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The PerkinElmer Genomics Difference

  • Enhanced NGS coverage with powerful bioinformatics to detect the majority of copy number variants (CNVs) at least 3 exons in size. 
  • One of the fastest average turn-around-times at 3 weeks or less 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.

Cardiology Testing Options

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

Test Code Test Name Turn Around Time
D4100 Arrhythmogenic Cardiomyopathy Panel

24 Genes

3-5 weeks Learn More
D4101 Comprehensive Cardiomyopathy Panel

122 Genes

3-5 weeks Learn More
D4102 Dilated Cardiomyopathy Panel

69 Genes

3-5 weeks Learn More
D4103 Hypertrophic Cardiomyopathy Panel

60 Genes

3-5 weeks Learn More
D4104 Sudden Cardiac Arrest (SCA) Panel

11 Genes

3-5 weeks Learn More
D4105 Arrhythmia Comprehensive Panel

73 Genes

3-5 weeks Learn More
D4106 Long QT Syndrome Panel

17 Genes

3-5 weeks Learn More
D4107 Short QT Syndrome Panel

6 Genes

3-5 weeks Learn More
D4108 Brugada Syndrome Panel

9 Genes

3-5 weeks Learn More
D4109 Cardiomyopathy and Skeletal Muscle Disease Panel

158 Genes

3-5 weeks Learn More
D4110 Marfan/TAAD Panel

23 Genes

3-5 weeks Learn More
D5086 Familial Hypercholesterolemia Panel

3 Genes

3-5 weeks Learn More
D5087 APOB Gene Test

1 Genes

3-5 weeks Learn More
D5088 LDLR Gene Test

1 Genes

3-5 weeks Learn More
D5089 PCSK9 Gene Test

1 Genes

3-5 weeks Learn More
Prioritized NGS-based testing with accelerated turn-around-times of 7 to 10 days.

Test Code Test Name Turn Around Time
D4101F STAT Comprehensive Cardiomyopathy Panel

122 Genes

7 -10 days Learn More
D4100F STAT Arrhythmogenic Cardiomyopathy Panel

24 Genes

7 -10 days Learn More
D4102F STAT Dilated Cardiomyopathy Panel

69 Genes

7 -10 days Learn More
D4103F STAT Hypertrophic Cardiomyopathy Panel

60 Genes

7 -10 days Learn More
D4104F STAT Sudden Cardiac Arrest (SCA) Panel

11 Genes

7 -10 days Learn More
D4105F STAT Arrhythmia Comprehensive Panel

73 Genes

7 -10 days Learn More
D4106F STAT Long QT Syndrome Panel

17 Genes

7 -10 days Learn More
D4107F STAT Short QT Syndrome Panel

6 Genes

7 -10 days Learn More
D4108F STAT Brugada Syndrome Panel

9 Genes

7 -10 days Learn More
D4109F STAT Cardiomyopathy and Skeletal Muscle Disease Panel

158 Genes

7 -10 days Learn More
D4110F STAT Marfan/TAAD Panel

23 Genes

7 -10 days Learn More
D5086F STAT Familial Hypercholesterolemia Panel

3 Genes

7 -10 days Learn More
D5087F STAT APOB Gene Test

1 Genes

7 -10 days Learn More
D5088F STAT LDLR Gene Test

1 Genes

7 -10 days Learn More
D5089F STAT PCSK9 Gene Test

1 Genes

7 -10 days Learn More

How to Order

1. Complete & print the test requisition below.

Ensure that:

  •      All sections are complete
  •      You have the correct test code
  •      Your patient has signed an informed consent

2. Collect patient sample.

Obtain a sample for testing from the patient and confirm that the sample is correctly labeled with the patient’s name and date of birth

Note: if you do not have a PerkinElmer Genomics kit available in your office, please email or call us at 1-866-354-2910.

3. Send patient sample.

Ship your test kit back using the pre-paid shipping label. Remember to include:

✔   Patient sample

✔   Completed informed consent

✔   Test requisition form

✔   Any applicable medical records or clinical notes

Requisition Form – Panel Testing

FAQs

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

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

No, all Cardiology tests are the same cost regardless of the number of genes ordered.

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.

The genes on our pre-curated panels were chosen by our expert team of board-certified geneticists based on the clinical indication of the test and the genes’ association with disease.

Yes, a full list of pre-curated panels can be found here.

For questions about gene coverage, please email PerkinElmer Genomics or call us at 1-866-354-2910.

If you have additional questions, please feel free to email or call us at 1-866-354-2910.