We are committed to remaining on the cutting edge of genomics and molecular diagnostics. We improve our testing capabilities for the benefit of the researchers, clinicians and patients who rely on us for accurate and reliable molecular data.
Clinical molecular genetic services
Our services help clinicians determine the molecular causes of human diseases. We provide actionable molecular information that clinicians can exploit to prevent, diagnose or monitor diseases, make informed decision and guide therapies. The goal is to to provide the most efficient care for each patient.
Diagnostic and carrier testing for inherited genetic disorders
Predictive and pre-symptomatic complex testing for adult-onset and disorders
Pharmacogenetic testing to help with drug selection, dosage and response for patients
Prenatal and postnatal testing for chromosomal Abnormalities
Genomic Services
We help identify unique genomic influences that account for differential disease manifestations between and across populations. Variations specific to populations and individuals may facilitate tailored therapies and minimize adverse drug effects.
Please contact us for discussion on how we can help
Some of Our Expertise
Molecular Genetics
Genomic Medicine
Pharmacogenetics
Research and Training
Clinical Trials
Next generation Sequencing
Genotyping
Infectious disease
DNA banking
Biomedical Data Analytics
We can leverage different state-of-the-art molecular diagnostic platforms and technologies to develop and customize assays. We also have the ability and flexibility to offer custom services and solutions that suit the need of each customer.