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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 Target Enrichment System for Sequencing on Ion Proton Protocol
SureSelect QXT Target Enrichment for Illumina Multiplexed Sequencing Protocol
SureSelect XT Target Enrichment System for the Illumina Platform 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
SureSelect Human All Exon V8 Datasheet: High Performance Exome Built on Advanced and Proven Technology
"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."
SureSelect XT2 Target Enrichment System for Illumina Sequencing Protocol
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.
必威体育登录手机Agilent's streamlined workflow delivers higher precision, less noise and reduced sequencing cost
必威体育登录手机In this Application Note, we present modifications that should be considered when using the Agilent SureSelectXT, SureSelectXT HS, or SureSelectXT low input library preparation protocols for targeted enrichment of viral and bacterial whole genomes...
One assay, all lung cancer-relevant variants in a single DNA workflow
必威体育登录手机Agilent NGS FFPE QC Kit Protocol
SureSelect XT Methyl-Seq Target Enrichment System for Illumina Multiplexed Sequencing Protocol
Next Generation Sequencing Target Enrichment Catalog
This application note focuses on optimizing the SureSelectXT protocol to long-read sequencing and using open-source softwares nanopolish and sniffles to improve the base calling accuracy and detect single nucleotide variants (SNVs) and structural...
The OneSeq 1Mb CNV Backbone + Custom product consists of baits designed to detect CNVs and Loss of Heterozygosity (LOH) genome-wide down to 1Mb and 10Mb resolution