Our areas of specialty include:

Newborn Screening Genetic Testing Whole Genome Sequencing Whole Exome Sequencing

PerkinElmer Genetics has a long history and is dedicated to improving the lives of families by offering early detection of inherited disorders. As one of the world’s largest providers of newborn screening services, we have decades of experience in screening for complex rare diseases. With over six million babies screened globally since 1994, PerkinElmer Genetics helps save the lives of thousands of babies every year.

We are proud to continue the tradition by offering clinical genetic services to help provide a continuum of care for our patients and clinicians. PerkinElmer Genetics offers comprehensive genetic testing solutions that will help provide insight into the complex nature of rare and inherited diseases.

Quick Links

For Clinicians

PerkinElmer Genetics is a global leader in providing screening and diagnostic testing for rare and inherited diseases. We are a provider who combines high-volume screening with diagnostic genetic testing.

Learn about our Institutional Advantage Program designed to bring providers the high-quality genetic tests that they demand, but at prices that they are not accustomed to seeing! Learn More

For Patients and Parents

Patients and Parents suffering from complex rare genetic diseases often have limited places to turn for testing and treatments. PerkinElmer Genetics helps turn the complex nature of the disease into more understanding by providing meaningful and actionable genetic test results.

For Pharma

Our goal is to help pharmaceutical and biotech companies in successful drug development and commercialization by providing diagnostic testing solutions.
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