Our Areas of Expertise

Pairing our decades of experience in maternal, fetal and newborn screening with a state-of-the-art clinical genomics program, PerkinElmer Genomics provides one of the world’s most comprehensive programs for detecting clinically significant genomic changes. Our high-quality, fast, affordable results allow clinicians to offer patients the answers they need to determine their path forward.

Who We Serve

SERVING

Healthcare Providers

At PerkinElmer Genomics, patients and healthcare providers are at the heart of what we do. We believe that genetic testing is a deep-rooted partnership, and are committed to making it accessible and meaningful to the patients and families we serve around the world.

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SERVING

Patients & Parents

PerkinElmer Genomics pairs decades of newborn screening experience with a leading-edge clinical genomics program to offer one of the world’s most comprehensive programs for detecting clinically significant genomic changes. Working together with physicians, PerkinElmer Genomics aims to deliver knowledge that can empower health.

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SERVING

Pharma & Research

PerkinElmer Genomics has a long history of screening and identifying patients with rare diseases.  Since our founding in 1994, we have screened more than 7 million newborns. We help save the lives of thousands of babies every year.

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Knowledge to Empower Health

Learn more about PerkinElmer Genomics

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