Dna Ngs Sequencer

INTRODUCTION TO PRODUCTION

UniSeq2000TM is a monochrome fluorescence-based gene sequencer that is highly compact and automatic, specifically designed for clinical applications. The optical systems and sequencing reagent cost are significantly simplified by the monochrome fluorescence design. Additionally, it is compatible with the library structures of the most common sequencing platforms.KEY APPLICATION

1. Whole genome sequencing with low depth

(e.g., noninvasive prenatal testing, preimplantation genetic screening, and copy number variation detection)

2. Targeted Sequencing (Hybridization capture/multiplex PCR-based)

(e.g., inherited diseases panel, microbial and drug resistance genes panel, oncology panels, etc.)

3. Small Whole Genome Sequencing(e.g., isolated bacteria, microbial metagenomics, etc.)Demonstration Data in Various ApplicationsDetection of copy number variationsIn a single clinical medical research center, Uniseq2000TM is employed to detect copy number variations and screen for fetal chromosomal abnormalities. Chr18 trisomy, Chr14 trisomy, and part chromosomal chimerism can be accurately identified by Uniseq2000. This enables the laboratory to identify microduplication and microdeletion in the range of 30Mb to 2Mb.