Fortis Institute of Genomic Medicine
About the Fortis Institute of Genomic Medicine
Fortis Institute of Genomic Medicine is India’s leading hub for precision diagnostics, innovation, and research in the field of genomics. Located at Fortis Memorial Research Institute, Gurugram, integrates ultrafast molecular diagnostics, AI-powered bioinformatics, and a multidisciplinary team to offer personalized solutions for both benign and malignant disorders.
Where Precision Meets Personalized Cancer Care
At the Fortis Institute of Genomic Medicine, we are revolutionizing the approach to cancer diagnosis, treatment, and management by harnessing the full potential of genomic science. As a leading Centre of Excellence, our institute is dedicated to providing state-of-the-art, individualized care that leverages the latest advancements in genomic technology and research.
Pioneering the Future of Cancer Care
Cancer is not a single disease but a group of diseases, each unique in its molecular and genetic makeup. At Fortis, we recognize that every cancer diagnosis is different, and thus, every treatment approach should be tailored to the individual. Our genomic medicine program allows us to go beyond traditional methods by analyzing the genetic alterations and mutations that drive cancer growth. By decoding the molecular structure of tumors, we gain crucial insights that guide personalized treatment strategies, ensuring that patients receive the most effective therapies with fewer side effects.
Our approach is rooted in precision medicine, which focuses on targeting the underlying genetic factors of cancer rather than just treating symptoms. This allows us to offer more effective and customized care, empowering patients with the knowledge and treatment options that are best suited to their unique condition.
Our Hospitals
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Fortis Hospital, Mohali
4.6
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Fortis Memorial Research Institute, Gurgaon4.6
FAQs
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Is genomic testing only for cancer patients?
No. Genomic testing is useful in a wide range of conditions, from inherited disorders and pediatric syndromes to lifestyle-based wellness optimization. -
How is genomics different from a routine blood test?
Routine blood tests show what’s happening now. Genomics shows what could happen, how your body might respond to treatments, and what risks you may carry. -
Can I do genomic testing without a doctor’s prescription?
While many tests are available directly, we recommend a specialist consultation to choose the right test and interpret results appropriately. -
Is genomics safe? Will it affect my insurance or job?
Genomic testing is safe and only involves a blood or saliva sample. In India, genetic discrimination laws are evolving, and your results are handled with the utmost confidentiality. -
What is CHIP?
Clonal Hematopoiesis of Indeterminate Potential (CHIP) is a pre-leukemic condition where healthy individuals have mutations in blood-forming cells. Early detection can help monitor cancer risk. -
Fun Genomics Facts
• Your DNA could stretch from Earth to the moon and back — over 100,000 times.
• 99.9% of your DNA is identical to every other human. It’s the 0.1% that makes you… you.
• You have more bacterial DNA in your body than human DNA.
• Genomics helped identify the exact COVID-19 strain in days — a process that took years before. -
Why Is Genomics Important?
Genomics is transforming the landscape of modern healthcare by providing deeper insights into the genetic underpinnings of disease. It plays a crucial role in everyday primary care, offering valuable information for diagnosing, managing, and even preventing a wide range of health conditions.
One key area where genomics has a significant impact is in the diagnosis of rare diseases. Although each rare disease may affect only a small number of individuals, collectively they impact around 1 in 17 people—making them surprisingly common in clinical practice. Genomic testing can help identify these conditions early, often after years of inconclusive symptoms, enabling targeted treatments and improved patient outcomes.
Genomics is also pivotal in understanding and managing chronic and complex diseases like cancer, diabetes, cardiovascular disease, and certain autoimmune disorders. By uncovering the genetic variations that contribute to these conditions, clinicians can offer more personalized treatment plans—often referred to as precision medicine—which can be more effective and carry fewer side effects.
In essence, genomics is no longer a niche area of science—it is becoming a fundamental part of proactive, personalized, and preventive healthcare.