Unconfigured Ad

Collapse
X
 
  • Time
  • Show
Clear All
new posts
  • jlove
    Member
    • Apr 2011
    • 49

    #1

    P5/P7 Flowcell Oligos

    I apologize if this has been hashed out already, but I cannot seem to find any definitive documentation which describes whether the flowcell oligos are P5 and P7, or the complements. I know Illumina considers this information proprietary so it's not immediately obvious to me. I am wondering whether or not an excess of free P5 and P7 custom PCR primer (not dimer) would bind to the flowcell. I understand why dimers (which amplify and thus contain both P5/complement to P5, etc) would bind to the flowcell, but what about just these oligos?

    My primers are:
    SLXP5_PCR - AATGATACGGCGACCACCGAG
    SLXP7_PCR - CAAGCAGAAGACGGCATACGAG

    Anybody have a good, clear resource on this?

    Thanks in advance!
  • nucacidhunter
    Jafar Jabbari
    • Jan 2013
    • 1250

    #2
    Those oligos will not bind to flow cell oligo lawn but may bind to library strands reducing their effective concentration resulting in under clustering. Flow cell oligos for SE and PE flow cells are as following:

    PE: 5’-PS-TTTTTTTTTT---------AATGATACGGCGACCACCGAGAUCTACAC-3’
    SE: 5’-PS-TTTTTTTTTT-(diol)3-AATGATACGGCGACCACCGA-3

    PE: 5’-PS-TTTTTTTTTTCAAGCAGAAGACGGCATACGAGoxoAT-3’
    SE: 5’-PS-TTTTTTTTTTCAAGCAGAAGACGGCATACGA-3

    Comment

    • jlove
      Member
      • Apr 2011
      • 49

      #3
      This is very handy, thank you! May I ask how you figured out these sequences?
      Jen


      Originally posted by nucacidhunter View Post
      Those oligos will not bind to flow cell oligo lawn but may bind to library strands reducing their effective concentration resulting in under clustering. Flow cell oligos for SE and PE flow cells are as following:

      PE: 5’-PS-TTTTTTTTTT---------AATGATACGGCGACCACCGAGAUCTACAC-3’
      SE: 5’-PS-TTTTTTTTTT-(diol)3-AATGATACGGCGACCACCGA-3

      PE: 5’-PS-TTTTTTTTTTCAAGCAGAAGACGGCATACGAGoxoAT-3’
      SE: 5’-PS-TTTTTTTTTTCAAGCAGAAGACGGCATACGA-3

      Comment

      • nucacidhunter
        Jafar Jabbari
        • Jan 2013
        • 1250

        #4
        I have got it somewhere from a google search years ago, so the base modification may not be applicable to two colour chemistry or patterned flow cells. I think the sequences are still the same as old and new adapters share flow cell binding motives and when library fragments are shorter than cycle number a long stretch of A after adapter sequences are observed that are complementary to T homopolymer.

        Comment

        • darklight
          Junior Member
          • Sep 2021
          • 3

          #5
          Originally posted by jlove View Post
          This is very handy, thank you! May I ask how you figured out these sequences?
          Jen
          This is very helpful. May I ask what does oxo stand for in the sequence?

          Comment

          • nucacidhunter
            Jafar Jabbari
            • Jan 2013
            • 1250

            #6
            I is oxoadenine (oxoA).

            Comment

            • darklight
              Junior Member
              • Sep 2021
              • 3

              #7
              Originally posted by nucacidhunter View Post
              I is oxoadenine (oxoA).
              Thank you!

              Comment

              Latest Articles

              Collapse

              • SEQadmin2
                Multiomic Liquid Biopsy: What DNA/RNA Panels Reveal That DNA Alone Can’t
                by SEQadmin2



                Tumors contain complex mixtures of cell populations that evolve in response to treatment and host-specific factors. Tissue biopsies provide only static snapshots of a tumor’s state. But what if we could follow that evolution over time using a minimally invasive technique?

                Liquid biopsies can detect tumor-derived material circulating in the bloodstream, providing a way to study treatment response, detect emerging resistance, and discover new biomarkers. Circulating
                ...
                10-14-2026, 09:55 AM
              • SEQadmin2
                New Genomics Technologies Take Aim at Long-Standing Limits
                by SEQadmin2


                Researchers using sequencing and genomics tools often have to make trade-offs. They can choose between speed or scale, short reads or long-range information, or targeted panels or a view of the whole transcriptome. New technologies that have been released this year are built to address those tough choices.

                We asked six companies the same four questions to learn about their latest products. The new technologies bring a lot to the table, including rethinking sequencing
                ...
                09-28-2026, 10:25 AM

              ad_right_rmr

              Collapse

              News

              Collapse

              Topics Statistics Last Post
              Started by SEQadmin2, 10-15-2026, 10:52 AM
              0 responses
              13 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-14-2026, 05:39 AM
              0 responses
              21 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-13-2026, 09:56 AM
              0 responses
              19 views
              0 reactions
              Last Post SEQadmin2  
              Started by SEQadmin2, 10-09-2026, 11:14 AM
              0 responses
              27 views
              0 reactions
              Last Post SEQadmin2  
              Working...