Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • cplinka
    Junior Member
    • Oct 2020
    • 2

    #1

    NGS library enrichment question

    I have a Hi-C library with P5 and P7 adapters. I would like to enrich for fragments containing a locus-of-interest by capture and extension with a biotinylated bait primer, and then amplification with a nested primer and either of the P5/P7 adapters.

    Is is practical to add another sequencing primer adapter to the nested primer, so that I can have the new, enriched library paired-end sequenced? Or will I realistically have to clone the products from the enriched library?

    I apologize for being new to NGS, and thanks in advance for any advice!
  • nucacidhunter
    Jafar Jabbari
    • Jan 2013
    • 1250

    #2
    It would be more cost effective to add adapter sequences to the nested primer for sequencing on cheapest Illumina flow cell.

    Comment

    • cplinka
      Junior Member
      • Oct 2020
      • 2

      #3
      But if the library already has P5 and P7 adapters, what adapter could I add to the nested primer?

      Also, thank you for your response!
      Last edited by cplinka; 10-06-2020, 10:24 AM.

      Comment

      • nucacidhunter
        Jafar Jabbari
        • Jan 2013
        • 1250

        #4
        If you add a PCR handle to 5’ end of probe and then amplify captured target with P5 or P7 primer and the handle primer followed by nested primer containing the other adapter sequences, there will be very small residues of initial library.

        Comment

        Latest Articles

        Collapse

        • SEQadmin2
          Beyond CRISPR/Cas9: Understand, Choose, and Use the Right Genome Editing Tool
          by SEQadmin2



          CRISPR/Cas9 sparked the gene editing revolution for both research and therapeutics.1 But this system still showed severe issues that limited its applications. The most prominent were the heavy reliance on PAM sequences, delivery limitations, double-stranded breaks that prompt unintended edits and cell death, and editing inefficiency (both in targeting and in knock-in reliability).

          Despite this, “CRISPR helped turn genome editing from a specialized technique into
          ...
          07-31-2026, 11:01 AM
        • SEQadmin2
          Proteomic Platforms: How to Choose the Right Analytical Strategy to Improve Detection and Clinical Applications
          by SEQadmin2


          Proteomics platforms are evolving rapidly, with advances in mass spectrometry and affinity-based approaches expanding what researchers can detect and at what scale. As the field moves toward deeper proteome coverage and clinical applications, scientists face an increasingly complex landscape of tools. This article will explore how researchers are navigating these choices to find the right platform for their work.

          The systematic characterization of the human proteome has
          ...
          07-20-2026, 11:48 AM

        ad_right_rmr

        Collapse

        News

        Collapse

        Topics Statistics Last Post
        Started by SEQadmin2, Yesterday, 12:22 PM
        0 responses
        12 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-11-2026, 10:35 AM
        0 responses
        14 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        31 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        49 views
        0 reactions
        Last Post SEQadmin2  
        Working...