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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.

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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
  • Family targeted carrier testing 

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 
Visit Our Online Ordering Portal

CentoPortal® is a user-friendly, online, web-based ordering portal designed to assist you at every step of processing your patients’ samples.

We Are Here to Guide

Our global network of customer support and experts guiding you every step of the way.

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