Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • genlyai
    Member
    • Aug 2009
    • 39

    #1

    Library prep from single-stranded DNA?

    Hi everyone,

    For an application I'm interested in, I would like to sequence libraries on Illumina (or Solid, I guess) starting from material containing both double and single-stranded DNA. If I'm not mistaken, standard library construction will miss single-stranded DNA, right?

    Is anyone aware of a way to get single- and double- (or at least single- alone) stranded material represented in a library?

    Thanks very much for your help!
  • upendra_35
    Senior Member
    • Apr 2010
    • 102

    #2
    Please refer this paper for more on strand specific sequencing

    Comment

    • josdegraaf
      Member
      • Mar 2010
      • 33

      #3

      Comment

      • genlyai
        Member
        • Aug 2009
        • 39

        #4
        Thanks to both of you. To clarify, I'm not interested in strand-specific information, as such, but just in generating libraries that would include DNA that starts off as single-stranded.

        Upendra, I'm not sure I see how the paper you posted will help, but maybe I'm just missing it.

        Jos, your reference claims that single-stranded cDNA will make it into a library even if you don't do anything special. The proposed mechanism is through poorly complementary double-stranded regions being processed to ligatable ends during the blunting step. This might well be useful to me, but the paper lacks info about how efficient the process is and what biases it introduces. Does anyone have any insight into this?

        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, 08-13-2026, 12:22 PM
        0 responses
        20 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-11-2026, 10:35 AM
        0 responses
        17 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-06-2026, 07:41 AM
        0 responses
        32 views
        0 reactions
        Last Post SEQadmin2  
        Started by SEQadmin2, 08-03-2026, 10:13 AM
        0 responses
        50 views
        0 reactions
        Last Post SEQadmin2  
        Working...