Agilent Technologies, Inc. - Diagnostics and Genomics ClearSeq Inherited Disease, 16, XT
The Agilent ClearSeq Inherited Disease, 16, XT (part number 5190-7518) is a targeted next-generation sequencing (NGS) panel designed for the detection of inherited disease-associated variants. This panel enables comprehensive analysis of genes implicated in a wide range of inherited disorders, supporting clinical research and genetic studies. The kit is optimized for use with Agilent's SureSelect target enrichment system, providing high specificity and uniform coverage. It is suitable for processing 16 samples and is compatible with Illumina sequencing platforms, facilitating streamlined workflows for laboratories focused on inherited disease research.