Making Omics Work in Everyday Medicine

Scalable, diagnostic-grade programs designed to integrate with your clinical workflow.

We provide NGS-based diagnostic programs and whole-genome sequencing with virtual panels, designed to support early diagnosis, personalised treatment, and ongoing clinical care. As the official testing laboratory of the Emirati Genome Program, our solutions are validated at population scale, deployed in active clinical practice, and delivered in partnership with pharmaceutical companies.

Delivered by a multidisciplinary team of clinical geneticists, genetic counsellors, variant scientists, and pathologists, operating from a CAP-accredited, ISO 15189 certified laboratory

Clinical Focus Areas

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Cardiology

Validated workflows and deep coverage ensure high sensitivity and specificity, supporting reliable results for diagnostics, screening, and genomic reporting.

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Endocrinology

Validated workflows and deep coverage ensure high sensitivity and specificity, supporting reliable results for diagnostics, screening, and genomic reporting.

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Reproductive
Health

Optimized protocols and automation deliver results with minimal delay—ideal for time-sensitive applications such as newborn screening and urgent clinical cases

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Pediatric &
Rare Disorders

From targeted gene panels to whole genomes, our flexible sequencing infrastructure adapts to a wide range of project sizes and scientific goals.

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Oncology (Germline, Somatic & Liquid Biopsy)

Validated workflows and deep coverage ensure high sensitivity and specificity, supporting reliable results for diagnostics, screening, and genomic reporting.

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Neurology & Neurodevelopmental Disorders

Integrating genomics across every stage of life to inform prevention, early diagnosis, and treatment.

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Ophthalmology

Management of brain, spine, and nervous system disorders with advanced diagnostics and neuro-rehabilitation.

Core Offering

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Liquid Biopsy for Cancer

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Screening

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Minimal Residual Disease (MRD) Testing

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NIPT (Non-Invasive Prenatal Testing)

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Premarital & Pre-IVF Screening

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Newborn Screening

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Pharmacogenomics

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Whole Genome-Based Diagnostics with Virtual Panels

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Somatic Tumour Profiling

Access our complete range of

NGS-based diagnostic tests, clinical reports, and service information.

  • "Biogenix's omics-powered programs are changing how we approach cancer care — giving us the biological precision to make better treatment decisions every day."

    Dr. Stephen Grobmyer

    Chief, Cancer Institute
    Cleveland Clinic Abu Dhabi

  • "For paediatric and neuro-ophthalmic conditions, early and precise diagnosis changes everything. Biogenix gives us the genomic tools to get there faster."

    Dr. Arif Khan

    Section Head, Paediatric & Neuro-Ophthalmology
    Cleveland Clinic Abu Dhabi

  • "Genomics is transforming how we understand and manage inherited metabolic disorders. Biogenix has been central to advancing that work in the UAE."

    Dr. Fatima Al Jasmi

    Chair, Department of Genetics & Genomics
    UAE University | Metabolic Consultant, Tawam Hospital

  • "Pharmacogenomics is no longer a future concept — it is clinical practice. Biogenix has made that a reality for our patients."

    Dr. Sara Suliman

    Consultant, Endocrinology & Diabetology
    Imperial College Diabetes Centre

  • "From premarital screening to prenatal testing, Biogenix supports every stage of the reproductive health journey with the precision our patients deserve."

    Dr. Summia Zaher

    Dr. Summia Zaher
    CEO & Consultant, Obstetrics & Gynaecology

Download related cutting-edge research -
White Papers & Though Leadership

How we can help deliver precision,
prediction, and prevention at scale?