Synchronous Detection of Methylation and Mutation No need for conversion to preserve the original sequence
One sample, one hybrid reaction, one set of probes Learn More
for 9 major cancer types in a single detection Learn More
tNGS pathogen detection solution Learn More
Best Solution for MRD Ultra-Stable for several Kb-level Panel
Same day from sample to capture-based library
High-Sensitive for extremely low frequency variants Learn More
Online Design Platform Optimization design algorithm based on > 1 million probes
Complete the design and evaluation within 10 minutes
NGS QC based quality inspection delivery Learn More
Providing NGS total solution on MGI/Illumina platforms,
including library preparation and hybridization capture. Learn More
Our Products
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NadPrep LibraryNGS library preparation
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μCaler (Ultra-sensitive Probes)Stable hybridization capture for mini-panels with ultra-sensitive within a single day
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NadHybLibrary preparation & Targeted capture
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NadPanel (Conventional Probes)Inventoried panels for hybridization capture
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NadProbeA one-stop service covering the entire process from probe design, probe production, quality inspection, optimization, and result delivery.
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NadInstrumentNadAuto-series Fully-automated NGS Workstations
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Universal Stubby Adapter (UDI)
Sequencing single library on Illumina and MGI platform.
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Minimum balanced group only requires 4 libraries. -
Low-frequency Mutation Analysis
By tagging both ends of the double-stranded DNA molecule and incorporating
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with the error correction algorithm, molecular identifiers enable reduced error
rate and higher accuracy in low-frequency mutation analysis.
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