DNA NGS sequencer Uniseq 2000

for RNAfor researchlaboratory

PRODUCTION INTRUDUCTION UniSeq2000TM is a monochrome fluorescence-based，highly compact and automatic gene sequencer designed for clinical applications. With the design of monochrome fluorescence, it dramatically simplifies the optical systems and sequencing reagent cost. Furthermore, it compatible with the library structures of mainstream sequencing platform. KEY APPLICATION 1、Low-depth Whole Genome Sequencing (e.g. Copy number variation detection, Preimplantation genetic screening, noninvasive prenatal testing, etc.) 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. microbial metagenomics, isolated bacteria, etc. ) Demo Data in Different Applications Copy number variation detection Uniseq2000TM is used for copy number variation detection in one clinical medical research center to screening the fetal chromosomal abnormal. Uniseq2000 can effectively identify Chr18 trisomy, Chr14 trisomy and part chromosomal chimerism. This allows the laboratory to detect microduplication and microdeletion from 30Mb to 2Mb.