Identify Pathogenic Variants Across the Exome
Mapping Your Protein-Coding Genome for Precise Genetic Insights
DNA GTx’s Whole Exome Sequencing (WES) analyzes all protein-coding regions (the exome) of the genome to detect genetic mutations that may cause or contribute to disease. This comprehensive panel supports accurate diagnosis, disease risk assessment, and personalized treatment planning, offering more targeted approach.
Who is this Test for?
- Individuals with undiagnosed genetic conditions
- Patients with complex diseases
- People with a strong family history of inherited disorders
- Children or adults with developmental delays, neurological symptoms
What it screens for?
- Undiagnosed conditions
- Hereditary cancer syndromes
- Neurological, metabolic, and developmental diseases
Variant Types Detected
Single Nucleotide Variants (SNVs)
- SNVs are single base changes between reference and the patient's genome.
Insertions and Deletions (Indels)
Insertion
Deletion
- Indels are small changes in DNA where a few bases are either added (insertion) or removed (deletion).
Copy Number Variants (CNVs)
Amplification / Duplication
Deletion
- Parts of DNA that are copied too many times or missing.
Key Benefits
- Comprehensive Genetic Insight: Covers ~20,000 genes to identify disease-causing mutations.
- Supports Accurate Diagnosis: Helps uncover the genetic basis of complex conditions.
- Enables Personalized Care: Guides targeted treatment and long-term health management.
- Broad Clinical Utility: Applicable across multiple specialties, from oncology to pediatrics.
Turn Around Time
- 4-5 weeks
Do You Need a Doctor’s Request?
A doctor must request this test. They will review your medical history and symptoms to determine if WES is appropriate and will help you understand the results.
How it Works?
Step 1: Blood Sample Collection
- A blood draw is taken from the patient.
- The sample contains DNA that can reveal important health insights.
Step 2: DNA Extraction
- We carefully extract the DNA from the sample.
- This DNA is what we need to study your genes.
Step 3: Library Preparation
- The DNA is prepared so it can be read by our sequencing machines.
- We add special tags and focus on the most important parts of your DNA.
Step 4: Next Generation Sequencing
- This is how we ‘’read’’ your DNA using advanced technology.
- It helps us find changes or mutations in your genes.
Step 5: Data Analysis
- Our proprietary software (D-KRYPT) helps us understand what the DNA changes mean.
- The results are derived from trusted medical databases.
Step 6: Personalized Patient Report
- You got a clear, easy-to-read report with important findings.
- Your doctor can use this to guide treatment or next steps.
Oncology Test Panels
Séquençage clinique
Solutions for Researchers
Prise en charge prénatale
Médecine régénérative
Healthcare
Agriculture
Let’s Decode the Future of Health — Together
Get in touch today — let’s start a conversation that could change lives
*All information is handled with strict confidentiality.
Find Answers Today
Early detection saves lives
*All information is handled with strict confidentiality.
