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1. Targeted enrichment of pathogenic sequences through specific amplification, eliminating the need to remove human genomic DNA, unaffected by host nucleic acids.
2. PCR + NGS dual-platform approach amplifies signals for deep sequencing, combining sensitivity and specificity.
3. Simultaneous construction of libraries for DNA and RNA targets, simplifying operations while saving costs and time.
4. Designing different numbers of targets based on the pathogenicity levels and sequence features of pathogens, reducing the risk of missed detections.
5. Typing and identification of special pathogens with rich genomic diversity, capable of covering multiple subtypes.
6. Simultaneous capture of "pathogen + drug resistance + virulence" with optimized ratios, assisting in precise treatment while rationally distributing data volume.
7. Dual barcode sequencing, offering a rich combination to avoid barcode duplication and reduce the impact of laboratory aerosols on results.
8. Inclusion of error-proof labels and internal controls for quality control throughout the entire process.
9. Customizable, upgradeable, and optimized panels, supporting the timely addition of newly emerging pathogens.
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BBS