Expand your capabilities
Carrier screening
Preimplantation testing
Preimplantation research
Newborn screening
Sexual health testing

 

 

Research testing solutions

What is carrier screening research?

In today’s multiethnic society, some genetic disorders previously thought to be confined to specific ethnic groups are increasingly being found in broader populations. Next-generation sequencing (NGS) enables rapid carrier screening research across the broadest range of disorders, crossing ancestries and geographic regions, with a scalable, cost-effective solution.

 

Interactive eBook series: Decoding carrier screening

Part 1: Expanding horizons in reproductive health

Part 1: Expanding horizons in reproductive health

Learn about:

  • Carrier screening, expanded carrier screening, and the importance of screening early
  • Important questions raised with new screening technologies
  • Expanded carrier screening best practices
Part 2: Evolving methods for genetic testing

Part 2: Evolving methods for genetic testing

Learn about:

  • Evolving analytical methods in carrier screening
  • Genetic variants commonly tested in carrier screening
  • Three main genetic testing methodologies, with a focus on molecular analysis
Part 3: Putting expanded carrier screening into practice

Part 3: Putting expanded carrier screening into practice

Learn about:

  • Choosing an expanded carrier screening approach
  • Basic workflow steps: sample collection and preparation, genetic testing, and data analysis
  • Deciding what to report and understanding outcomes

Download eBooks

Discover our workflow

Prepare your sample

Resources

Analyse your sample

Resources

Expand your capabilities for reproductive health genetic testing

Expand your capabilities for reproductive health genetic testing
 

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For Research Use Only. Not for use in diagnostic procedures.

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