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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.
- Easily reflex to Whole Exome Sequencing if your initial panel does not find a cause of disease.
- 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 |
| 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
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.