NGS Library Preparation Kits
Our next-generation sequencing kits streamline library construction across various platforms, enabling:
- Whole genome and exome sequencing
- Targeted resequencing panels for cancer, rare diseases, and pharmacogenomics
- Amplicon- and hybrid-capture-based methods optimized for low-input samples
- Microbiome, metagenomics, and transcriptomics applications across research and clinical fields
Designed with enzyme fidelity, barcoding flexibility, and automation-friendly workflows, these kits reduce variability and enhance sequencing success rates.
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