Celemics - Model CES - G-Mendeliome Clinical Exome Sequencing Panel

The CES is a widely used diagnostic method to rapidly and efficiently detect disease-causing genetic variations within target genes in the human genome. The G-Mendeliome CES Panel includes both clinically significant genes used in other panels and other additional genes, therefore allowing customers to obtain comprehensive information of mutations in genes of interest in a cost-effective manner.

Comprehensive genomic profiling of a variety of genetic diseases

• Includes 7,000 genes associated with clinically significant genetic diseases

A wide range of target regions

• Includes all clinically significant regions that are not covered by competitor`s panels

Cost-effective analysis

• Able to provide accurate analysis with reduced sequencing costs compared to WES