| This is a highly targeted design that enables analysis of only the disease-associated targets. It provides deep coverage even on a benchtop sequencer. It shows 20 or more reads for 95% of targets at 1.5 Gb (100x) of sequencing and 98% of targets with 3 Gb (200x) of sequencing. This enables the coverage of disease-associated regions. Even when sequenced on benchtop sequencers, the panel facilitates sensitive and accurate variant calling, reducing time to answers. |
| The kit enables targeted analysis of only those regions that have previously been associated with disease linked to HGMD, OMIM, and ClinVar. When compared with similar solutions, the optimized panel design coupled with SureSelect technology, provide a single assay, allowing interrogation of disease-associated regions for a comprehensive analysis of sample. This makes it suited for the study of rare idiopathic disorders. Addition of custom content using SureDesign lets you tailor this panel to meet your specific design requirements. |
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SureSelect Focused Exome is compatible with SureSelectQXT, a target enrichment workflow that enables 3.5x faster workflow compared to competing solutions. This solution enables an efficient workflow from sample-to-sequencing reducing turn-around time while providing confident variant calling. Targeted analysis using SureCall provides guided workflows for single or trio analysis of samples enables facilitated identification of SNPs, indels as well as CNVs. Hotspot analysis is enabled through the known variants workflow, enabling locus-specific detection of variants. |
