About AnyGene™

We harness our next-generation sequencing technology for focused, diagnostic single-gene testing with deletion/duplication analysis. Our AnyGene™ test gives you access to thousands of genes so you can find the right fit for your patient.

The PerkinElmer Genomics Difference

  • Choose from thousands of disease-associated genes to tailor your custom single gene test to your patients’ testing needs.
  • Enhanced NGS coverage with powerful bioinformatics to detect the majority of copy number variants (CNVs) at least 3 exons in size.  Although smaller CNV events may also be detected and reported, additional follow-up testing is recommended if a smaller CNV is suspected.
  • Average turn-around-time of 3-5 weeks and STAT options available with a TAT of 7 to 10 days. 
  • Flexible convenience with multiple sample types,  including saliva swabs, dried blood spots, whole blood, and genomic DNA. 
Order Testing

Popular AnyGene™ Links

Select a Gene

Test Resources

Requisition Form – AnyGene™
Exome and Panel Coverage Tool

How to Order

1. Select Your
Custom Gene


2. Complete and print the test requisition


3. Collect and Send Patient Sample


AnyGene™ Test FAQs

The AnyGene™ test options have an average turn-around-time of 3-5 weeks. STAT testing is also available to accelerate the delivery of results to patient with a TAT of 7-10 days.

Panels include NGS-based capture with no additional assays or pseudogene testing.

For pricing, please email PerkinElmer Genomics or call us at 1-866-354-2910.

PerkinElmer Genomics accepts multiple sample types including Saliva Swabs, Dried Blood Spots, Whole Blood, and Genomic DNA.

Yes, you can opt to ship testing kits directly to patients in our online ordering portal. Find out more about the process here.

All reported variants are confirmed using an orthogonal method.

PerkinElmer Genomics follows the published ACMG guidelines when classifying identified variants.

Contact PerkinElmer Genomics for more information