Many needs. One sure solution.
The SureSelectXT HS product family is Agilent's state-of-the-art library prep and target enrichment solution. It offers a fast, streamlined and highly sensitive workflow. You can use small amounts of FFPE DNA as input and detect allele frequency down to 1% or lower, making it a great tool for cancer research. With the advanced new features, it could satisfy most, if not all, of your needs for NGS sample preparation.
The SureSelectXT HS product family can be used with both catalog and custom NGS panels. Custom panels can be designed in SureDesign, a free web-based design portal that makes panel design fast and easy.
"One of the best kits we have tested out of the box."
"This customizable target enrichment technology, with integrated molecular barcode error correction, enables us to detect ultra-low mutation frequencies in very small DNA quantities. This makes it ideal for the detection and tracking of clonal and subclonal variants in liquid biopsies."