Comprehensive reproductive genetic sequencing screening identifies genetic risks in advance. With precise, science-based testing, it supports safe pregnancies and safeguards the health of new lives.
Tumor genetic sequencing supports cancer risk assessment, targeted therapy matching and postoperative recurrence monitoring. Accurate genomic analysis enables personalized full-cycle anti-tumor care to protect patient health.
Whole Exome Sequencing (WES) enables accurate analysis of human exons. It is widely applied in rare disorder identification, hereditary cancer screening and prenatal genetic diagnosis.
HLA typing accurately identifies human leukocyte antigen genotypes, supporting organ transplant matching, recurrent miscarriage investigation and autoimmune disease risk evaluation.
tNGS enables accurate identification of targeted pathogens with high efficiency and cost-effectiveness.
eDNA from the environment enables detection of resident species' taxonomic and functional traits for ecological research.
Single-cell sequencing enables generation of high-quality single-cell and spatial omics data to study cell heterogeneity, tumor microenvironments and development.
Two-color / four-color optics with ultra-high sensitivity for fluorescence signal capture
High stability and reliability, with effective resistance to ambient temperature fluctuations and vibration interference
Unique terminator nucleotide structure, highly efficient SBS (Sequencing by Synthesis) reaction
Research and production capabilities of high-fidelity polymerase mutants
High-density, low-noise surface chemical modification
Flow cell design compatible with mainstream NGS libraries
Raw data processed via AI & machine learning for basecalling
Application-oriented databases and bioinformatics software
