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Bring comprehensive genomic profiling in-house today

No matter your sample throughput, Agilent has cancer genomic profiling solutions for you. Unlock the most advanced NGS testing tools in precision oncology with automated sample QC, fully walkaway NGS library preparation automation, catalog and custom NGS target enrichment panels designed with your biomarkers in mind, and integrated bioinformatics tools to analyze your genomic data.

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Learn about Agilent’s pathology workflow solutions

Rapid NGS turnaround time with Magnis automation

Discover how the Glasgow Precision Oncology Laboratory leverages the walkaway Agilent MagnisDx NGS Prep system to achieve a three-day turnaround time in routine NGS testing.

MagnisDx NGS Prep system is a CE-IVD instrument.

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NGS reagents for comprehensive cancer biomarkers

SureSelect cancer genomic profiling solutions enable high-sensitivity detection of somatic SNVs, indels, CNVs, and translocations in a single assay, supporting low-input DNA and FFPE samples.

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Transcriptomics for precision medicine

A study published in Nature Medicine demonstrates how transcriptomics can be used to identify optimal drug targets in oncology based on cancer genomic profiling.

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High-quality NGS from low-input FFPE

The Agilent SureSelect XT HS2 DNA reagent kit helps you generate high-quality libraries with as little as 10 ng of input DNA from highly degraded FFPE samples.

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Pathology informatics solutions

The Alissa Informatics platform streamlines NGS secondary and tertiary analysis with intuitive decision support.

Alissa Interpret is a USA Class I Exempt Medical Device, Europe CE IVD, Canada and Australia Class I IVD Device.

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Walk-away NGS automation at your fingertips

With the Magnis NGS Prep System’s walkaway automation, you can reduce your hands-on time from 2.5 hours to only 10-15 minutes for the full SureSelect library preparation and target enrichment workflow. Let Magnis do the work while you spend more time reviewing results and planning next steps.


NGS workflow for lung cancer biopsy

The current paradigm of translational research in cancer is a multi-modal genomic profiling approach focused on SNVs, indels, CNVs and genomic translocations. In this video, learn how Agilent NGS solutions enable an end-to-end workflow for gaining insights from your lung cancer biopsy.


NSCLC analysis with Dr. Marchetti

In this video, Dr. Marchetti from the University of Chieti describes how Agilent reagents, software, and instrumentation work together to achieve a high degree of specificity and sensitivity in detecting mutations in non-small cell lung cancer.




Unless otherwise stated, all products are For Research Use Only. Not for use in diagnostic procedures.

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