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Technical Overviews
A Customer Success Story with the SureSelect Cancer All-In-One Lung and Custom Assays (PDF)

"Many types of cancers are caused by either inherited or de novo genomic abnormalities such as single-nucleotide variants (SNVs), copy number variations (CNVs), and/or chromosomal translocations."

  • Publication Part Number: 5994-3099EN
  • Created: 23 Feb 2021
  • 161 KB
  • PDF
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必威体育登录手机Use of Agilent SureSelect Methyl-Seq to detect high value Differentially Methylated Regions (DMRs) (PDF)

This application note focuses on using open-source software, BSmooth, to detect DMRs in SureSelect Methyl-Seq data and independently validate these high value DMRs

  • Publication Part Number: 5991-5298EN
  • Created: 04 May 2016
  • 737 KB
  • PDF
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Detection of Rare Variants in Degraded FFPE Samples Using the HaloPlex Target Enrichment System Application Note 5991-5479EN (PDF)

必威体育登录手机The Agilent HaloPlex target enrichment system was used to prepare DNA libraries derived from FFPE tissues for NGS sequencing.

  • Created: 28 Aug 2015
  • 627 KB
  • PDF
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采用 RNA ScreenTape 分析法進行 DV200 評估 (PDF)

本技術概述介紹了在 4200 TapeStation 係統上使用高靈敏度 RNA ScreenTape 分析簡化 DV200 的評估。

  • Publication Part Number: 5991-8355ZHCN
  • Created: 09 May 2018
  • 679 KB
  • PDF
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必威体育登录手机利用 Agilent 2100 生物分析儀係統簡化 DV200 評估 (PDF)

必威体育登录手机本技術概述介紹了在 Agilent 2100 生物分析儀係統上使用 DV200 RNA Nano 和 DV200 RNA Pico 分析簡化 DV200 的評估。

  • Publication Part Number: 5991-8287ZHCN
  • Created: 09 May 2018
  • 282 KB
  • PDF
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必威体育登录手机Agilent SureSelect XT Human　Methyl-Seq を用いた1 塩基の解像度でのDNA メチル化定量解析 (PDF)

必威体育登录手机Agilent SureSelect XT Human　Methyl-Seq を用いた1 塩基の解像度でのDNA メチル化定量解析

  • Publication Part Number: 5991-0166JAJP
  • Created: 06 Apr 2013
  • 3 MB
  • PDF

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