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

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

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In this video, Dr.Madhuri Hegde, a geneticist who runs the global laboratory network for PerkinElmer, discusses the vital role that exome panels play in her lab.

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A webinar on the Glasgow Cancer Core Panel

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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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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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必威体育登录手机Aaron Newman Professor at Stanford University and Co-Founder CiberMed discusses why they have chosen Agilent as a partner.

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Robust NGS results start with high-quality DNA and RNA samples.Learn how to get quick, easy, and flexible sample QC solutions to match your lab's applications and throughput.

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

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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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The SLIMS content management module helps organize your content in SLIMS without the use of spreadsheets or paper.

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This SureDesign tutorial shows you how to create a custom panel targeting genes of interest for specific types of variants, including SNV/indel, CNV and translocation, using the new SureSelect Cancer All-In-One Custom Design workflow in SureDesign.

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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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Learn from genomics expert how exome sequencing impact genetic disorder research.

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Unraveling tumor profiles using exome and transcriptomic sequencing with AI-driven data analysis.

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