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Somatic and Germline sequencing of SureSelect Libraries on the Element AVITI System
Library Preparation Performance on the Magnis NGS Prep System with Reagent and Protocol Updates
SureSelect Human All Exon V8 Datasheet: High Performance Exome Built on Advanced and Proven Technology
必威体育登录手机"The Agilent SureSelect XT HS2 RNA Reagent Kit is an advanced solution for targeted RNA-Seq.It is optimized for low-input, formalin-fixed paraffin-embedded (FFPE) samples, a critical sample type for translational cancer research."
必威体育登录手机The Agilent Magnis NGS Prep System (Figure 1) produces sequencing-ready libraries compatible with Illumina platforms.It is comprised of an instrument, reagents, and pre-configured protocols.The system is fully automated to deliver eight libraries...
Alissa Align & Call ushers in the next generation of NGS data analysis, delivering bioinformatic accuracy and speed, from raw data to draft report
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.
One assay, all lung cancer-relevant variants in a single DNA workflow
NGS with Molecular Barcodes Uncovers Somatic Mosaicism
A fast, simple and reliable enzymatic fragmentation workflow for NGS library preparation
Alissa Interpret | Research, the next evolution of Cartagenia Bench, allows clinical research labs to efficiently triage, curate and report genomic variants.
| Portuguese (Brazil) | Complete (PDF) |
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| Spanish (Mexico) | Complete (PDF) |
A list of publications that cite HaloPlexHS
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
必威体育登录手机Agilent SureSelectXT Human Methyl-Seq for the Quantitative Analysis of DNA Methylation with Single-Base Resolution