Comprehensive genomic profiling with an NGS pan-cancer panel.Detect somatic alterations (SNVs, indels, CNVs, translocations, de novo gene fusions, TMB, MSI).

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Watch how easily you can analyze your NGS data, interpret variants, report findings, and more with streamlined software tools tailored to your needs.

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This is a webinar by Medicinal Genomics on the SureSelect XT CD StrainSEEK panel.

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必威体育登录手机Seamlessly manage plate sealing, labeling, dilutions, and application protocols for improved precision and cost savings with Agilent's open automation platforms.

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必威体育登录手机Agilent presents the Magnis NGS Prep System and Bravo NGS Platforms, designed to help you generate dependable and high-quality NGS data.

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必威体育登录手机A video about Agilent NGS solutions for lung cancer.

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Learn how easy and simple it is to load the Magnis.The entire process takes less than 10-15 minutes and you can automate your 9.5 hour NGS sample preparation workflow.

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The Bravo easy-to-use interface for instrument setup will empower your technicians with automated NGS workflows used across a range of applications.

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Unlock the full potential of comprehensive genomic profiling to advance precision oncology with the SureSelect Cancer CGP Assay automated on Magnis NGS Prep system.

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必威体育赛事投注See how SureSelect NGS catalog and custom products along with automation for library preparation and target enrichment help you prepare your NGS libraries for sequencing.

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Introducing the SureSelect XT HS2 RNA Reagent Kit: One easy parallel workflow for DNA and RNA to simplify your workflow.

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Running a SureSelect AIO analysis and viewing results

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必威体育登录手机An introduction to Agilent SLIMS, a simple laboratory information management system designed to help your lab run more efficiently.

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This webinar discusses a comparison of several different library preparation methods for whole-exome sequencing of formalin-fixed paraffin embedded (FFPE) tissue.

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Tumor genomic profiling with an NGS pan-cancer panel, plus HRD assessment.Detect somatic alterations (SNVs, indels, CNVs, TLs, de novo gene fusions, TMB, MSI, HRD).

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This is a webinar about the SureSelect XT HS2 DNA and RNA library Preparation kits.

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必威体育登录手机Agilent provides a full suite of SureSelect hybridization capture-based target enrichment products for library preparation and target enrichment.

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

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Alissa Reporter provides downloadable, annotation-ready VCF files from NGS raw data

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