Single Genes
Many genetic diseases are caused by changes or variants in a single gene. We offer a comprehensive range of tests for myriad single gene disorders.
Single Genes
The type of test method required depends on the type of change that causes the disorder.
- Sanger sequencing for hotspot analysis and single gene sequencing
- Next generation sequencing (NGS) for single gene sequencing and NGS-based copy number variation (CNV) analysis
- Deletion/duplication testing to identify large deletions or duplications using MLPA (multiplex ligation-dependent probe amplification) or qPCR (real-time polymerase chain reaction)
- Fragment length analysis (FLA) and/or repeat primed assays (RPA) to detect the extent of the repeat expansions using a capillary sequencer
Single Gene Testing Is Recommended for Patients With
- Distinctive clinical features
- Family history of a specific disorder
- Single gene disorders
- Possible epigenetic disorder
- Possible Triple repeat disorders
- Family targeted carrier testing
how it works
Book in Clinic or Home
Visit or We’ll Visit You: Start your journey either by visiting our clinic or opting for our convenient home collection service.
FDA Approved Laboratory
Global Laboratory Analysis: Your sample is sent to one of the world’s leading laboratories, ensuring top-notch accuracy and reliability.
Personalized Health Plan
Comprehensive Insights: Within 10 days, receive your detailed genetic report and Free Consultation. Your path to personalized health insights begins here.
CONTACT US
If you have a query, no matter how small or significant we’ll do our best to assist you. You can call us using the number provided or open a Live Chat with one of our agents.
