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Agilent has solutions for the entire genomics workflow, from the time a sample comes in your lab to informatics to interpret the results
From Extracted DNA to curated variant calls, Agilent has solutions for the entire NGS library prep and analysis workflow. Before spending the time, energy, and money to process NGS samples it’s always necessary to QC the extracted DNA for size, distribution and amount. The Agilent TapeStation systems are fully automated solutions for routine cfDNA sizing analysis.
Automation to meet your needs–with multiple steps and many liquid transfers, NGS library prep is a workflow that can benefit dramatically from being automated.
Magnis NGS Prep system
The Agilent Magnis NGS Prep system is an affordable walk-away automation system which has ready-to-use consumables for hybrid-capture NGS library prep based on SureSelect.
Bravo NGS workstation
The Bravo and AssayMap Bravo are open platform automation systems which deliver higher throughput and hands-free capabilities. Bravo has proven performance and robustness in NGS Sample prep.
SureDesign
SureDesign is a web-based enhanced design
application researchers can use to quickly
generate exceptionally-flexible designs for
high-performance targeted re-sequencing.
The latest SureDesign algorithms ensure that
you get the highest performance
hybridization-capture NGS results.
SureSelect XT HS2 Reagent kits
The SureSelect XT HS2 Reagent kits performs NGS library prep and hybrid-capture enrichment. It includes up to 384 single or dual indexing to enable you to multiplex hundreds of samples.
SureSelect Cancer All-In-One (AIO) assays
SureSelect Cancer All-In-One (AIO) assays are a revolutionary new type of NGS assay. They enable the detection of single nucleotide variants (SNVs), indels, copy number variants (CNVs), and translocations all in in a single research assay.
Agilent has proven qualitative and quantitative QC solutions for your molecular testing needs. The Agilent 4150 and 4200 TapeStations are the ideal systems for fast, reliable and robust NGS library QC.
The Alissa Clinical Informatics Platform
delivers innovative NGS and CGH data analysis,
variant assessment and reporting.
Alissa Align & Call is the scalable NGS data analysis module on the Alissa Clinical Informatics Platform that analyzes raw sequencing data. It seamlessly integrates with Alissa Interpret for clinical-grade variant assessment and reports, reducing workflow complexity and time—from raw data to draft report.
Alissa Interpret enables the standardization and automation of variant triage, review, classification, and reports on clinical NGS and CGH data. Alissa Interpret increases efficiency and diagnostic yield by combining SNV, CNV, and fusion gene data on a single platform and through seamless integration with LIMS and BioIT pipelines.
One source for oligonucleotides and reagents through the entire pipeline, from R&D to commercial therapeutic products
Agilent has extensive experience bringing research discoveries to the clinic. We provide oligonucleotides and technical expertise to cancer researchers throughout the entire research pipeline and at any scale, from initial primer design in the lab all the way to cGMP commercial production. Partner with Agilent and benefit from our industry leading capabilities and experience to meet all your nucleic acid synthesis needs.
In addition to standard oligonucleotides, Agilent has developed SureGuide gRNA – chemically synthesized gRNAs for CRISPR/CAS gene editing. Our ultra-high quality sgRNA for CRISPR are the industry standard, and have few contaminants. Agilent has also developed several unique chemical modifications for sgRNA that improve the efficiency, stability and specificity of sgRNAs in a variety of cell types.
