Whole-exome sequencing (WES) specifically targets thousands of protein-coding regions of the genome, offering an affordable and efficient approach for detecting rare genetic variants and discovering disease biomarkers. To identify the relevant genetic variations contributing to a phenotype and symptoms, researchers employ software solutions, such as QCI Interpret Translational, to simplify and accelerate the genomics data analysis process by eliminating manual curation.
Download this application note from QIAGEN to learn about a robust WES workflow for rapid variant annotation, filtering, and triage.
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