data yield. This may extend the project timeline. However, if the data shortfall is less than 5% of the quoted amount, additional sequencing may not be performed, and the project will proceed with the existing data.
9.3. Additional demultiplexing services will be charged for premade libraries if the number of indexes exceeds the specified limit. For partial lane sequencing, demultiplexing is free for up to 10 indexes per Gb of data. For full lane sequencing, demultiplexing is free for up to 100 indexes per lane. Additional fees will apply if these limits are exceeded.
9.4. All samples submitted to Novogene will be destroyed 60 days after final result delivery. Any samples stored at Novogene for more than 6 months without processing (library preparation/sequencing) will also be destroyed.
9.5. All data will be deleted 30 days after data delivery. Additional charges will apply if customers request data storage beyond 30 days. Please contact your consultant for extended storage options.
9.6. Upon project completion, an invoice will be issued based on the services performed. Additional costs may arise if the information provided is inaccurate or incomplete.
9.7. We reserve the right to suspend data delivery or cancel orders if payment is not made on time.
9.8. Pricing information is CONFIDENTIAL and may only be shared with parties directly involved in the project. Customers agree to keep confidential all non-public technical information or instructions (including gene sequences, oligo types, or sequences) provided during discussions or negotiations related to our products or services.
9.9. GeneSmart reserves the right to revise quotations if the project scope changes. In such cases, we are not obligated to continue the project unless both parties agree to the revised quotation terms.
9.10. Customers are solely responsible for ensuring that the use of generated data complies with all applicable laws, regulations, and policies of relevant authorities. Customers must obtain all necessary approvals and permissions prior to sample submission and bear full responsibility for ensuring the data is suitable for its intended use.
Why Partner with GeneSmart ?
Next-Generation Sequencing (NGS) is a revolutionary technology for efficient DNA decoding, generating precise signals from the growing nucleotide chain.
At GeneSmart, we offer comprehensive Next-Generation Sequencing (NGS) services, from sample extraction, library preparation, and sequencing to in-depth bioinformatics analysis. Our NGS services are performed at the state-of-the-art laboratory of our strategic partner, Novogene in Singapore (or “at our internationally accredited partner laboratories”), ensuring that you receive the highest quality data.
Our team of Ph.D.-level scientists is committed to providing complimentary consultations, real-time updates, and dedicated post-delivery support, accompanying you through every step of your project.
As scientists and leaders in the field of genomics, we continuously optimize our processes to deliver superior results that meet your budget and deadlines. Whether this is your first or your hundredth NGS project, we are always committed to helping you find the next-generation sequencing service best suited to your specific research needs.
Next-Generation Sequencing (NGS) sample preparation and data analysis options enable a wide range of applications. For instance, NGS allows laboratories to:
- Perform rapid whole-genome sequencing
- Conduct deep sequencing of target regions
- Utilize RNA sequencing (RNA-Seq) to discover novel RNA variants, identify splice junctions, or quantify mRNA for gene expression analysis
- Analyze epigenetic factors such as genome-wide DNA methylation and DNA-protein interactions
- Sequence cancer samples to investigate rare somatic variants, tumor byproducts, and more
- Study the human microbiome
- Identify novel pathogens.
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Novogene provides comprehensive Multi-Omics solutions engineered to fully support the realization of your research objectives. Our dedicated team of experts is ready to collaborate with you at every stage, enhancing your genomics research experience — from providing in-depth technical analyses and assisting with the selection of sequencing applications and platforms, to delivering professional data analysis.
Why Partner with Novogene?
Global Multi-Platform Capabilities: Benefit from our exceptional multi-platform operational capabilities. Novogene operates 8 world-class genomics laboratories across continents, ensuring quality and efficiency for every project.
Convenient Project Management System: Manage all your sequencing projects easily and centrally on our Customer Service System (CSS). This system includes shared functionalities, making collaborative project management with your peers more convenient and efficient.
Powerful and Free RNA-seq Data Analysis Tools: Customize and re-analyze your RNA sequencing data with NovoMagic — our entirely free-to-use, cloud-based RNA-seq bioinformatics service. NovoMagic provides 17 toolkits allowing for customized data analysis, from Venn diagrams, Volcano plots, GO/KEGG enrichment, and more.
Diverse Research Support: Discover our comprehensive support for your research journey. Novogene offers proteomics services and a variety of other diverse sequencing services, continuously enhancing your research capabilities.




















