
Saudi-Based Leader in Genomics Innovation
Rooted in national pride, Novo Genomics is Saudi Arabia’s pioneering genomics laboratory, driving innovation in healthcare and supporting the Kingdom’s Vision 2030.
Passion & Integrity
Relentless Passion for Science Unwavering Integrity and Trust
Client-Centered Excellence
Deep-rooted Client Commitment Data Accessibility & Transparency
Innovation with Purpose
Continuous Innovation & Excellence Purposeful Social Responsibility

Non-Invasive Prenatal Testing (NIPT)
A simple and safe blood test that checks for the risk of genetic conditions, like Down syndrome, in a baby as early as Basic -10 weeks into pregnancy & Plus 12 weeks.
Passion & Integrity
Relentless Passion for Science Unwavering Integrity and Trust
Client-Centered Excellence
Deep-rooted Client Commitment Data Accessibility & Transparency
Innovation with Purpose
Continuous Innovation & Excellence Purposeful Social Responsibility

Research and
Development
We support academic researchers with advanced NGS services across industries—from pharma to agriculture so they can focus on impactful results and breakthroughs in personalized medicine.
Passion & Integrity
Relentless Passion for Science Unwavering Integrity and Trust
Client-Centered Excellence
Deep-rooted Client Commitment Data Accessibility & Transparency
Innovation with Purpose
Continuous Innovation & Excellence Purposeful Social Responsibility
What We Offer & Why Choose Us
Experience the difference — cutting-edge services designed to elevate care and deliver results.
Genetic Testing
Identifies inherited health conditions to enable early intervention and preventive care.
Oncology Diagnostics
Provides molecular profiling to match cancer patients with the most effective, personalized treatment options, improving clinical outcome.
Pharmacogenomics
Analyzes genetic markers to prevent adverse drug reactions and optimize therapy selection based on each patient’s unique genetic makeup.
Prenatal Screening
Offers non-invasive early-pregnancy tests to assess fetal health and detect potential genetic disorders.
Rare Disease Diagnosis
Utilizes a proprietary polygenic risk score, developed specifically for the Saudi population, to enhance diagnostic accuracy and enable targeted treatment strategies.
Clinical Research Support
Supplies genomic data, analytics, and related services to accelerate clinical and academic research, with plans to expand offerings to pharmaceutical companies.
Client Testimonials
What our clients say about our services
"Praise be to God, they had a NIPT test, frankly, with professional treatment and respect for appointments, and the result also came out within five days, including Weekend."

malak alhashmy
"I had a NIPT test done by Novo Genomics, and I can say that it is the best laboratory I have tried in Riyadh. I have tried many laboratories to do different tests, but this laboratory is distinguished by: 1- Good reception, dealing, and responding to your inquiries via WhatsApp at all times. 2- Excellent service quality consistent with the price 👍 3- A detailed report of the fetus. After several recommendations and laboratory visits, I confidently recommend Novo Genomics ✨"

Maram Albluwi
"A unique laboratory conducted a genetic analysis and based on what they told me, it was a complex analysis that required time and scrutiny, but the results appeared ahead of time and the results were explained well. I learned that they also have genetic pregnancy testing which impressed me with how advanced they are. I strongly advise everyone who wants to avoid any type of genetic disease to visit this laboratory for early detection. I thank the group for their elegant treatment."

Zakiah A
"Frankly speaking, the experience was the first time I dealt with them. They were very quick to respond. They made an appointment for me at home on their appointment, and there was no delay. The result was not delayed exactly as they said, 7 days. God willing, I wish them success, Lord."

