ClearSeq Inherited Disease Panel
The ClearSeq Inherited Disease, developed in collaboration with Medical Genetics, Charite Berlin, enables focused yet comprehensive mutation profiling of 2742 genes known to cause inherited disorders. It was designed to allow trio analysis on a benchtop sequencer.
This panel is compatible with the SureSelect XT post-capture pooling and XT2 pre-capture pooling as well as the QXT and XTHS library prep and target enrichment solutions,and it features 90-min hybridization. Single analysis and trio analysis are seamlessly supported by the SureCall software.
For Research Use Only. Not for use in diagnostic procedures.