NGS Exome Probes offer excellent coverage of targeted regions with minimal exome sequencing.
NGS Exome Probes offer the depth and breadth of coverage you need for discovering mutations associated with diseases. It includes SureSelect Human Exomes, Clinical Research Exomes, Animal Exomes and exomes that can be customized. Agilent Exome probes offer streamlined solutions enabling high-throughput and work Next-Generation Sequencing Applications. Agilent Whole Exome Sequencing (WES) is a very effective approach for discovering the causal mutation for inherited diseases. Exome sequencing identifies variants across a wide range of applications, achieves comprehensive coverage of coding regions, provides a cost-effective alternative to whole-genome sequencing. Also, it produces a smaller, more manageable data set for faster, easier analysis compared to whole-genome approaches.