Molecular Diagnostics and Genetics

Precision Medicine for Personalized Care

Molecular Diagnostics and Genetics: Pioneering Precision in Healthcare

At MRB Next GenTech, we are at the forefront of advancing healthcare through the integration of molecular diagnostics and genetics. Our cutting-edge technologies and expert insights are transforming the landscape of medicine by enabling precise, personalized care that is tailored to the unique genetic profile of each individual.

Molecular diagnostic image

What We Do

Non-Invasive Prenatal Testing (NIPT)

NIPT uses a blood sample from the mother to determine the chance of a chromosomal condition in the developing baby from as early as the 10th week of pregnancy. 

Genetic Carrier Screening

Genetic carrier screening is a test that provides information for couples about the chance of having a child with any of the three most common inherited genetic disorders – cystic fibrosis, spinal muscular atrophy and fragile X syndrome.

Hereditary Cancer Testing

Genetic testing for identifying inherited cancer risks, providing personalized insights into prevention and early detection. Empowering individuals with the knowledge to make informed health decisions.

Pharmacogenomic Testing

Personalized medication management based on genetic makeup to optimize drug efficacy and reduce adverse effects. Tailored treatment plans for safer and more effective healthcare.

Cardiac Genetic Testing

Genetic analysis to assess inherited risks for heart conditions, enabling early intervention and personalized cardiac care. Protect your heart health with informed genetic insights.

Diagnostic Genetic Testing

Identify genetic causes of medical conditions through precise DNA analysis, aiding in accurate diagnosis and treatment planning. Uncover the genetic basis of your health concerns.

Oncology Genomic Testing

Comprehensive genomic analysis to guide cancer treatment decisions, targeting therapies based on tumor-specific genetic alterations. Enhance cancer care with precision medicine.

Infectious Disease Testing

Rapid and accurate detection of infectious pathogens through advanced genetic testing. Improve treatment outcomes with precise identification of infections.

Whole Exome Sequencing (WES)

Detailed analysis of the exome to uncover genetic variations linked to diseases and disorders. Provide comprehensive insights for precise diagnosis and personalized treatment.

Research & Development Support

Expert assistance in designing and executing innovative research projects, from concept to completion. Enhance your R&D efforts with tailored support and strategic guidance.

Our Commitment to Innovation

Our team of experts is dedicated to advancing the field of molecular diagnostics and genetics. Through our state-of-the-art facilities and commitment to scientific excellence, we are making significant strides in the fight against disease and the promotion of health on a global scale.

Meet Our Molecular Diagnostics Team

Our team of dedicated scientists and researchers is at the heart of MRB Next GenTech.org. With diverse expertise and a shared passion for biomedical innovation, we are committed to advancing health and science.

Frequently Asked Questions (FAQs)

Genetic testing involves analyzing your DNA to identify changes or mutations that could affect your health or the health of your children. These tests can provide valuable information for diagnosing conditions, guiding treatment, and informing family planning.
You can get tested by consulting with your healthcare provider, who will guide you through the process. Depending on the test, you may need to provide a blood, saliva, or tissue sample.
The time to receive results varies depending on the type of test. Some tests, like the Harmony® Prenatal Test, may return results within a week, while others, like Whole Exome Sequencing, may take several weeks.
Yes, your genetic test results are confidential and will only be shared with your healthcare provider and you. They will not be disclosed to third parties without your consent.