The whole-exome sequencing test is an in-house developed test that integrates over 1000 clinically significant SN and InDel hotspot mutation sites with internal and public databases. With no more than 100 ng DNA input, the limit of detection (LoD) is 6% for SNV, InDel, and fusion callings.
Product Introduction
1000+ Hotspot Mutation
Based on Burning Rock internal database & public database, integrate common 1000+ clinically significant SN/InDel hotspot mutation sites
Fusion: 21 Genes
Under 100ng DNA input, LoD for calling fusion mutation is 6%
Non-hotspot SNV&InDel
Under 100ng DNA input, LoD for calling SNV&InDels mutation is 6%
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