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Protocol for SureSelect XT HS Target Enrichment System
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
One assay, all lung cancer-relevant variants in a single DNA workflow