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Clinical Genomics, Simplified.

Your partner for setting up, developing, and delivering high-quality sequencing testing services to your community with our NGS and LRS solutions

Send-out Testing

Send samples directly to our accredited labs​

End-to-End Turnkey Solution

We supply the lab tech transfer solution (such as reagents, SOPs, LIMS software, and training) to build your own sequencing capabilities 

Custom Panel

Leverage our R&D team, labs, and production plant to co-develop custom panels tailored to your specific research or clinical targets

Our Solutions

Flexible Models for Every Partner

Whether you need a reliable reference lab or want to build your own sequencing facility, we have the infrastructure to support you

From the proven reliability of NGS to the cutting-edge precision of LRS, we match the technology to your needs

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Next-Generation Sequencing (NGS)

For Broad Clinical Applications

Panel

Expanded Carrier Screening

Screening for hundreds of inherited conditions to support reproductive planning​

Newborn Genetic Screening

Designed to complement and expand the scope of biochemical newborn screening

Prenatal Screening

NIPT

Non-invasive screening for fetal chromosomal abnormalities (e.g. trisomy 21)

NIPT-SGD

Non-invasive screening for fetal AD/XL single-gene disorders mainly caused by de novo mutation

Rare Disease & Prenatal Diagnosis

WES / Prenatal WES

Phenotype-driven analysis (+ genotype-driven analysis for prenatal WES) for complex genetic conditions

CNV-seq

Designed for first-tier prenatal diagnostics, miscarriage analysis and molecular diagnosis

Long-Read Sequencing (LRS)

Deeper Insight into Conditions That May Be Difficult to Resolve Using NGS and Other Molecular Assays

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