Home Failure Case Library Residual Adaptor or Primers After PCR
NGS Library Preparation (NEBNext Ultra II) moderate

Residual Adaptor or Primers After PCR

Symptom
Adaptor or primer peaks visible on Bioanalyzer or similar instrument after PCR amplification, indicating inefficient cleanup or excess reagent usage.
Common Causes
  1. 1 Excess adaptor used during ligation step relative to sample input
  2. 2 Excess PCR primer added or inefficient post-PCR cleanup
  3. 3 SPRI bead cleanup ratio insufficient to remove small adaptor/primer fragments
Solutions
  1. 1 Perform another 0.9X SPRI bead cleanup to remove residual adaptors and primers
  2. 2 Optimize adaptor concentration during ligation based on input amount
  3. 3 Verify correct PCR primer volume is being added according to manual specifications
Related Video (3)
New England Biolabs ★ 95
NEBNext Ultra II DNA Library Prep Protocol
"Directly covers NEBNext Ultra II DNA Library Prep Protocol with step-by-step walkthrough of the exact kit and technique where this failure occurs."
New England Biolabs ★ 78
12 Quick Tips for NGS Library Preparation
"Provides 12 quick tips for NGS library preparation including best practices for adaptor usage and cleanup optimization relevant to preventing residual adaptor peaks."
Illumina ★ 72
How can I tell if I sequenced through the insert? Part 1 | Illumina Video
"Demonstrates how to interpret Bioanalyzer traces to assess library quality and identify primer/adaptor artifacts after PCR amplification."
Source: neb.com ↗
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