Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • abelhj
    Junior Member
    • Dec 2009
    • 4

    #1

    paired-end question

    Hi,

    I am trying to figure out Solexa paired end read output. Can someone please tell me if my toy example is correct?

    1) One end of DNA is bound to substrate (##). Free end is sequenced in 5'-->3' direction.


    5'
    ------>
    GCCCxxxxxxATTT # ==> GCCC
    CGGGxxxxxxTAAA#




    2) Opposite end of DNA bound to substrate (##). Free end of *complementary* strand sequenced in 5'-->3' direction.


    5'
    ------>
    AAATxxxxxxGGGC# ==> AAAT
    TTTAxxxxxxCCCG #


    So the final output of the Solexa machine would be the pair (GCCC, AAAT) and then a program such as maq would worry about the details of orientation/taking complements. (Or would the pair be (GCCC, TTTA)?)

    Thanks,
    hja
  • ECO
    --Site Admin--
    • Oct 2007
    • 1360

    #2
    For future reference, if you use the [ code ] .... [ /code ] tags it will use a fixed width font and be easier to align!

    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, 10:35 AM
    0 responses
    7 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-06-2026, 07:41 AM
    0 responses
    24 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 08-03-2026, 10:13 AM
    0 responses
    43 views
    0 reactions
    Last Post SEQadmin2  
    Started by SEQadmin2, 07-31-2026, 02:55 AM
    0 responses
    48 views
    0 reactions
    Last Post SEQadmin2  
    Working...