Genomics and High-Throughput Sequencing Services

Genomics and transcriptomics services have revolutionized drug discovery and development by enabling researchers to better understand disease mechanisms and identify potential drug targets. To provide the highest quality genomics and transcriptomics services, we have invested in industry-leading equipment and developed automated workflows to ensure reproducible results.

Integrate our genomics services with your in vivo or in vitro studies with us, or use it as standalone service

Explore and validate drug mechanism of action with advanced genomic analysis
Identify genetics features associated with drug response through genomics profiling
Understand drug resistance by interrogating the immunogenomics of tumor-immune interactions
Take advantage of our proprietary tools and model data including our database of NGS-characterized model

Comprehensive Translational Genomics and Transcriptomics Services

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Key Advantages of Our Genomics and Transcriptomics Services

Expertise: Our team of experienced scientists, laboratory technicians, and bioinformaticians have extensive knowledge and expertise in the latest technologies and methodologies.
Customization: We work closely with our clients to understand their research needs and design customized solutions that deliver reliable and reproducible results.
Quality: We adhere to strict quality control measures throughout workflow to ensure accurate and consistent data generation.
Speed: Fast turnaround times without compromising quality.
Comprehensive capabilities: Our wide range of industry-leading equipment enables us to offer comprehensive capabilities for a variety of research needs.
Data analysis support: Our bioinformatics team provides expert data analysis and interpretation, ensuring that our clients have access to meaningful insights from their data.

Our key technology platforms include:

Next-Generation Sequencing (NGS): MGISEQ-2000 and Illumina NovaSeq 6000 sequencing platforms, for cost-efficient and high-quality sequencing data for a wide range of applications.
Long-read sequencing: PacBio third-generation sequencing, for de novo genome assembly, structural variation detection, and microbiome sequencing.
Optical genome mapping: Bionano Saphyr system, for high-resolution structural variation detection and genome assembly.
Single-cell sequencing: 10x Genomics platform, for high-throughput single-cell sequencing for transcriptomics and epigenetics analysis.
NanoString: nCounter and GeoMx platforms, for high-throughput gene expression analysis and spatial biology.

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Standard Genomics Services

Sample preparation: DNA/RNA extraction, mRNA purification, microRNA extraction, and NGS library preparation
Conventional assays: Target gene expression assay, virus copy number assay, gene copy number variation analysis, gene mutation validation, and gene fusion validation

Advanced Genomics and Next-Generation Sequencing Services

RNA-Seq, WES, WGS, WGBS, lncRNA-seq, single-cell sequencing, PacBio long read sequencing, Bionano structural variation detection, microbiome sequencing (full-length 16S sequencing, metagenomics sequencing, and metatranscriptomics sequencing), and Nanostring services

Mouse I/O RNA-Seq Panel

Get rapid transcriptomic insights into key immune cell populations, I/O pathways and processes in the tumor microenvironment by comprehensive profiling of 1080 genes from a single sample

Cell Line Authentication with Deep Sequencing

The first commercial deep sequencing-based CLA service. Significantly overperforms with increased accuracy, sensitivity, throughout, and provides more extensive information compared to conventional PCR-based STR assay.