Advanced Genomics Platform

Novagen Testing for a Healthier, Stronger Future

We combine advanced technology with medical expertise to deliver cutting-edge diagnostic solutions — empowering better healthcare decisions through early detection, accurate analysis, and actionable results.

665K+
Genomes Analyzed
20K+
Genes Covered
99.2%
Accuracy Rate
Live Genomic Analysis
Overview
● Active
Samples Today
1,284
↑ 12% vs yesterday
Pending Reports
47
→ In processing
Exome Coverage Distribution
🧬 WES Active 📊 AI Insights On
Next-Generation Sequencing
Whole Exome Sequencing
Genomic Variant Analysis
Clinical Interpretation
AI-Powered Insights
Fast Turnaround Time
Comprehensive Reporting
Research & Development
Quality Assurance
Expert Consultation

Empowering Healthcare Through Innovation

Streamline your operations and elevate patient outcomes with our comprehensive suite of genomic and clinical testing tools. We bring clarity and confidence to every diagnosis.

Are You a Provider?


Accelerate diagnosis and personalize treatment with our next-generation exome and genome sequencing. Designed for precision and speed, our technology supports healthcare providers in delivering patient-centered care across all age groups.

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Looking for a Diagnosis?


Our comprehensive exome testing analyzes over 20,000 genes, helping reveal the root cause of complex conditions. Gain faster insights that guide better treatment decisions and long-term health management.

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Interested in Testing?


Take control of your health with our easy-to-use testing kits. Receive accurate, physician-backed results from the comfort of your home and uncover genetic insights that help you make informed lifestyle and medical choices.

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Accelerating Accurate Diagnoses — we envision a future where genetic disorders are identified early, allowing proactive treatment and healthier lives.

Through advanced exome and whole-genome sequencing, we provide critical insights for each person. Every test brings us closer to making precision medicine accessible for everyone.

Our Story
665K+
Genomes
Completed
🏆
HIPAA Compliant
Enterprise-grade data security & privacy

Advancing Genetic Discovery with Exome Sequencing

Empower your patients with faster, more accurate genetic diagnoses. Our sequencing solutions redefine what's possible in genomic testing, delivering lifetime insights from a single DNA sequence.

  • 1
    Up to 5× More Accurate. Whole Exome Sequencing (WES) is up to 5× more accurate than conventional methods and can detect chromosomal abnormalities unidentifiable by other means.
  • 2
    Comprehensive Coverage. 1 in 5 newborns in neonatal intensive care may have a detectable genetic condition, identifiable through whole genome sequencing.
  • 3
    Lifetime Value. A single exome test can have a valuable genetic record that may provide insights throughout a person's entire life.
See How It Works →
Novagen Genomics Dashboard
Coverage
98.7%
Variants Found
4,281
↑ 231 pathogenic
Report Ready
72hr
avg turnaround
CHROMOSOME COVERAGE MAP
Sample QC Passed — High Quality
Sample ID: NGL-20250328-4821

Complete Genomic Care, From Start to Finish

We don't just provide results — we deliver end-to-end genomic support. With more than 665,000 exome and genome analyses completed, our expertise spans pediatric and rare genetic disorders.

  • 1
    Complex Data Made Clear. Our specialists translate complex data into clear, actionable insights, supported by certified genetic counselors throughout testing and interpretation.
  • 2
    Certified Counselors. Certified genetic counselors who guide patients and providers through every stage of testing and care planning.
See How It Works →
GENETIC COUNSELOR CHAT
Hi! Your exome results are ready. No pathogenic variants were found — great news! 🎉
Thank you! Does this rule out hereditary cancer risk?
It significantly reduces risk for the 50+ genes we screened. I'll schedule a detailed debrief call.
That would be perfect. What time works?
👩‍⚕️
Dr. Sarah is typing…

Leaders in Precision Medicine

Delivering better health outcomes through advanced genomic diagnostics.

1
Actionable Insights for Smarter Care

Our interactive platform transforms genetic data into clinically relevant charts, supporting genome diagnosis, personalised treatment, and improved patient outcomes.

2
Simplified Genetic Testing

Experience genetic testing with easy-to-understand results. Parents can easily collect samples at home and receive physician-reviewed results that inform long-term health management.

3
Genetics and Preventive Health

Since genetics influence 6 of the 10 leading causes of death, we help identify risk for heart disease, cancer, diabetes, and more, empowering proactive prevention.

4
Enhancing Clinical Decision-Making

Our certified specialists provide insights that help clinicians make informed treatment plans with confidence and precision.

5
Beyond Results: Delivering Understanding

We translate raw results into meaningful insights that connect patients to targeted therapies and accelerate research-driven solutions.

🧬
Precision Genomics
at Your Fingertips
Advanced analysis tools for clinicians and genetic counselors
WES Analysis CNV Detection AI Reports

Frequently Asked Questions

Find answers to common questions about Avintis Diagnostics

Most implementations take 2–4 weeks, depending on your existing systems. Our dedicated team ensures a seamless transition with complete staff training.

Yes. We adhere to strict privacy and security protocols to protect patient data and maintain full HIPAA compliance.

Absolutely. Our platform is built for seamless integration with most major EHR and LIMS systems.

Yes. We provide customized reports tailored to your practice needs, helping you focus on what matters most patient care.

Our clinical support team and genetic counselors are available to assist before, during, and after testing, ensuring your patients and staff receive continuous guidance and care.