Developed in collaboration with researchers from Medical Genetics, Charite Berlin, this panel is a highly targeted design that enables comprehensive analysis of only those 2,742 genes known to cause inherited disorders. Faster time to sequencing is achieved when coupled with efficient SureSelect workflows that enable greatly reduced hybridization times. Deeper coverage of targets, whether single samples or trios even on a benchtop sequencer, accelerates answers with confident variant calling enabled by SureCall, a guided data analysis solution from raw data to categorized variants.
Compatible with SureSelect Target Enrichment System
A highly targeted design that enables comprehensive analysis of only those 2,742 genes known to cause inherited disordersCompatible with SureSelect,XT and XT2
貨號 | 產品 | 數量 | |
---|---|---|---|
5190-7518 | ClearSeq Inherited Disease, XT | 16 rxns | |
5190-7519 | ClearSeq Inherited Disease, XT | 96 rxns | |
5190-7520 | ClearSeq Inherited Disease, XT | 96 rxns Auto | |
5190-7521 | ClearSeq Inherited Disease Plus, XT | 16 rxns | |
5190-7522 | ClearSeq Inherited Disease Plus, XT | 96 rxns | |
5190-7523 | ClearSeq Inherited Disease Plus, XT | 96 rxns Auto | |
5190-7524 | ClearSeq Inherited Disease, XT2 | 16 rxns | |
5190-7525 | ClearSeq Inherited Disease, XT2 | 96 rxns | |
5190-7526 | ClearSeq Inherited Disease, XT2 | 96 rxns Auto | |
5190-7527 | ClearSeq Inherited Disease Plus, XT2 | 16 rxns | |
5190-7528 | ClearSeq Inherited Disease Plus, XT2 | 96 rxns | |
5190-7529 | ClearSeq Inherited Disease Plus, XT2 | 96 rxns Auto |