New Retina subpanels

CeGaT introduces three additional Subpanels for Hereditary Eye Diseases:

  • Stargardt disease and macular dystrophies (11 Genes)
  • Cone rod dystrophies (25 Genes)
  • Flecked retina disorders (6 Genes)

We are now offering 32 Subpanels:

  • Dementia and ALS (1 Subpanel – 20 Genes)
  • Parkinson Syndrome (1 Subpanel – 16 Genes)
  • Epilepsy (15 Subpanels – 265 Genes)
  • Hereditary Eye Diseases (15 Subpanels – 196 Genes)

For further information please visit our Diagnostic Panels section.

New Epilepsy subpanels

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.

Introduction of Diagnostic Panels

CeGaT is among the worldwide pioneers and the first German company introducing Diagnostic Panels.
With our panels a high number of genes can be sequenced and diagnosed simultaneously. In total we offer 16 different subpanels:

  • Dementia and ALS (1 Subpanel, 20 Genes)
  • Parkinson Syndrome (1 Subpanel, 16 Genes)
  • Epilepsy (3 Subpanels – 55 Genes)
  • Hereditary Eye Diseases (11 Subpanels, 150 Genes)

For further information please visit the Diagnostic Panels section.