Aurora™ Non-invasive Prenatal Testing (NIPT)

Aurora™ is a non-invasive prenatal test (NIPT). By collecting 6-10 mL of the mother's blood, extracting cell-free DNA and using low-depth whole-genome sequencing technology, then combining bioinformatic analysis, the chance of fetal chromosomal abnormalities can be determined.

Aurora™ is a safe and accurate method for detecting trisomies 21, 18 and 13. It can also be expanded to detect other autosomal or sex chromosome aneuploidies and the most prevalent micro-deletions/duplications (CNVs).

Aurora™ Extended checks for 90+ rare conditions, including:

  • DiGeorge syndrome (a leading cause of heart defects and learning difficulties)

  • Wolf-Hirschhorn, Cri-du-Chat, Prader-Willi/Angelman and more

Here is the sample request and collection procedure.

Genetic counselling will be offered free-of-charge to all whose test result indicates a pregnancy with high probability of chromosomal abnormality.

Affinity™ Reproductive Carrier Screening (RCS)

Affinity™ is a reproductive carrier screening test (RCS). It helps parents to understand their chances of passing on serious genetic conditions to their children by detecting genetic risks and providing reproductive guidance.

Affinity™ covers more than 170 recessive and X-linked monogenic conditions, including CF, SMA, Fragile X, DMD and thalassaemia. It assesses for more than 10,000 known disease causing variants in 165 genes.

Affinity™ testing can be carried out either before or during pregnancy (before the 16th week). If a patient is already pregnant, the patient’s reproductive partner should be tested concurrently to ensure accurate estimation of risk and timely management.

Here is the sample request and collection procedure.

Genetic counselling will be offered free-of-charge to couples identified as being at high-risk of having a child affected with an inherited disorder that can cause serious illness.

AbsoluteBiome™ Microbiome Testing

AbsoluteBiome™ is a faecal microbiome test for clinicians and researchers. Measuring actual microbial levels, it provides clear, evidence-based insights to support clinical care and research.

The human microbiome is a dynamic and highly complex ecosystem containing trillions of bacteria, viruses and fungi, uniquely adapted to each individual. Disruptions in the balance of the microbiome have been linked to a wide range of health conditions, including gastro-intestinal disease, metabolic disorders, immune dysfunction and some neurological conditions.

Whole Genome Sequencing (WGS)

We offer WGS services utilising DNBSEQ™ technology. Multiple instrument options are available to accommodate different project scales and requirements. We support a wide range of sample types including: ​​

  • Whole blood ​

  • Saliva and buccal swabs​

  • Fresh frozen tissue​

  • Cell pellets​

  • Microbial isolates​

  • Extracted DNA​

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