Next Generation Genetic Testing

Our next generation sequencing genetic panels offer a wide range of applications and are compatible with leading sequencing technologies, providing highly accurate and comprehensive genomic analysis for testing laboratories and healthcare institutions.

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• Easy library preparation: Simplifies the complex NGS library preparation process with straightforward molecular biology techniques.

• Comprehensive coverage: Detects a variety of mutation types, including single nucleotide variants (SNVs), multi-nucleotide variants (MNVs), insertions, deletions, indels, and copy number variations (CNVs).

• High sensitivity: Capable of detecting low-frequency genetic mutations, suitable for low-abundance sample analysis.