Novo Genomics

Unlock your
Wellness Potential

WellDNA unlocks the secrets of your DNA, offering a personalized approach to wellness by analyzing your genetic predispositions in key areas such as health, nutrition, fitness, and medication response. This comprehensive genetic report serves as your lifelong guide to optimizing well-being, enabling you to make proactive and informed lifestyle choices.

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Not for diagnostic use

Novo Biome

Gut Microbiome Test

Guts insight for a
healthier you

Gut Microbiome testing has proved as a powerful tool for understanding and improving the human health. At Novo Genomics, this screening method will analyze the complex group of microorganisms residing in the digestive tract. This can help to improve the quality of the health of the individual.

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Not for diagnostic use

Novo-NIPT®

Safe, Simple, Early Insights for
Your Baby's Health

Non-Invasive Prenatal Testing

Novo-NIPT is a simple and safe blood test that checks for the risk of genetic conditions, like Down syndrome, in a baby as early as 10 weeks of your pregnancy.

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SAFE

ACCURATE

SIMPLE

FAST

Pharmacogenomics

Test Once, Optimize Forever
– Smarter Meds, Fewer Side Effects.

Pharmacogenomics is the study of how an individual's genetic makeup affects their response to medications. By analyzing genetic variations that influence drug metabolism, efficacy, and potential side effects, pharmacogenomics enables personalized treatment plans tailored to the patient's unique genetic profile.

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PRS for Breast Cancer

Predict. Prevent. Protect.
– Your DNA Knows What’s Coming.

Polygenic Risk Score (PRS) for breast cancer is a genetic test that helps predict the likelihood of someone developing breast cancer based on their genes.

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PRS for Coronary Heart Disease

Know Your Heart’s Future
– Today.

Polygenic Risk Score (PRS) for coronary artery disease is a genetic test that helps predict your risk of heart disease by analyzing thousands of small genetic changes in your DNA.

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SMN1 & SMN2 Genetic Testing

Know Before Symptoms Start
– Early SMA Testing Saves Futures.

A genetic test that analyzes the SMN1 and SMN2 genes to diagnose Spinal Muscular Atrophy (SMA), a condition that causes muscle weakness and can lead to infant mortality.

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Whole Exome Sequencing (WES)

Unlocking the Genetic Code
– for Better Health and Care

Whole Exome Sequencing is a diagnostic test that analyzes the protein-coding regions of your DNA. It helps identify genetic changes linked to diseases and health conditions.

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Carrier Screening Sequencing

Know Your Genetic Risk,
Protect Your Future.

Carrier Screening Sequencing is a test that helps identify whether you carry a gene for certain inherited conditions, even if you don’t have symptoms.

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Whole Genome Sequencing

A Complete Genetic Profile
for Health Insights

Whole Genome Sequencing (WGS) is a comprehensive test that analyzes nearly all of your DNA. It provides a complete picture of your genetic makeup to identify genetic variations that can impact your health.

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Marital Genetic Testing

Plan Your Future Together with Confidence
– Understand Your Genetic Risks Before Marriage

Marital Screening is a genetic test designed to identify inherited conditions that could affect you and your partner, ensuring a healthy future for both individuals and any potential children.

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BRCA1 & BRCA2 Screening

Take Control of Your Health
– Detect BRCA1 & BRCA2 Early, Protect Your Future

BRCA1 & BRCA2 Screening is a genetic test designed to identify mutations in the BRCA1 and BRCA2 genes (Breast Cancer 1 and 2 genes), which significantly increase the risk of developing breast, ovarian, and other cancers.

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What we offer?

Product and Clinical Services

Pharmacogenomics

This test helps prevent bad reactions to medications and ensures you get the best treatment for your unique genetic makeup.

Polygenic Risk Score (PRS)

PRS helps detect heart disease risk early, even before symptoms appear, so you can take action to protect your heart health.

Genetic Counseling

Provides a personalized risk assessment, going beyond family history to include genetic factors.

SMN1 & SMN2 Genetic Testing for Spinal Muscular Atrophy (SMA)

Early diagnosis of SMA is critical for initiating effective treatments that can improve quality of life and reduce disease progression.

Non-Invasive Prenatal Testing (NIPT)

NIPT helps expectant parents get early insights about their baby’s health without the risks of invasive procedures.

Whole Exome Sequencing (WES)

WES helps doctors and scientists identify genetic disorders quickly and accurately, leading to better treatment and care.

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Why Us?

Preventive

Proactive paradigm where diseases can be anticipated and prevented, ensuring healthier lives and improved outcomes.

Diagnostic

Provide definitive answers by confirming or ruling out a diagnosis, enabling clarity and guiding effective medical care.

Treatment

Empowering physicians enabling them to choose the most effective medication and treatment at the optimal dose.

Accreditations and Certifications

Novo Genomics is accredited by CAP (College of American Pathologists), CBAHI (Saudi Central Board for Accreditation of Healthcare Institution) and certified by the Ministry of Health, ensuring the reliability and high standards of our testing services.

Innovative Partnerships

Our collaborations with reputable companies like Oxford Nanopore Technologies and Lenovo demonstrate our commitment to cutting-edge genomics technology and innovation.

Diverse Applications

We offer genetic testing not only for humans but also for animals and plants, showcasing the wide-ranging expertise in multi-omics technologies.

Patient-Centered Approach

Novo Genomics emphasizes care, innovation, and integrity in their services, aiming to empower patients with personalized health insights and solutions.

Saudi Market Leader

As a prominent genomics company in Saudi Arabia, Novo Genomics contributes to advancing healthcare through its specialized services in the region.

Focus on Preventive Healthcare

Our diagnostic and preventive genetic testing services support personalized medicine, which can lead to better health outcomes and more targeted treatments.