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Next Generation Sequencing

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What Problems Can Our NGS Solutions Solve?

Next-generation sequencing (NGS) has revolutionized the way researchers and biopharmaceutical companies analyze genomic and transcriptomic information. From rare variant detection to large-scale transcriptome profiling, NGS provides extremely sensitive, high-throughput analysis for a wide range of biological samples and applications.

Our NGS services are designed to support research, translational studies, and biologics development through integrated sequencing and bioinformatics workflows. We offer complete services from experimental design, sample quality evaluation, library preparation, sequencing, data analysis to reporting.

We provide multi-omics research like DNA sequencing, RNA sequencing, single cell analysis, epigenetic profiling and metagenomic characterization using modern sequencing technologies and bioinformatics driven analytic pipelines.

Whether for oncology research, cell and gene therapy development, infectious disease studies, or precision medicine applications, our team delivers reliable sequencing data tailored to project-specific objectives. Our services support both cell-based samples and biologic products through dedicated sequencing workflows and bioinformatics solutions.

Our NGS Service Capabilities

DNA Sequencing

Genomic characterization and variant profiling to support comprehensive research studies and translational applications in human, animal, and microbial systems.

  • Whole Genome Sequencing (WGS)
  • Whole Exome Sequencing (WES)
  • Targeted Resequencing & Gene Panels

RNA Sequencing

High-sensitivity transcriptomic analysis for quantitative gene expression profiling, functional pathway discovery, and transcript structure characterization.

  • Bulk RNA-Seq
  • Differential Expression Analysis (DEG)
  • Small RNA / miRNA Sequencing

Epigenetic Sequencing

Genome-wide chromatin accessibility and DNA methylation profiling to investigate gene regulation and epigenetic modifications.

  • ATAC-Seq
  • ChIP-Seq
  • Methylation Sequencing (WGBS/RRBS)

Metagenomic Sequencing

Comprehensive microbial community and pathogen profiling for taxonomic classification and functional microbiome analysis.

  • 16S/18S/ITS rRNA Sequencing
  • Shotgun Metagenomics
  • Viral Metagenomics (Adventitious Agent Detection)

Sample Types We Support

Cell Samples

Primary cells, stem cells, immune cells, engineered cell products, organoids, and established cell lines for genomic and transcriptomic analysis.

Biological Products

Viral vectors, monoclonal antibodies, vaccines, exosomes, recombinant proteins, and other biologics for characterization and quality assessment.

Our Technology Platforms

To ensure unmatched data accuracy, high throughput, and robust data integrity, our sequencing workflows utilize industry-standard, state-of-the-art platforms tailored to your specific project scale and regulatory needs.

  • Illumina NovaSeq™ Platform (Short-Read Sequencing)

The gold standard for high-throughput, high-accuracy sequencing. It is highly optimized for deep genomic profiling, RNA-Seq, and comprehensive differential expression analysis with guaranteed high Q30 scores.

  • PacBio® Revio™ System (Long-Read/HiFi Sequencing)

Utilizing High-Fidelity (HiFi) long-read technology to deliver 99.9% single-molecule accuracy. This platform is essential for characterizing complex genomic regions, structural variants, and verifying viral vector integrity (such as AAV/Lentivirus full-length sequencing).

  • 10x Genomics Chromium™ System (Single-Cell Partitioning)

The premier automated profiling platform for single-cell research. It enables high-resolution droplet partitioning for single-cell RNA-Seq, immune repertoire characterization, and mapping cell heterogeneity.

*Disclaimer: All product names, trademarks, and registered trademarks mentioned on this page are property of their respective owners. Their use here is for informational purposes only to describe our service capabilities and does not imply affiliation or endorsement.

NGS Workflow

Fig. 1: Schematic Overview of the Next-Generation Sequencing (NGS) Workflow .

Data Analysis & Quality Assurance

Advanced Bioinformatics Analysis

Our bioinformatics team provides comprehensive downstream data analysis including:

  • Variant Detection
  • Differential Gene Expression Analysis
  • Pathway Enrichment Analysis
  • Cell Clustering
  • Microbial Community Profiling
  • Data Visualization and Reporting

Rigorous Quality Assurance

Rigorous quality management measures are integrated throughout the sequencing workflow to ensure data consistency and reliability.

  • Sequencing QC metrics monitoring
  • Internal process controls
  • Library quality assessment
  • Reproducibility evaluation
  • Data integrity verification

Applications of NGS 

Our NGS services support a wide range of research and therapeutic development applications.

Oncology

Cancer genomics, mutation profiling, liquid biopsy research, and tumor heterogeneity analysis.

Cell & Gene Therapy

Vector characterization, integration analysis, immune profiling, and engineered cell evaluation.

Immunology

Immune repertoire sequencing, inflammatory pathway analysis, and immune cell profiling.

Infectious Diseases

Pathogen detection, microbial characterization, and host-pathogen interaction studies.

Stem Cell Research

Stem cell differentiation analysis, pluripotency assessment, and lineage tracing.

Precision Medicine

Biomarker discovery, genomic profiling, and patient stratification studies

Why Choose Us

  • Advanced Sequencing Platforms

Industry-standard sequencing technologies for high-quality data generation.

  • Bioinformatics Expertise

Integrated bioinformatics analysis and customized data interpretation workflows.

  • Flexible Sample Support

Compatibility with low-input, complex, and cryopreserved samples.

  • Customized Project Design

Sequencing strategies tailored to specific research and development goals.

  • Reliable Quality Control

Standardized workflows with rigorous QC monitoring throughout the project lifecycle.

  • Fast Turnaround Time

Efficient project management and streamlined sequencing workflows.

Ready to Start Your NGS Project? 

Discuss your project with our scientific team to identify the most suitable sequencing strategy for your research or development needs.

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