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必威体育登录手机The Agilent Alissa Reporter platform is an intuitive and streamlined cloud-based NGS secondary analysis software-as-a-service solution.
Protocol for SureSelect XT HS Target Enrichment System
Protocol for SureSelect XT Automated Library Prep and Capture System for Illumina on the NGS Workstation
SureSelect XT Target Enrichment System for the Illumina Platform Protocol
"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
Next Generation Sequencing Target Enrichment Catalog
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
Accelerate the time from design to implementation of your Custom NGS Panels
SureSelect NGS Panels: Customized for Any Application
必威体育登录手机Agilent NGS Design Testing Service