CeGaT Panel for Epilepsy, Metabolic and Brain Development Disorders
The panel for hereditary Epilepsy, Metabolic and Brain Development Disorders covers 670 genes. All of these genes are sequenced simultaneously. Only genes which have an association with the phenotype of the patient will be interpreted. Below, next to all genes of the panel, you can find our proposed gene sets.
For diagnostic purposes, each of the gene sets can be requested individually or in combination. A combination of individual genes is also possible.
Should you have any questions please do not hesitate to contact our Diagnostic Support team.
The enrichment of the coding regions and the adjacent intronic regions is performed using the in-Solution Agilent technology (SureSelectXT). The selection of the targeted regions and the design of the enrichment baits is performed in-house.
High throughput sequencing is performed on the Illumina HiSeq Platform.
Bioinformatic processing of the data is achieved using an in-house computer cluster.
Following data processing, our team of scientists and specialists in human genetics analyze the data and issue a medical report.
Material and turnaround time
3-5 ml EDTA-Blood or 5 µg genomic DNA
Order form with declaration of consent according to German Gendiagnostikgesetz (GenDG)