Wejdan Sunbol
"I had a NIPT basic test last week and the results came out in less than a week. Their treatment in the laboratory was very elegant and the staff were professional. They were all cooperative and ready to answer all questions. "

saba altalhi
"I had a genetic test done by them, one of the best, finest, and cleanest clinics. They were very cooperative with many questions I asked, but they were answering and appreciative. May God make them happy. The results came out before the due date. Thank you for all this kindness 🤍🤍🤍 "

دعاء الغامدي
"Thank you for the good treatment and quick response. My test results came out in less than a week💜💜"

nada alsudais
"Professional and sophisticated treatment. To be honest, it was an excellent experience 👍 … "

Sarah 630
"Best and safest place to test your sample"

AbdulMajeed Samhouri
Genetic Testing

Scientific Description
Analyzes an individual's DNA to identify inherited health conditions. Whole Genome Sequencing (WGS) examines the entire genome, detecting rare variants and structural changes, while Whole Exome Sequencing (WES) focuses on protein-coding regions (~1.5% of the genome), where ~85% of disease-causing mutations occur. Targeted Gene Panels provide a cost-effective, high-yield approach for specific conditions (e.g., cardiovascular or metabolic disorders), enabling early intervention and personalized prevention.
Specific Tests
- Whole Genome Sequencing (WGS)
- Whole Exome Sequencing (WES)
- Targeted Gene Panels
Oncology Diagnostics

Scientific Description
Leverages molecular profiling to identify genetic and epigenetic alterations in cancer. Cancer Panels detect hereditary (e.g., BRCA1/2) and somatic mutations, while OncoMaster.AI uses AI-driven analytics to predict drug responses in colorectal cancer by assessing tumor mutational burden (TMB) and microsatellite instability (MSI). Tumor-informed ctDNA assays monitor minimal residual disease (MRD) via liquid biopsies, offering real-time insights into treatment efficacy and recurrence risk.
Specific Tests
- Cancer Panels (BRCA1/2, hereditary, comprehensive)
- OncoMaster.AI (colorectal cancer)
- Tumor-informed ctDNA assays
Pharmacogenomics

Scientific Description
Studies how genetic variations affect drug metabolism and response. PGx predict individual drug reactions (e.g., warfarin sensitivity), while custom PGx pipelines analyze key enzymes (CYP2D6, CYP2C19) and transporters (SLCO1B1) to optimize dosing and reduce adverse drug reactions (ADRs), which account for ~6.5% of hospital admissions.
Specific Tests
- Polygenic Risk Score (PRS)
- Custom PGx pipelines
Prenatal Screening

Scientific Description
Uses cell-free fetal DNA (cfDNA) from maternal blood to screen for chromosomal abnormalities (e.g., trisomy 21, 18, 13) with >99% accuracy. Advanced NIPT detects microdeletions and single-gene disorders, while genetic counseling integrates genomic data for informed decision-making.
Specific Tests
- NIPT for fetal screening (BASIC & Advanced)
- Prenatal genetic counseling
Rare Disease Diagnosis

Scientific Description
Utilizes clinical-grade next-generation sequencing (NGS) combined with population-specific polygenic risk scores (PRS) to accurately diagnose elusive genetic disorders. Our newborn screening panels employ tandem mass spectrometry to detect inborn errors of metabolism (IEMs), such as phenylketonuria (PKU) and MCAD deficiency, within days of birth. For complex cases, our comprehensive rare disease panels screen for ~5,000 monogenic disorders, incorporating Saudi-specific variant databases to improve diagnostic yield. This approach reduces the diagnostic odyssey from years to weeks, enabling early, targeted interventions for conditions like spinal muscular atrophy (SMN1/SMN2) and lysosomal storage disorders.
Specific Tests
- SMN1/SMN2 screening
- Newborn screening panels
- Rare disease panels
Clinical Research Support

Scientific Description
Multi-omics combines the power of genomics, proteomics, and metabolomics to study biology at multiple levels. It explores the complete DNA sequence to understand genes, analyzes proteins to reveal their functions and interactions, and profiles small molecules (metabolites) to capture the body’s metabolic state. By integrating these layers of information, multi-omics provides a comprehensive view of biological systems, enabling deeper insights into health, disease, and personalized medicine.
Specific Tests
- Microbiome analysis
- Agri-genomics (plants/animals)
- Metagenomics