CeGaT introduced 15 Epilepsy Subpanels. With these Diagnostic Panels all genes associated with Epilepsy can be sequenced simultaneously on our SOLiD 4 platform. We offer a full Epilepsy Diagnostic (Sequencing on SOLiD 4 system, Data Analysis, Re-Sequencing of Variants, Report) for each of our subpanels.
We are now offering 28 subpanels:
- Dementia and ALS (1 Panel – 20 genes)
- Parkinson Syndrome (1 Panel – 16 genes)
- Epilepsy (15 Panels – 265 genes)
- Hereditary Eye Diseases (11 Panels – 168 genes)
For further information please visit the Diagnostic Panels section.