Next-generation sequencing is an efficient and highly parallel way of screening thousands of targets for disease-causing genes. Whole exome sequencing analysis takes it a step further by focusing on the coding regions of the genome that harbor >85% of disease variants.
Our extensive range of QIAseq whole exome sequencing kits delivers exceptional coverage uniformity, no matter the GC composition of your target. Additionally, the kits facilitate >99% base level coverage of targets at ≥20x, drive comprehensive and sensitive detection of variants (>98% combined sensitivity for SNVs and Indels) and minimize drop-outs. The sample to sequencing workflow reduces your sequencing costs by up to 50% and is at least 33% faster than other exome workflows.