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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.
Presents the use of commercially available ribosomal RNA (rRNA) depletion kits in conjunction with SureSelect XT HS2 RNA reagents for Illumina sequencers.
必威体育登录手机Detection and analysis of methylation by next-generation sequencing (NGS) with the Agilent SureSelect XT HS2 DNA kit.
必威体育登录手机This application note follows the Agilent SureSelectQXT WGS library preparation protocol and demonstrates the performance of 4200 TapeStation system for sample QC.
This study aims to determine how precise targeting of all T cell receptor genes may assist diagnosis and surveillance of T cell malignancies.
必威体育登录手机"Here we present data using the Arima-HiC kit upstream of the Agilent SureSelect XT HS2 target enrichment platform that shows resolution of targeted regions down to 500 bp."
必威体育登录手机The Agilent 4150 TapeStation system performs reliable sample quality control (QC) through various steps of the SureSelect XT HS target enrichment and next-generation sequencing (NGS) library preparation workflow on the Agilent Magnis NGS Prep...
In this application note, we present a condensed and improved workflow for the construction of targeted RNA-sequencing libraries.
必威体育登录手机Agilent's streamlined workflow delivers higher precision, less noise and reduced sequencing cost
Comparisons among Six Different Library Preparation Kits using FFPE Samples for Exome Enrichment Applications
必威体育登录手机Low input cfDNA sequencing and molecular barcode error correction with Agilent SureSelectXT HS technology
必威体育登录手机Describes protocol modifications of the Agilent Strand-Specific RNA Library Prep kit
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...
必威体育登录手机The Agilent SureSelectXT Human Methyl-Seq kit can be used to generate methyl-seq libraries with DNA input amounts as low as 250 ng.