Agilent Community
Agilent Community
  • User
  • Site
  • Search the Community
  • User
  • Home
  • Technical Areas
    Technical Areas
    • AssayMap
    • Atomic Spectroscopy
    • Automated Electrophoresis
    • Bioreagents
    • Cell Analysis
    • Consumables
    • CrossLab Connect
      CrossLab Connect
      • Service Management
      • Smart Alerts
    • Dissolution
    • Gas Chromatography
    • GC/MS
    • LC/MS
    • Liquid Chromatography
    • Molecular Spectroscopy
    • Sample Preparation
    • Software
      Software
      • Chromatography Software
        OpenLab CDS, OpenLab ChemStation, OpenLab EZChrom
      • Data Management Software
        OpenLab ECM, OpenLab ECM XT, OpenLab Server
      • Mass Spectrometry Software
        Data Analysis, Data Acquisition, Productivity App, WalkUp Software
    • Vacuum
  • Applications Areas
    Applications Areas
    • Basic Research
    • Energy and Chemicals
    • Environmental
    • Food and Agriculture
  • Agilent Knowledge Portal
  • Links
    Links
    • Collection of Support Resources
    • Webinar Notifications
    • Contact Support
    • User Contributions
  • Getting Started
    Community Help and Resources
  • Browse
    Browse
    • People
    • Places
    • Your View
    • Your Community Inbox
Automated Electrophoresis Portal
  • Agilent Knowledge Portal
Automated Electrophoresis Portal
Automated Electrophoresis Articles Peak Fronting in NGS Library Smears on Agilent TapeStation
  • Automated Electrophoresis Articles
  • Automated Electrophoresis Forum
  • More
  • Cancel

Browse the Agilent Knowledge Portal

  • Chromatography
    • Gas Chromatography
    • Liquid Chromatography
  • More
  • Cancel
  • GC/MS
  • More
  • Cancel
  • Spectroscopy
    • Atomic Absorption
    • ICP-OES
  • More
  • Cancel
  • Automated Electrophoresis
  • More
  • Cancel
  • Software and Informatics
    • OpenLab CDS
    • MassHunter
  • More
  • Cancel
  • -Automated Electrophoresis
    • +Bioanalyzer
    • -Tapestation
      • Discrepancy between Agilent RIN and RINᵉ values
      • How to Determine the DV200 of FFPE RNA Samples on the Agilent TapeStation
      • Caught Exception in Agilent 2200 TapeStation Controller Software: Configuration System Failed to Initialize
      • Agilent TapeStation Software Displays a Different ScreenTape Expiration Date
      • Peak Fronting in NGS Library Smears on Agilent TapeStation
      • Agilent 4150 TapeStation Lid does not Close
      • Intensity Loss for 200 nt Ladder Peak in the Agilent TapeStation RNA Assays
      • How to Export Agilent TapeStation Logs
    • +Parallel Electrophoresis

Peak Fronting in NGS Library Smears on Agilent TapeStation

Created by Jasmin Manck-Goetzenberger Jasmin Manck-Goetzenberger over 1 year ago | Last modified by Geoff Pettitt Geoff Pettitt 11 months ago

This Information Applies To: 2200/4200/4250 TapeStation systems, TapeStation D1000 ScreenTape assay, TapeStation High Sensitivity D1000 ScreenTape assay, TapeStation analysis software


Issue:

A sharp peak appears at the lower end of the NGS library smear in Agilent TapeStation D1000 ScreenTape and High Sensitivity D1000 ScreenTape assays (see Figure 1).

 

Figure 1. Region analysis (blue borders) of an NGS library smear. The red arrow indicates the peak fronting.


Resolution: 

Peak fronting is an electrophoretic artifact. The cause is a concentration-dependent stacking effect on D1000 and High Sensitivity D1000 ScreenTape assays. In certain circumstances, some fragments might show a similar mobility and stack together, forming a distinct peak within the smear. It is more obvious in low-input libraries with medium to low concentrations. It does not represent a contamination in the library. Potential causes include factors such as the sample resuspension buffer, sample smear size, and concentration range. Therefore, rerunning the samples on the same ScreenTape kit will not help as the effect is inherent of the sample.

Peak fronting does not affect the overall quantification as long as the smear is correctly integrated (see region included in Figure 1). However, the sizing might be slightly shifted and therefore the molarity might be marginally altered as well. Nevertheless, quantification and sizing results are usually meeting the kit accuracy and precision specifications. Peak fronting typically does not alter results significantly, as long as the samples are meeting kit sizing and concentration specifications (see also Quick Guides and for smear specifications technical overview):

Kit Sizing range Quantification range (DNA fragments) Quantification range (DNA smears)
D1000 35–1000 bp 0.1–50 ng/µl 5–100 ng/µl
High Sensitivity D1000 35–1000 bp 10–1000 pg/µl 0.5–15 ng/µl

Please use the following search terms to find more information about this and other NGS library phenomena in the Agilent Information Center (AIC) on your PC: TapeStation Analysis in the SureSelect and HaloPlex Workflow.

Root cause: 
Concentration-dependent stacking effect

 Tip 
Learn how to effectively operate your Agilent D1000 and High Sensitivity D1000 ScreenTape assays:
Agilent D1000 ScreenTape Assay for TapeStation Systems Quick Guide
Agilent High Sensitivity D1000 ScreenTape Assay for TapeStation Systems Quick Guide

For Research Use Only. Not for use in diagnostic procedures.

PR7000-8075


  • 2200 TapeStation
  • TapeStation Software
  • Troubleshooting
  • Data Analysis
  • 4200 TapeStation
  • 4150 TapeStation
  • tapestation
  • TapeStation Data Analysis Software
  • ScreenTapes and Reagents
  • Share
  • History
  • More
  • Cancel
Was this helpful?
  • Yes
  • No
Thank you for your feedback!

Agilent Community Feedback

Agilent Community Feedback

×
We are glad this was helpful! We are sorry this was not helpful. If you still need assistance please create a community post or contact support. To help us improve, please provide any additional feedback. For full details of how we will treat your information, please view our privacy policy.
Submit Cancel
Submit Cancel

Contact Agilent Support

 Still Need Assistance?

 Contact Agilent Support >

Related
Recommended for you
Privacy Statement
Terms of Use
Contact Us
Site Help