Genomics Centre

Your Trusted Partner in Genetic Testing for Health Insights

At our Genomic Medicine Centre, we are committed to advancing personalised healthcare through the power of genomics. Our team of experienced professionals is dedicated to providing personalised genomic medicine services that offer a deeper understanding of genetic factors influencing health, disease, and treatment outcomes.

With cutting-edge technologies and a compassionate, patient-centered approach, we empower individuals and families to make informed decisions about their health through comprehensive genetic testing and counselling.

Delivering Personalised Healthcare Through Genetic Testing

Genomic medicine is transforming the way we understand health, disease, and treatment. At our Genomic Medicine Centre, we believe in the power of genetics to guide medical decisions that enhance patient care and outcomes. Our services cater to individuals of all ages, from newborns to adults, and cover a wide range of genetic conditions.

Whether you’re seeking information about genetic testing, prenatal carrier screening, or counselling for genetic conditions, our expert team is here to help.

Genetic Testing Services We Offer

Clinical Genetic Services

Our clinical genetic services are designed to support patients who are experiencing unexplained medical conditions, birth defects, or a family history of genetic disorders. We provide comprehensive evaluations, including:

Genetic Testing and Diagnosis: Identifying genetic mutations or variations associated with specific conditions
Personalised Treatment Plans: Creating tailored healthcare strategies based on genetic findings
Support for Rare Diseases: Offering specialised counselling for patients with rare genetic disorders

Cancer Genetic Counselling and Testing

Understanding your genetic risk for cancer is crucial for early detection, prevention, and personalised treatment options. Our cancer genetic counselling services include:

Risk Assessment: Evaluating family history and personal medical history to determine cancer risk
Genetic Testing: Testing for hereditary cancer syndromes such as BRCA1, BRCA2, and Lynch syndrome
Post-Test Counselling: Helping individuals interpret their test results and navigate potential treatment or preventive measures
Preventive Measures: Providing recommendations for early screening, lifestyle changes, and medical interventions to reduce cancer risk

Family Planning Screening and Counseling

Genetic counselling before and during pregnancy can provide valuable insights into the health of both mother and baby. Our prenatal genetic counselling services include:

Carrier Screening for Couples: Identifying whether prospective parents carry genetic conditions that could affect their baby
Personalised Risk Assessment: Helping families understand the risks and making informed decisions about their pregnancy

Newborn Screening for Inborn Errors of Metabolism (IEM)

IEM is a genetic test that identifies inherited metabolic disorders that can lead to serious health problems if left untreated. Early detection allows for timely interventions to prevent irreversible damage, developmental delay, or even death. This test screens for a broad range of metabolic conditions using advanced analytical techniques

Why Choose Us for Genetic Testing?

Expert Team

Our team consists of experienced clinical geneticists, genetic counsellors, and multidisciplinary specialty consultants.

Patient-Centered Approach

We focus on individualised care and ensuring that patients and families are well-informed and supported throughout their genetic healthcare journey.

Cutting-Edge Technology

We collaborate with accredited local and international laboratories to ensure the quality of testing and interpretation of results.

Comprehensive Support

From diagnosis and counselling to treatment and long-term follow-up, we are here to guide you every step of the way.

Pre- and Post-Test Genetic Counselling

This will be provided by our experienced genetic counsellors.

Screenings We Offer

Reproductive Carrier Screening

This comprehensive genetic test is designed to identify whether an individual is a carrier of inherited genetic conditions. Carriers typically show no symptoms but can pass these conditions on to their children. This screening assesses the risk of passing on over 400 autosomal recessive and X-linked disorders, regardless of ethnic background.

Recommended For:

Individuals or couples planning to start a family
Women in early pregnancy (ideally their first trimester)
People with a family history of genetic disorders
Couples from high-risk ethnic backgrounds
Individuals undergoing IVF or other assisted reproductive technologies
Anyone who wants to better understand their genetic health risks before conception

Conditions This Test Screens For :
This test covers 400+ autosomal recessive and X-linked genetic conditions, including:

Blood disease – Alpha thalassemia, beta thalassemia, and sickle-cell disease
Metabolic disease – G6PD
Nervous system – Spinal muscular atrophy
Development – Fragile X syndrome
Musculoskeletal system – Duchenne muscular dystrophy

Newborn Screening for Inborn Errors of Metabolism (IEM)

This genetic test identifies inherited metabolic disorders that can lead to serious health problems if left untreated. Early detection allows for timely interventions to prevent irreversible damage, developmental delay, or even death. This test screens for a broad range of metabolic conditions using advanced analytical techniques.

Recommended For:

All newborns (ideally within 48–72 hours after birth)
Infants with unexplained symptoms such as poor feeding, vomiting, seizures, or developmental delay
Families with a history of metabolic disorders
High-risk pregnancies (e.g., consanguineous marriages or abnormal prenatal findings)
Siblings of children diagnosed with IEM

Conditions This Test Screens For:
This test covers 30++ metabolic conditions across multiple categories, including:

Amino acid disorders – e.g., phenylketonuria (PKU), maple syrup urine disease (MSUD)
Organic acidemias – e.g., Methylmalonic acidemia (MMA), propionic acidemia
Fatty acid oxidation disorders – e.g., MCAD deficiency, LCHAD deficiency
Urea cycle disorders

Cancer Genetic Risk Panel

This genetic test identifies inherited mutations associated with an increased risk of various cancers. Early detection of these mutations enables individuals and healthcare providers to take proactive steps in surveillance, prevention, and treatment strategies. This panel analyses multiple genes known to significantly increase the risk for hereditary cancer syndromes.

Recommended For:

Individuals with a personal or family history of cancer (especially early-onset or multiple cancers)
People with relatives who have known hereditary cancer syndromes (e.g., BRCA mutations)
Individuals interested in understanding their genetic predisposition to cancer

Conditions This Test Screens For:
Including: