Genetic & Molecular Testing

Decoding Cancer at the Molecular Level

Genetic & Molecular Testing has transformed the way cancer is diagnosed and treated by providing deeper insights into the biological and genetic characteristics of a tumour. Rather than relying solely on conventional diagnostic methods, these advanced tests identify specific genetic alterations, molecular markers, and protein expressions that influence how a cancer develops and responds to treatment. At Apulki Medical Centre, comprehensive in-house molecular diagnostics, including Next Generation Sequencing (NGS), Fluorescence In Situ Hybridisation (FISH), Immunohistochemistry (IHC), and genetic testing, play a vital role in enabling personalised and precision-driven cancer care.

Advanced Molecular Diagnostics for Precision Oncology

All Your Diagnostics, Under One Roof

At Apulki Medical Centre, all molecular diagnostic services are available under one roof, ensuring greater convenience, faster turnaround times, and seamless coordination between the laboratory and the clinical team. Performing these specialised investigations in-house allows our oncologists, pathologists, and molecular scientists to work closely together, enabling timely diagnosis and quicker treatment planning without unnecessary delays. This integrated approach supports informed clinical decision-making and ensures that patients receive the right treatment at the right time.

All Your Diagnostics, Under One Roof

At Apulki Medical Centre, all molecular diagnostic services are available under one roof, ensuring greater convenience, faster turnaround times, and seamless coordination between the laboratory and the clinical team. Performing these specialised investigations in-house allows our oncologists, pathologists, and molecular scientists to work closely together, enabling timely diagnosis and quicker treatment planning without unnecessary delays. This integrated approach supports informed clinical decision-making and ensures that patients receive the right treatment at the right time.

The Technology Behind Precision Diagnosis

Our advanced diagnostic capabilities include Next Generation Sequencing (NGS), which analyses multiple genes simultaneously to identify mutations associated with different cancers and guide precision therapies. Fluorescence In Situ Hybridisation (FISH) detects specific genetic abnormalities that are important for diagnosing certain cancers and selecting appropriate treatments. Immunohistochemistry (IHC) evaluates protein expression within tumour cells, helping classify cancers and predict their response to therapy. In addition, genetic testing can identify inherited genetic changes that may increase an individual’s risk of developing certain cancers, enabling risk assessment, family counselling, and preventive care where appropriate.

Genetic and molecular testing is valuable across a wide range of cancers, including breast, lung, colorectal, ovarian, prostate, gastrointestinal, and blood cancers, among others. The results help clinicians determine whether targeted therapies, immunotherapies, or other precision treatments are likely to be beneficial, reducing unnecessary treatments and supporting a more personalised approach to cancer care. These tests also contribute to monitoring disease progression, evaluating treatment response, and identifying changes that may influence future treatment decisions.

At Apulki Medical Centre, Genetic & Molecular Testing forms an integral part of our precision oncology programme. By combining advanced laboratory technology, specialised expertise, and multidisciplinary collaboration, we provide accurate molecular insights that support timely diagnosis, personalised treatment planning, and evidence-based cancer care. Our commitment to in-house diagnostics ensures that patients benefit from comprehensive, coordinated, and precision-driven care throughout every stage of their treatment journey.