RNA Sequencing for Detecting Gene Fusions and Transcript Variants
Decoding the Transcriptome for Deeper Biological Insights
DNA GTx's RNA sequencing analyzes gene expression and detects gene fusions, splicing variants, and mutation. This comprehensive transcriptomic profiling provides critical insights into disease mechanisms, tumor biology, and supports precise treatment guidance.
What it Screens for
- Cancer profiling
- Rare genetic diseases
- Neurological and metabolic conditions
Key Benefits
- Reveals Gene Activity: Analyzes how genes are expressed and regulated.
- Detects Fusions and Splicing Events: Uncovers alterations not visible through DNA testing.
- Complements DNA Sequencing: Provides additional insights into disease mechanisms.
- Guides Targeted Therapy: Supports treatment decisions, especially in oncology.
Turn Around Time
- 5-6 weeks
How it Works?
Step 1: Blood Sample Collection
- A blood draw is taken from the patient.
- The sample contains RNA that can reveal important health insights.
Step 2: RNA Extraction and Enrichment
- RNA is carefully isolated and enriched form the blood sample.
- This ensures the RNA is of high quality and ready for sequencing.
Step 3: Next Generation Sequencing
- This is how we ‘’read’’ your RNA using advanced technology.
- It helps us find changes or mutations in your genes.
Step 4: Data Analysis
- Our proprietary software (D-KRYPT) helps us understand what the RNA changes mean.
- The results are derived from trusted medical databases.
Step 5: 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
Clinical Sequencing
Solutions for Researchers
Prenatal Care
Regenerative Medicine
Healthcare
Agriculture
Let’s Decode the Future of Health — Together
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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.
