We offer comprehensive genomics and transcriptomics research services utilizing advanced Next Generation Sequencing (NGS) platforms. Our capabilities span whole genome and exome sequencing, RNA-Seq, and single-cell analysis, providing tailored, end-to-end solutions that include experimental design, sequencing, and bioinformatics interpretation. With rigorous quality control procedures, adaptable project workflows, and strict data confidentiality, we deliver reliable, publication-ready results to support your research objectives.
Genomics Services:
- Whole Genome Sequencing (WGS) for variant detection and genome assembly
- Whole Exome Sequencing (WES) for targeted variant identification
- Targeted gene panel sequencing
- Metagenomics for microbial community profiling
Transcriptomics Services:
- RNA-Seq for comprehensive gene expression and transcript discovery
- Single-cell RNA sequencing for high-resolution cellular characterization
- Small RNA sequencing for miRNA and non-coding RNA profiling
- Differential expression and pathway analysis
Advantages of Our NGS Services:
- Advanced Platforms: Illumina NextSeq2000, Element Biosciences Aviti, among others
- Flexible Project Design: Customized to meet individual research requirements
- Stringent Quality Control: Robust QC protocols at each project stage
- Comprehensive Bioinformatics Support: From raw data processing to biological interpretation
- Data Confidentiality & IP Protection: Secure management of all client information
Our NGS-based genomics and transcriptomics services are designed to accelerate diverse research initiatives—including population genomics, disease mechanism exploration, and gene expression profiling—by delivering precision, depth, and adaptability to meet evolving scientific needs.