Fortis Institute of Genomic Medicine

About the Fortis Institute of Genomic Medicine

Fortis Center for Excellence in Genomics

The Fortis Center for Excellence in Genomics (CEG) is India’s leading hub for precision diagnostics, innovation, and research in the field of genomics. Located at Fortis Memorial Research Institute, Gurugram, the CEG integrates ultrafast molecular diagnostics, AI-powered bioinformatics, and a multidisciplinary team to offer personalized solutions for both benign and malignant disorders.

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  • Why Genomics?

    Genomics is the study of your entire DNA – not just one or two genes. It helps us:

    • Detect inherited conditions early
    • Classify complex diseases like cancer more accurately
    • Guide targeted therapies
    • Predict treatment response and monitor residual disease
    • Personalize care like never before

  • What We Offer

    1. Benign Genomics
      1. Inherited cancer risk (e.g. BRCA1/2, Lynch syndrome)
      2. Thalassemia, sickle cell disease carrier screening
      3. Neurogenetics (epilepsy, ataxia, muscular dystrophy)
      4. Pediatric disorders (developmental delay, autism, syndromes)
      5. Cardiogenetics (arrhythmias, cardiomyopathies)
      6. Pharmacogenomics (drug metabolism and adverse reaction prediction)
      7. Nutrigenomics & Wellness
    2. Malignant Genomics
      1. Solid Tumors: Breast, lung, colon, prostate, ovary, etc.
      2. Hematologic Malignancies: Leukemia, lymphoma, myeloma
      3. Liquid Biopsy & ctDNA for real-time cancer tracking
      4. CAR-T and transplant eligibility panels
      5. Minimal Residual Disease (MRD) by NGS
      6. CHIP and pre-leukemic state detection
      7. Fusion gene detection and novel mutation analysis

  • Unique USPs of Fortis Genomics

    • India’s first real-time NGS platform (Ion Torrent Genexus) for same-day reports
    • Multispecialty Genomic Tumor Boards
    • AI Club-powered precision bioinformatics
    • Home-grown expert team of molecular oncologists, geneticists, and bioinformaticians
    • Integrated reporting aligned with global guidelines (AMP, CAP, ASCO, ACMG)
    • Multi-language patient-centric reports for better understanding
    • Genomic counseling for patients and families
    • National registries and research leadership (e.g., AML, CHIP, CAR-T, lymphoma)
       

  • Research and Innovation

    Fortis is proud to lead several national and institutional research initiatives:

    • India’s largest AML Genomic Study
    • ctDNA monitoring for DLBCL
    • AI-based prediction models in transplant and cancer genomics
    • Launch partner for India’s first Genomic Registry on CHIP and pre-malignant clones
       

Our Hospitals

Our Speciality

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    Medical Genetics

FAQs

  • 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.
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