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必威体育登录手机This application note introduces a method for target capture (long-read) sequencing using the Agilent SureSelect XT HS2 target enrichment system with some protocol modifications.
User Guide for SureSelect Cancer CGP Assay and SureSelect Cancer Tumor-specific Assays.
This application note describes the performance characteristics of the SureSelect CD Tissue panel for profiling both FF and FFPE tissue samples with a CiberMed digital cytometry software solution iSort.
Here we demonstrate robust, accurate, and reproducible enumeration of immune cell subsets from 36 whole blood samples using SureSelect XT HS2 RNA sequencing combined with CiberMed's iSort digital cytometry.
Provides SureSelect XT HS2 index sequences in Excel format.Click the Sequence Resource link to download the .xlsx file to your local device (typically Downloads folder).
Protocol for SureSelect XT HS2 DNA Library Preparation and Overnight-Hyb, pre-capture pooling Target Enrichment for Illumina paired-end multiplexed sequencing.
Protocol for SureSelect XT HS2 DNA Library Preparation and Overnight-Hyb, post-capture pooling Target Enrichment for Illumina paired-end multiplexed sequencing.
必威体育登录手机Protocol for SureSelect XT Low Input Target Enrichment System, Automated using the Agilent NGS Workstation Option B
必威体育登录手机Protocol for SureSelect XT Low Input Target Enrichment System, Automated using the Agilent NGS Bravo Option A
Protocol for SureSelect XT HS Target Enrichment System
Protocol for preparation of dual-indexed libraries using SureSelect XT Low Input Target Enrichment System
Protocol for SureSelect XT Low Input Target Enrichment System
Protocol for SureSelect XT Automated Library Prep and Capture System for Illumina on the NGS Workstation
必威体育登录手机Protocol for SureSelect QXT Automated Target Enrichment for Illumina on the Agilent NGS Workstation Option B
SureSelect QXT Automated Target Enrichment for Illumina Multiplexed Sequencing Protocol (NGS Bravo Option A)
SureSelect Target Enrichment System for Sequencing on Ion Proton Protocol
SureSelect XT Target Enrichment System for the Illumina Platform Protocol
SureSelect QXT Target Enrichment for Illumina Multiplexed Sequencing Protocol
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."