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The ClearSeq Inherited Disease enables analysis of 2,742 genes known to cause inherited disorders.
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.
ClearSeq Inherited Disease Data Sheet
| Chinese (Simplified) (China) | Complete (PDF) |
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This application note describes the conversion of a typical GC/MS method for the qualitative analysis of flavor and fragrance compounds in essential oils from helium to hydrogen.