必威体育登录手机A webinar on Agilent Community Designs for Infectious Disease NGS

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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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Here we introduce the SureSelect Cancer All-In-One solution that enables detection of cancer-relevant SNVs, indels, CNVs and translocations with one streamlined DNA workflow, increasing the efficiency and cost-effectiveness of cancer genetic...

• Playing Time: 00:49:40

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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必威体育登录手机Explore the performance and sequencer compatiblity of an Agilent pan-cancer NGS assay with an MGI sequencer, and analyzed using SOPHiA GENETICS software.

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

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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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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Agilent NGS workflow offers a complete solution that can be easily integrated into your lab.In this video, we show how incorporating an the workflow can help your lab.

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

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Running a SureSelect AIO analysis and viewing results

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A webinar on the Glasgow Cancer Core Panel

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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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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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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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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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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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