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必威体育登录手机Optimization of an Agilent NGS Automated Workflow for the Characterization of NSCLC DNA Samples in a Molecular Diagnostic and Anatomic Pathology Laboratory
"Many types of cancers are caused by either inherited or de novo genomic abnormalities such as single-nucleotide variants (SNVs), copy number variations (CNVs), and/or chromosomal translocations."
Brochure on SureSelect Cancer All-In-One Catalog and Custom Assays
Overview of the SureSelect Cancer All-In-One workflow
SureSelect Cancer All-in-One solid tumor assay enables the detection of SNVs, indels, CNVs and translocations in genes relevant to common tumor types.This assay requires a single genomic DNA and is compatible with FFPE tumor samples.
必威体育登录手机Agilent community designs are NGS panels and microarrays created by our customers and deployed successfully in their laboratories and are now available to you.
One assay, all lung cancer-relevant variants in a single DNA workflow
SureSelect NGS Panels: Customized for Any Application
"With the SureSelect platform, the GPOL team has developed a suite of affordable, fit-for-purpose cancer genomic assays for both solid and haematological cancers"
The research panel provides excellent performance even with challenging samples like formalin-fixed, paraffin-embedded (FFPE) DNA