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.
Explore Our Test Menu
We strive to offer a comprehensive and flexible suite of high-quality and affordable genetic testing options coupled with industry-leading TATs, enabling providers and patients to make treatment decisions quicker than ever with results they can trust.
Whole Genome Sequencing
Combining superior coverage of the exome (over 98% covered > 20x) with a six week turn-around time, our Whole Genome Sequencing test is designed to maintain the same quality and TAT that clients deserve from an exome sequencing test, while also providing access to additional valuable information throughout the genome.
Leveraging genomic sequencing technologies and bioinformatics tools, the CNGnome™ test by PerkinElmer Genomics is creating a new standard for detecting large copy number changes (CNV) throughout the genome.
Our AnyPanel test gives clients access to thousands of genes and panel combinations to tailor testing specifically to each patient’s needs. When ordering AnyPanel, you can either chose from a list of over 200 expertly-curated panels OR create your own panel simply by submitting the list of genes that you would like analyzed.
With over 7 million babies screened globally since 1994, PerkinElmer Genomics is one of the largest independent newborn screening programs in the world. With a menu ranging from single biochemical screening tests to large newborn screening genetic testing panels, we strive to be a one-stop-solution for all of your newborn screening needs.
Built on our pillars of confidence, acceleration, and accessibility, this program is designed to bring providers the high-quality genetic tests that they demand, but at prices that they are not accustomed to seeing!