Full-Spectrum Genetic Testing for Personalized Care
Explore the Complete View of Your Genetic Code
DNA GTx’s Whole Genome Sequencing (WGS) analyzes the entire DNA sequence, covering both coding and non-coding regions of the genome. This comprehensive approach detects a wide array of genetic variants, enabling precise diagnosis and personalized treatment plans, especially valuable for rare diseases and unexplained clinical presentations.
Who is this Test for?
- Individuals with undiagnosed or rare diseases, especially when other tests haven’t provided answers
- Patients with a complex medical history or unclear genetic cause
- Patients with unexplained clinical presentations
- Families seeking a comprehensive genetic risk profile
- Researchers and specialists looking for deeper genomic insights
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.
Mitochondrial DNA
- Mitochondria are the “powerhouse” of the cell, and they have their own small set of DNA. Changes in this DNA can affect how cells make and use energy, sometimes helping cancer grow.
What it Screens for
- Genetic variants across the entire genome, including:
- Coding regions (exons)
- Non-coding regions (introns, promoters, regulatory elements)
- Linked to:
- Rare and undiagnosed genetic disorders
- Hereditary diseases
- Structural variants and copy number changes
- Complex and multi-system conditions
Key Benefits
- Most Comprehensive Genetic Test: Covers both coding and non-coding regions of DNA.
- Detects All Variant Types: Identifies SNVs, indels, CNVs, structural variants, and more.
- Supports Complex Diagnoses: Ideal for cases with unclear or elusive genetic causes.
- Enables Precision Medicine: Guides diagnosis, treatment, and long-term care planning.
Turn Around Time
- 4-5 weeks
Do You Need a Doctor’s Request?
Yes. A healthcare provider must request the test. They’ll help determine if WGS is appropriate based on your medical history and will guide you through 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.
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Séquençage clinique
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*All information is handled with strict confidentiality.
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Early detection saves lives
*All information is handled with strict confidentiality.
