Providing Comprehensive Screening and Diagnostic Testing
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.
Leveraging PerkinElmer’s position as an industry-leader in work-flow solutions and genetic expertise, we create unmatched efficiency, quality, and sustainability within the lab. These capabilities enable us to accelerate our report delivery and increase affordability empowering clinicians and researchers to utilize genetic testing earlier in the diagnostic process.
With a network of laboratories in China, India and USA, PerkinElmer Genomics can support research and testing collaborations around the globe. Our collaborators can access capabilities such as:
Sample Collection and Logistics
Collection packet design, manufacturing and distribution
Ability to support testing on different sample types: Dried blood spots (DBS), Saliva (SV), Whole blood (WB)
Microsampling with DBS provides convenient and inexpensive sample transportation
Clinical Grade Custom Assay Development and Testing Service Programs
PerkinElmer Genomics can build customized assays to the appropriate technology
Expertise in utilizing DBS for Mass spectrometry metabolites, Enzyme activity, Next Generation Sequencing, Nucleic acid analysis, and Immunoassays
Develop customized testing service programs in support of our collaborators’ clinical research needs
Versatile Delivery Models
Full service testing services via our network of clinically CAP certified global testing labs
Lab in Lab model
Customer contracted manufacturing services
Experience in Genomics
PerkinElmer Genomics has extensive experience in genomics via our team of certified Biochemical Genetics, Cytogenetics and Molecular Genetics experts.
PerkinElmer Genomics offers a wide array of services to pharmaceutical companies and researchers who are in need of screening patients for genetic diseases. We enable research and testing service programs to deploy globally through our network of labs and our enhanced access to testing.
Our AnyPanel™ test gives clients access to thousands of genes and panel combinations to tailor testing specifically to each patient’s needs. When ordering the AnyPanel™ test, 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.
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.
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.
Pursuant to applicable federal and/or state laboratory requirements, PerkinElmer Genomics has established and verified the accuracy and precision of its testing services. Tests are developed and performance characteristics determined by PerkinElmer Genomics.