Agilent Technologies, Inc. - Diagnostics and Genomics ClearSeq Inherited Disease, 96, XT
The Agilent ClearSeq Inherited Disease, 96, XT (part number 5190-7519) is a targeted next-generation sequencing (NGS) panel designed for the detection of inherited disease-associated variants. This product enables comprehensive analysis of genes implicated in a wide range of inherited disorders, supporting clinical research and genetic testing applications. The kit is optimized for use with Agilent's SureSelect target enrichment system and provides high sensitivity and specificity for variant detection. It is supplied in a 96-reaction format, facilitating high-throughput workflows in clinical genomics laboratories.