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
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.
Knowledge to Empower Health