Whole exome sequencing (WES) is a powerful genetic technique that targets and analyzes the protein-coding regions of an individual’s genome, known as the exome. While the exome represents only a small fraction of the total genome, encompassing approximately 1 to 2% of DNA, it contains the majority of known disease-causing mutations. <a href=”https://bioaro.com/wholeexome”><b>whole exome sequencing</b></a> offers a cost-effective and efficient approach to uncovering genetic variations that may contribute to a wide range of inherited disorders and complex diseases.
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